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MC-(β-Ala)-PABC-(β-D-GlcUA)-amide-PEG1-CH2-CC-885

" in MedChemExpress (MCE) Product Catalog:

By Targets:	ADC Linker (23) Antibody-Drug Conjugates (ADCs) (1) Apoptosis (1) Autophagy (1) Biochemical Assay Reagents (1) DNA Alkylator/Crosslinker (1) Drug-Linker Conjugates for ADC (2) E3 Ligase Ligand-Linker Conjugates (11) Ligands for E3 Ligase (4) PROTAC Linkers (59) PROTAC-Linker Conjugates for PAC (1) Toll-like Receptor (TLR) (3) Topoisomerase (2)
By Research Areas:	Cancer (96) Cardiovascular Disease (1) Inflammation/Immunology (5) Metabolic Disease (2)
Click Chemistry:	ADC Synthesis (13) TCO (3) DBCO (6) PROTAC Synthesis (19) BCN (3) Azide (8) Alkynes (15)

100

Inhibitors & Agonists

Biochemical Assay Reagents

MCE Kits

Natural
Products

Recombinant Proteins

Antibodies

Click Chemistry

Targets Recommended: FAAH

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-160497

*MC-(β-Ala)-PABC-(β-D-GlcUA)-amide-PEG1-CH2-CC-885*	PROTAC-Linker Conjugates for PAC	Cancer
MC-(β-Ala)-PABC-(β-D-GlcUA)-amide-PEG1-CH2-CC-885 (Comp Ie) is a neodegrader conjugate, can be used in the synthesis of antibody neoDegrader conjugate (AnDC) ^[1].

HY-145448

MC-VC-PABC-amide-PEG1-CH2-CC-885

Antibody-Drug Conjugates (ADCs) Cancer

MC-VC-PABC-amide-PEG1-CH2-CC-885 is a neodegrader ^[1].

*MC-VC-PABC-amide-PEG1-CH2-CC-885*	Antibody-Drug Conjugates (ADCs)	Cancer
MC-VC-PABC-amide-PEG1-CH2-CC-885 is a neodegrader ^[1].

HY-130923

*BCN-PEG1-Val-Cit-PABC-OH*	ADC Linker	Cancer
BCN-PEG1-Val-Cit-PABC-OH is a cleavable 1 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1]. BCN-PEG1-Val-Cit-PABC-OH is a click chemistry reagent, it contains a BCN group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.

HY-130966

*TCO-PEG1-Val-Cit-PABC-OH*	ADC Linker	Cancer
TCO-PEG1-Val-Cit-PABC-OH is a cleavable 1 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1]. TCO-PEG1-Val-Cit-PABC-OH is a click chemistry reagent, it contains a TCO group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing Tetrazine groups.

HY-136100

*TCO-PEG1-Val-Cit-PABC-PNP*	ADC Linker	Cancer
TCO-PEG1-Val-Cit-PABC-PNP is a cleavable 1 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1]. TCO-PEG1-Val-Cit-PABC-PNP is a click chemistry reagent, it contains a TCO group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing Tetrazine groups.

HY-130944

Mal-PEG1-Val-Cit-PABC-OH

ADC Linker Cancer

Mal-PEG1-Val-Cit-PABC-OH is a cleavable 1 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1].

*Mal-PEG1-Val-Cit-PABC-OH*	ADC Linker	Cancer
Mal-PEG1-Val-Cit-PABC-OH is a cleavable 1 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1].

HY-136105

*Azido-PEG1-Val-Cit-PABC-PNP*	ADC Linker	Cancer
Azido-PEG1-Val-Cit-PABC-PNP is a cleavable 1 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1]. Azido-PEG1-Val-Cit-PABC-PNP is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.

HY-136137

*Azide-PEG1-Val-Cit-PABC-OH*	ADC Linker	Cancer
Azide-PEG1-Val-Cit-PABC-OH is a cleavable 1 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1]. Azide-PEG1-Val-Cit-PABC-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.

HY-147095

*Val-Ala-PABC-Exatecan*	Drug-Linker Conjugates for ADC Topoisomerase	Cancer
Val-Ala-PABC-Exatecan is a Drug-Linker Conjugates for ADC，consiting of a cleavable Tesirine linker (Val-Ala-PABC) and Exatecan (topoisomerase I inhibitor，HY-13631). Val-Ala-PABC-Exatecan can be used for ADC molecues synthesis，such as Mal-PEGn-amide-va-Exatecan ^[1].

HY-147095A

*Val-Ala-PABC-Exatecan trifluoroacetate*	Drug-Linker Conjugates for ADC Topoisomerase	Cancer
Val-Ala-PABC-Exatecan trifluoroacetate is a Drug-Linker Conjugates for ADC, consiting of a cleavable Tesirine linker (Val-Ala-PABC) and Exatecan (topoisomerase I inhibitor, HY-13631). Val-Ala-PABC-Exatecan trifluoroacetate can be used for ADC molecues synthesis, such as Mal-PEGn-amide-va-Exatecan ^[1].

HY-131890

*VH032 amide-PEG1-acid*	DNA Alkylator/Crosslinker E3 Ligase Ligand-Linker Conjugates	Cancer
VH032 amide-PEG1-acid (linker 10) is a *VHL-1* alkyl linker that can be used to bind CDK4/6 ligands (PI) and degradation/destruction tags (EL) (e.g.,E3 ligase ligands) ^[1].

HY-N12840

Logmalicid B

Others Metabolic Disease

Logmalicid B is an iridoid glycoside compound that can be isolated from Cornus officinalis and can be used in diabetes research ^[1].
HY-129361

Fmoc-Ala-Ala-Asn-PABC-PNP

ADC Linker Cancer

Fmoc-Ala-Ala-Asn-PABC-PNP is a peptide cleavable ADC linker ^[1].

Logmalicid B	Others	Metabolic Disease
Logmalicid B is an iridoid glycoside compound that can be isolated from Cornus officinalis and can be used in diabetes research ^[1].

*Fmoc-Ala-Ala-Asn-PABC-PNP*	ADC Linker	Cancer
Fmoc-Ala-Ala-Asn-PABC-PNP is a peptide cleavable ADC linker ^[1].

HY-136304

*NHS-PEG1-SS-PEG1-NHS*	Biochemical Assay Reagents	Cardiovascular Disease Metabolic Disease Cancer
NHS-PEG1-SS-PEG1-NHS is a reversible linker for biomacromolecule link with active small molecule. NHS-PEG1-SS-PEG1-NHS can be used in proteins liposomes or nanoparticles ^[1].

HY-145255

*Tri(TLR4-IN-C34-C2-amide-C3-amide-PEG1)-amide-C3-COOH*	PROTAC Linkers Toll-like Receptor (TLR)	Inflammation/Immunology
Tri(TLR4-IN-C34-C2-amide-C3-amide-PEG1)-amide-C3-COOH is a linker that incorporates TLR4 inhibitor TLR4-IN-C34. TLR4-IN-C34 inhibits TLR4 in enterocytes and macrophages, and reduces systemic inflammation in mouse models of endotoxemia and necrotizing enterocolitis ^[1].

HY-140109

*Propargyl-PEG1-SS-PEG1-acid*	ADC Linker	Cancer
Propargyl-PEG1-SS-PEG1-acid is a cleavable 2 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1]. Propargyl-PEG1-SS-PEG1-acid is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-145253

*Tri(TLR4-IN-C34-C2-amide-PEG1)-amide-C3-COOH*	PROTAC Linkers Toll-like Receptor (TLR)	Inflammation/Immunology
Tri(TLR4-IN-C34-C2-amide-PEG1)-amide-C3-COOH is a linker that incorporates TLR4 inhibitor TLR4-IN-C34. TLR4-IN-C34 inhibits TLR4 in enterocytes and macrophages, and reduces systemic inflammation in mouse models of endotoxemia and necrotizing enterocolitis ^[1].

HY-145254

*Tri(TLR4-IN-C34-PEG2-amide-PEG1)-amide-C3-COOH*	Toll-like Receptor (TLR)	Inflammation/Immunology
Tri(TLR4-IN-C34-PEG2-amide-PEG1)-amide-C3-COOH is a linker that incorporates TLR4 inhibitor TLR4-IN-C34. TLR4-IN-C34 inhibits TLR4 in enterocytes and macrophages, and reduces systemic inflammation in mouse models of endotoxemia and necrotizing enterocolitis ^[1].

HY-140111

*Propargyl-PEG1-SS-PEG1-propargyl*	ADC Linker	Cancer
Propargyl-PEG1-SS-PEG1-propargyl is a cleavable 2 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1]. Propargyl-PEG1-SS-PEG1-propargyl is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-140110

*Propargyl-PEG1-SS-PEG1-PFP ester*	ADC Linker	Cancer
Propargyl-PEG1-SS-PEG1-PFP ester is a cleavable 1 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1]. Propargyl-PEG1-SS-PEG1-PFP ester is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-130690

*Propargyl-PEG1-SS-PEG1-C2-Boc*	ADC Linker PROTAC Linkers	Cancer
Propargyl-PEG1-SS-PEG1-C2-Boc is a Alkyl/ether-based PROTAC linker can be used in the synthesis of PROTACs. Propargyl-PEG1-SS-PEG1-C2-Boc is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1]. Propargyl-PEG1-SS-PEG1-C2-Boc is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-136008A

*(S,R,S)-AHPC-PEG1-NH2 dihydrochloride* VH032-PEG1-NH2 dihydroCHloride	E3 Ligase Ligand-Linker Conjugates	Cancer
(S,R,S)-AHPC-PEG1-NH2 (VH032-PEG1-NH2) dihydrochloride incorporates a VHL ligand for the E3 ubiquitin ligase and a PROTAC linker. (S,R,S)-AHPC-PEG1-NH2 dihydrochloride can be used to design PROTACs ^[1].

HY-161128

*Lenalidomide 4'-PEG1-amine dihydrochloride*	Ligands for E3 Ligase	Cancer
Lenalidomide 4'-PEG1-amine dihydrochloride is the Lenalidomide-based Cereblon ligand used in the recruitment of CRBN protein. Lenalidomide 4'-PEG1-amine dihydrochloride can be connected to the ligand for protein by a linker to form PROTAC ^[1].

HY-126960

*Mal-PEG1-acid*	PROTAC Linkers ADC Linker	Inflammation/Immunology Cancer
Mal-PEG1-acid is is a non-cleavable 1 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Mal-PEG1-acid is a PEG-based PROTAC linker can be used in the synthesis of PROTACs.

HY-126886

*Mal-PEG1-NHS ester*	ADC Linker PROTAC Linkers	Cancer
Mal-PEG1-NHS ester is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Mal-PEG1-NHS ester is PEG-based PROTAC linker that can be used in the synthesis of PROTACs.

HY-128847

Bis-PEG1-C-PEG1-CH2COOH

PROTAC Linker 26
PROTAC Linkers Cancer

Bis-PEG1-C-PEG1-CH2COOH (PROTAC Linker 26) is a PEG-based PROTAC linker can be used in the synthesis of PROTACs ^[1].

*Bis-PEG1-C-PEG1-CH2COOH* PROTAC Linker 26	PROTAC Linkers	Cancer
Bis-PEG1-C-PEG1-CH2COOH (PROTAC Linker 26) is a PEG-based PROTAC linker can be used in the synthesis of PROTACs ^[1].

HY-140280

DBCO-PEG1	PROTAC Linkers	Cancer
DBCO-PEG1 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. DBCO-PEG1 is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.

HY-133138

*Pomalidomide-PEG1-azide*	E3 Ligase Ligand-Linker Conjugates	Cancer
Pomalidomide-PEG1-azide is a E3 ligase lgand-linker conjugate. Pomalidomide-PEG1-azide incorporates the Pomalidomide based cereblon ligand and a linker.?Pomalidomide-PEG1-azide?can be used to design a?PROTAC BRD4 Degrader-1 (HY-133131) ^[1]. Pomalidomide-PEG1-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.

HY-133139

*Lenalidomide-PEG1-azide*	E3 Ligase Ligand-Linker Conjugates	Cancer
Lenalidomide-PEG1-azide is a E3 ligase lgand-linker conjugate. Lenalidomide-PEG1-azide incorporates the Lenalidomide based cereblon ligand and a linker.?Lenalidomide-PEG1-azide?can be used to design a PROTAC BRD4 Degrader-2 (HY-133136) ^[1]. Lenalidomide-PEG1-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.

HY-161133

*Lenalidomide 4'-PEG1-azide*	E3 Ligase Ligand-Linker Conjugates	Cancer
Lenalidomide 4'-PEG1-azide (Compound 4g) is a lenalidomide-derived azide. Lenalidomide 4'-PEG1-azide incorporates the Lenalidomide based cereblon ligand and a linker. Lenalidomide 4'-PEG1-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups. ^[1].

HY-140265

*DBCO-PEG1-acid*	PROTAC Linkers	Cancer
DBCO-PEG1-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. DBCO-PEG1-acid is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.

HY-132252

Mal-PEG8-Val-Ala-PABC

ADC Linker Cancer

Mal-PEG8-Val-Ala-PABC is a cleavable Tesirine linker used in the synthesis of Tesirine, a agent-linker conjugate for ADC ^[1].

Mal-PEG8-Val-Ala-PABC	ADC Linker	Cancer
Mal-PEG8-Val-Ala-PABC is a cleavable Tesirine linker used in the synthesis of Tesirine, a agent-linker conjugate for ADC ^[1].

HY-136008

*(S,R,S)-AHPC-PEG1-NH2* VH032-PEG1-NH2	E3 Ligase Ligand-Linker Conjugates	Cancer
(S,R,S)-AHPC-PEG1-NH2 (VH032-PEG1-NH2) is a synthesized E3 ligase ligand-linker conjugate that incorporates the VH032 based VHL ligand and a linker used in PROTAC technology ^[1].

HY-140038

Bis-propargyl-PEG1	PROTAC Linkers	Cancer
Bis-propargyl-PEG1 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. Bis-propargyl-PEG1 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-140281

DBCO-C-PEG1	PROTAC Linkers	Cancer
DBCO-C-PEG1 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. DBCO-C-PEG1 is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.

HY-130425

Bromo-PEG1-acid

PROTAC Linkers Cancer

Bromo-PEG1-acid is a PEG-based PROTAC linker can be used in the synthesis of PROTACs ^[1].
HY-23166

Bis-PEG1-acid

PROTAC Linkers Cancer

Bis-PEG1-acid is a PEG-based PROTAC linker can be used in the synthesis of PROTACs ^[1].
HY-140000

Methylamino-PEG1-acid

PROTAC Linkers Cancer

Methylamino-PEG1-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1].

*Bromo-PEG1-acid*	PROTAC Linkers	Cancer
Bromo-PEG1-acid is a PEG-based PROTAC linker can be used in the synthesis of PROTACs ^[1].

*Bis-PEG1-acid*	PROTAC Linkers	Cancer
Bis-PEG1-acid is a PEG-based PROTAC linker can be used in the synthesis of PROTACs ^[1].

*Methylamino-PEG1-acid*	PROTAC Linkers	Cancer
Methylamino-PEG1-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1].

HY-140032

*Alkyne-ethyl-PEG1-Boc* Alkyne-ethyl-PEG1-t-butyl ester	PROTAC Linkers	Cancer
Alkyne-ethyl-PEG1-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. Alkyne-ethyl-PEG1-Boc is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-140154

Methylamino-PEG1-Boc

Methylamino-PEG1-t-butyl ester
PROTAC Linkers Cancer

Methylamino-PEG1-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1].

*Methylamino-PEG1-Boc* Methylamino-PEG1-t-butyl ester	PROTAC Linkers	Cancer
Methylamino-PEG1-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1].

HY-140056

*Aminooxy-PEG1-propargyl*	PROTAC Linkers	Cancer
Aminooxy-PEG1-propargyl is a PEG-based PROTAC linker can be used in the synthesis of PROTACs ^[1]. Aminooxy-PEG1-propargyl is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-140064

*Propargyl-PEG1-acrylate*	PROTAC Linkers	Cancer
Propargyl-PEG1-acrylate is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. Propargyl-PEG1-acrylate is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-140271

*DBCO-PEG1-NHS ester*	PROTAC Linkers	Cancer
DBCO-PEG1-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. DBCO-PEG1-NHS ester is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.

HY-140282

*DBCO-PEG1-amine*	PROTAC Linkers	Cancer
DBCO-PEG1-amine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. DBCO-PEG1-amine is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.

HY-138334

*Propargyl-PEG1-THP*	PROTAC Linkers	Cancer
Propargyl-PEG1-THP is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. Propargyl-PEG1-THP is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-W096146

*Propynyl-PEG1-Ac*	PROTAC Linkers	Cancer
Propynyl-PEG1-Ac is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. Propynyl-PEG1-Ac is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-W096134

Benzyloxy-C5-PEG1

PROTAC Linkers Cancer

Benzyloxy-C5-PEG1 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1].

HY-126513

*Propargyl-PEG1-NHS ester*	ADC Linker	Cancer
Propargyl-PEG1-NHS ester is a nonclaevable 1-unit PEG linker for antibody-agent-conjugation (ADC). Propargyl-PEG1-NHS ester is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-140026

*Propargyl-PEG1-Boc*	PROTAC Linkers	Cancer
Propargyl-PEG1-Boc is an alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. Propargyl-PEG1-Boc is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-140407

Bis-aminooxy-PEG1

PROTAC Linkers Cancer

Bis-aminooxy-PEG1 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1].

Species:	Human (4) Mouse (1)
Tag:	His (4) GST (1)
Source:	HEK293 (2) E. coli Cell-free (1) E. coli (2)

Cat. No.	Compare	Product Name	Species	Source

HY-P76272

	CNDP1 Protein, Mouse (HEK293, His) Beta-Ala-His dipeptidase; CNDP dipeptidase 1; Cn1	Mouse	HEK293
	The CNDP1 protein is critical in cellular processes and catalyzes the hydrolysis of the Xaa-His dipeptide, with the highest activity against carnosine and anserine. This enzyme specificity highlights the critical role of CNDP1 in regulating the breakdown of specific dipeptides, especially those involving histidine. CNDP1 Protein, Mouse (HEK293, His) is the recombinant mouse-derived CNDP1 protein, expressed by HEK293 , with C-His labeled tag. The total length of CNDP1 Protein, Mouse (HEK293, His) is 492 a.a., with molecular weight of ~57 KDa.

HY-P71641

	IFIH1 Protein, Human (His) CADM-140 autoantigen; Clinically amyopathic dermatomyositis autoantigen 140kDa; DEAD/H (Asp Glu Ala Asp/His) box polypeptide; DEAD/H box polypeptide; Helicard; Helicase with 2 CARD domains; Hlcd; MDA-5	Human	E. coli
	The IFIH1 protein is an innate immune receptor that detects viral nucleic acids and triggers an antiviral response. IFIH1 is critical for type I interferon induction and recognizes ligands such as mRNA lacking 2'-O-methylation and long double-stranded RNA. IFIH1 Protein, Human (His) is the recombinant human-derived IFIH1 protein, expressed by E. coli , with N-6*His labeled tag. The total length of IFIH1 Protein, Human (His) is 326 a.a., with molecular weight of ~41.5 kDa.

HY-P7740

	Carnosine Dipeptidase 1/CNDP1 Protein, Human (HEK293, His) rHuCarnosine Dipeptidase 1, His; Beta-Ala-His Dipeptidase; CNDP Dipeptidase 1; Carnosine Dipeptidase 1; Glutamate Carboxypeptidase-Like Protein 2; Serum Carnosinase; CNDP1; CN1; CPGL2	Human	HEK293
	Carnosine Dipeptidase 1 Protein, Human (HEK293, His) is a human carnosine dipeptidase 1 protein with a his-flag, expressed in HEK293 cells. Carnosine Dipeptidase 1 is a member of the M20 metalloprotease family, encoded by the CNDP1 gene.

HY-P702276

	FAAH2 Protein, Human (Cell-Free, His) Fatty-acid amide hydrolase 2; Amidase domain-containing protein; Anandamide amidohydrolase 2; Oleamide hydrolase 2	Human	E. coli Cell-free
	FAAH2 proteins play a central role in cellular processes by catalyzing the hydrolysis of endogenous amidated lipids, including the sleep-inducing lipid oleamide ((9Z)-octadecylamide) and the endocannabinoid anandamide (N-(5Z) , 8Z, 11Z, 14Z-eicosate tetraenoyl)))-ethanolamine) and other fatty amides. FAAH2 Protein, Human (Cell-Free, His) is the recombinant human-derived FAAH2 protein, expressed by E. coli Cell-free , with N-10*His labeled tag. The total length of FAAH2 Protein, Human (Cell-Free, His) is 532 a.a., with molecular weight of 59.8 kDa.

HY-P71534

	DDX39B Protein, Human (GST) 0610030D10Rik; 4F2-LC6; 56kDa U2AF65-associated protein; AI428441; ATP-dependent RNA helicase p47; B(0,+)-type amino acid transporter 1; BAT1; Bat1a; D17H6S81E; D17H6S81E-1; D6S81E; D6S81Eh; DDX39B; DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B; DEAD box protein UAP56; DX39B_HUMAN; EC 3.6.1.-; Glycoprotein-associated amino acid transporter b0,+AT1; HLA-B-associated transcript 1 protein; HLA-B-associated transcript 1A; HLA-B-associated transcript-1; MGC127051; MGC19235; MGC38799; nuclear RNA helicase (DEAD family); OTTHUMP00000029229; OTTHUMP00000165889; OTTHUMP00000165890; p47; Solute carrier family 7 member 9; Spliceosome RNA helicase BAT1; Spliceosome RNA helicase DDX39B; U2AF65-associayed protein; 56-KD; UAP56	Human	E. coli
	The DDX39B protein intricately coordinates nuclear mRNA export and is specifically associated with spliced mRNA as a key component of the TREX complex. This coupling of mRNA transcription, processing, and export involves rounds of ATP-dependent hydrolysis, recruiting components such as ALYREF/THOC and CHTOP. DDX39B Protein, Human (GST) is the recombinant human-derived DDX39B protein, expressed by E. coli , with N-GST labeled tag. The total length of DDX39B Protein, Human (GST) is 250 a.a., with molecular weight of ~55.2 kDa.

Cat. No.	Product Name		Classification

HY-130923

*BCN-PEG1-Val-Cit-PABC-OH*		ADC Synthesis BCN
BCN-PEG1-Val-Cit-PABC-OH is a cleavable 1 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1]. BCN-PEG1-Val-Cit-PABC-OH is a click chemistry reagent, it contains a BCN group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.

HY-130966

*TCO-PEG1-Val-Cit-PABC-OH*		ADC Synthesis TCO
TCO-PEG1-Val-Cit-PABC-OH is a cleavable 1 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1]. TCO-PEG1-Val-Cit-PABC-OH is a click chemistry reagent, it contains a TCO group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing Tetrazine groups.

HY-136100

*TCO-PEG1-Val-Cit-PABC-PNP*		ADC Synthesis TCO
TCO-PEG1-Val-Cit-PABC-PNP is a cleavable 1 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1]. TCO-PEG1-Val-Cit-PABC-PNP is a click chemistry reagent, it contains a TCO group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing Tetrazine groups.

HY-136105

*Azido-PEG1-Val-Cit-PABC-PNP*		ADC Synthesis Azide
Azido-PEG1-Val-Cit-PABC-PNP is a cleavable 1 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1]. Azido-PEG1-Val-Cit-PABC-PNP is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.

HY-136137

*Azide-PEG1-Val-Cit-PABC-OH*		Azide ADC Synthesis
Azide-PEG1-Val-Cit-PABC-OH is a cleavable 1 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1]. Azide-PEG1-Val-Cit-PABC-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.

HY-140109

*Propargyl-PEG1-SS-PEG1-acid*		Alkynes ADC Synthesis
Propargyl-PEG1-SS-PEG1-acid is a cleavable 2 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1]. Propargyl-PEG1-SS-PEG1-acid is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-140111

*Propargyl-PEG1-SS-PEG1-propargyl*		ADC Synthesis Alkynes
Propargyl-PEG1-SS-PEG1-propargyl is a cleavable 2 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1]. Propargyl-PEG1-SS-PEG1-propargyl is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-140110

*Propargyl-PEG1-SS-PEG1-PFP ester*		Alkynes ADC Synthesis
Propargyl-PEG1-SS-PEG1-PFP ester is a cleavable 1 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1]. Propargyl-PEG1-SS-PEG1-PFP ester is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-130690

*Propargyl-PEG1-SS-PEG1-C2-Boc*		PROTAC Synthesis Alkynes ADC Synthesis
Propargyl-PEG1-SS-PEG1-C2-Boc is a Alkyl/ether-based PROTAC linker can be used in the synthesis of PROTACs. Propargyl-PEG1-SS-PEG1-C2-Boc is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1]. Propargyl-PEG1-SS-PEG1-C2-Boc is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-140280

DBCO-PEG1		DBCO PROTAC Synthesis
DBCO-PEG1 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. DBCO-PEG1 is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.

HY-133138

*Pomalidomide-PEG1-azide*		Azide
Pomalidomide-PEG1-azide is a E3 ligase lgand-linker conjugate. Pomalidomide-PEG1-azide incorporates the Pomalidomide based cereblon ligand and a linker.?Pomalidomide-PEG1-azide?can be used to design a?PROTAC BRD4 Degrader-1 (HY-133131) ^[1]. Pomalidomide-PEG1-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.

HY-133139

*Lenalidomide-PEG1-azide*		Azide
Lenalidomide-PEG1-azide is a E3 ligase lgand-linker conjugate. Lenalidomide-PEG1-azide incorporates the Lenalidomide based cereblon ligand and a linker.?Lenalidomide-PEG1-azide?can be used to design a PROTAC BRD4 Degrader-2 (HY-133136) ^[1]. Lenalidomide-PEG1-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.

HY-161133

*Lenalidomide 4'-PEG1-azide*		Azide
Lenalidomide 4'-PEG1-azide (Compound 4g) is a lenalidomide-derived azide. Lenalidomide 4'-PEG1-azide incorporates the Lenalidomide based cereblon ligand and a linker. Lenalidomide 4'-PEG1-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups. ^[1].

HY-140265

*DBCO-PEG1-acid*		DBCO PROTAC Synthesis
DBCO-PEG1-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. DBCO-PEG1-acid is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.

HY-140038

Bis-propargyl-PEG1		PROTAC Synthesis Alkynes
Bis-propargyl-PEG1 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. Bis-propargyl-PEG1 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-140281

DBCO-C-PEG1		DBCO PROTAC Synthesis
DBCO-C-PEG1 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. DBCO-C-PEG1 is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.

HY-140032

*Alkyne-ethyl-PEG1-Boc* Alkyne-ethyl-PEG1-t-butyl ester		PROTAC Synthesis Alkynes
Alkyne-ethyl-PEG1-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. Alkyne-ethyl-PEG1-Boc is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-140056

*Aminooxy-PEG1-propargyl*		PROTAC Synthesis Alkynes
Aminooxy-PEG1-propargyl is a PEG-based PROTAC linker can be used in the synthesis of PROTACs ^[1]. Aminooxy-PEG1-propargyl is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-140064

*Propargyl-PEG1-acrylate*		PROTAC Synthesis Alkynes
Propargyl-PEG1-acrylate is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. Propargyl-PEG1-acrylate is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-140271

*DBCO-PEG1-NHS ester*		DBCO PROTAC Synthesis
DBCO-PEG1-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. DBCO-PEG1-NHS ester is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.

HY-140282

*DBCO-PEG1-amine*		DBCO PROTAC Synthesis
DBCO-PEG1-amine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. DBCO-PEG1-amine is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.

HY-138334

*Propargyl-PEG1-THP*		Alkynes PROTAC Synthesis
Propargyl-PEG1-THP is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. Propargyl-PEG1-THP is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-W096146

*Propynyl-PEG1-Ac*		Alkynes PROTAC Synthesis
Propynyl-PEG1-Ac is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. Propynyl-PEG1-Ac is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-126513

*Propargyl-PEG1-NHS ester*		ADC Synthesis Alkynes
Propargyl-PEG1-NHS ester is a nonclaevable 1-unit PEG linker for antibody-agent-conjugation (ADC). Propargyl-PEG1-NHS ester is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-140026

*Propargyl-PEG1-Boc*		Alkynes PROTAC Synthesis
Propargyl-PEG1-Boc is an alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. Propargyl-PEG1-Boc is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-140049

*Boc-aminooxy-PEG1-propargyl*		PROTAC Synthesis Alkynes
Boc-aminooxy-PEG1-propargyl is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. Boc-aminooxy-PEG1-propargyl is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-140289

*DBCO-PEG1-NH-Boc*		DBCO PROTAC Synthesis
DBCO-PEG1-NH-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. DBCO-PEG1-NH-Boc is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.

HY-133510

*Bis-BCN-PEG1-diamide*		PROTAC Synthesis BCN
Bis-BCN-PEG1-diamide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. Bis-BCN-PEG1-diamide is a click chemistry reagent, it contains a BCN group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.

HY-157514

*Thalidomide 4'-ether-PEG1-azide*		Azide
Thalidomide 4'-ether-PEG1-azide is the Thalidomide (HY-14658)-based cereblon ligand used in the recruitment of CRBN protein. Thalidomide 4'-ether-PEG1-azide can be connected to the ligand for protein by a linker to form PROTACs ^[1].

HY-116069

*Propargyl-PEG1-NH2*		Alkynes PROTAC Synthesis
Propargyl-PEG1-NH2 is a PEG-based PROTAC linker can be used in the synthesis of PROTACs ^[1]. Propargyl-PEG1-NH2 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-140108

*Propargyl-PEG1-SS-alcohol*		Alkynes ADC Synthesis
Propargyl-PEG1-SS-alcohol is a cleavable 1 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1]. Propargyl-PEG1-SS-alcohol is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-138461

Azido-PEG1		Azide PROTAC Synthesis
Azido-PEG1 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs ^[1]. Azido-PEG1 is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.

HY-130922

*BCN-PEG1-Val-Cit-OH*		BCN ADC Synthesis
BCN-PEG1-Val-Cit-OH is a cleavable 1 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1]. BCN-PEG1-Val-Cit-OH is a click chemistry reagent, it contains a BCN group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.

HY-130934

*TCO-PEG1-Val-Cit-OH*		TCO ADC Synthesis
TCO-PEG1-Val-Cit-OH is a cleavable 1 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) ^[1]. TCO-PEG1-Val-Cit-OH is a click chemistry reagent, it contains a TCO group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing Tetrazine groups.

HY-126948

*Aminooxy-PEG1-azide*		Azide PROTAC Synthesis
Aminooxy-PEG1-azide is a PEG-based PROTAC linker can be used in the synthesis of PROTACs ^[1]. Aminooxy-PEG1-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.

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MC-(β-Ala)-PABC-(β-D-GlcUA)-amide-PEG1-CH2-CC-885

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