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Results for "

2-2-6-dioxopiperidin-3-yl-phthalimidine-piperazine-c-piperidine-hydro

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Adenosine Receptor (1) Amino Acid Derivatives (1) Apolipoprotein (1) Apoptosis (8) Autophagy (8) Bacterial (1) Bcl-2 Family (1) Biochemical Assay Reagents (5) Btk (1) Drug Derivative (7) Drug Intermediate (4) E3 Ligase Ligand-Linker Conjugates (36) Ferroptosis (2) GABA Receptor (1) Isotope-Labeled Compounds (8) LDLR (1) Ligands for E3 Ligase (12) Ligands for Target Protein for PROTAC (2) Melanocortin Receptor (1) MOFs (1) Parasite (1) Phosphodiesterase (PDE) (1) PROTAC Linkers (11) PROTACs (1) Protein Arginine Deiminase (1) Reference Standards (5) Target Protein Ligand-Linker Conjugates (3) TNF Receptor (2)
By Research Areas:	Cancer (67) Cardiovascular Disease (1) Infection (2) Inflammation/Immunology (1) Metabolic Disease (1) Neurological Disease (11)

By Targets:

Adenosine Receptor (1)

Amino Acid Derivatives (1)

Apolipoprotein (1)

Apoptosis (8)

Autophagy (8)

Bacterial (1)

Bcl-2 Family (1)

Biochemical Assay Reagents (5)

Btk (1)

Drug Derivative (7)

Drug Intermediate (4)

E3 Ligase Ligand-Linker Conjugates (36)

Ferroptosis (2)

GABA Receptor (1)

Isotope-Labeled Compounds (8)

LDLR (1)

Ligands for E3 Ligase (12)

Ligands for Target Protein for PROTAC (2)

Melanocortin Receptor (1)

MOFs (1)

Parasite (1)

Phosphodiesterase (PDE) (1)

PROTAC Linkers (11)

PROTACs (1)

Protein Arginine Deiminase (1)

Reference Standards (5)

Target Protein Ligand-Linker Conjugates (3)

TNF Receptor (2)

By Research Areas:

Cancer (67)

Cardiovascular Disease (1)

Infection (2)

Inflammation/Immunology (1)

Metabolic Disease (1)

Neurological Disease (11)

100

Inhibitors & Agonists

Biochemical Assay Reagents

Peptides

Natural
Products

Protéines recombinantes

Isotope-Labeled Compounds

Antibodies

Cat. No.	Nom du produit	Target	Áreas de investigación	Chemical Structure

HY-44432

Navitoclax-piperazine ABT-263-piperazine	Ligands for Target Protein for PROTAC Bcl-2 Family	Cancer
Navitoclax-piperazine (ABT-263-piperazine) is a Navitoclax (HY-10087) analog and BCL-XL inhibitor. Navitoclax-piperazine is the ligand for target protein of PROTAC DT2216 (HY-130604). Navitodax-pperaie and E3 ubiquitin ligase VHL ligand can be used to synthesize PROTAC DT2216 (HY-130604) .

HY-W002603

*Benzyl piperazine-1-carboxylate*	Biochemical Assay Reagents Drug Intermediate	Neurological Disease
Benzyl piperazine-1-carboxylate is a synthetic intermediate that can be used in the research of melanocortin-4 (MC4) receptor antagonists .

HY-P2336A

CCZ01048 TFA 3 Publications Verification	Melanocortin Receptor	Cancer
CCZ01048 TFA, a α-MSH analogue, exhibits high binding affinity to melanocortin 1 receptor (MC1R) with a K_i of 0.31 nM. CCZ01048 TFA shows rapid internalization into B16F10 melanoma cells and high in vivo stability. CCZ01048 TFA is a promising candidate for PET imaging of malignant melanoma .

HY-139116

Piperidine-4-sulfonic acid 1 Publications Verification	GABA Receptor	Neurological Disease
Piperidine-4-sulfonic acid is a potent GABA agonist with an IC₅₀ of 0.034 μM for the inhibition of the binding of H-GABA .

HY-W259932

*Lenalidomide 5'-piperazine* hydrochloride**	Ligands for E3 Ligase	Cancer
Lenalidomide 5'-piperazine hydrochloride can serve as a Cereblon ligand to recruit CRBN protein. Lenalidomide 5'-piperazine hydrochloride can be linked to target protein ligands via a linker to form PROTAC molecules, such as KI-CDK9d-32 (HY-173523) .

HY-100887

Piperazine Erastin Maximum Cited Publications 9 Publications Verification	Ferroptosis	Cancer
Piperazine erastin is an analog of erastin which induces an iron-dependent form of non-apoptotic cell death, termed ferroptosis. Piperazine erastin can be used in cancer research .

HY-W011726

*1-(4-Methoxyphenyl)piperazine* hydrochloride** piperazine, 1- (4-methoxyphenyl)-, dihydrochloride	Drug Derivative	Neurological Disease
1-(4-Methoxyphenyl)piperazine (Piperazine, 1- (4-methoxyphenyl)-) hydrochloride is a piperazine derivative with neural activity .

HY-W045082

*tert-Butyl 4-(piperidine-4-carbonyl)piperazine-1-carboxylate*	PROTAC Linkers	Cancer
tert-Butyl 4-(piperidine-4-carbonyl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.

HY-131386A

*BMS-1166-N-piperidine-CO-N-piperazine* dihydrochloride**	Target Protein Ligand-Linker Conjugates	Cancer
BMS-1166-N-piperidine-CO-N-piperazine dihydrochloride incorporates a ligand for PD-1/PD-L1 immune checkpoint, and a PROTAC linker. BMS-1166-N-piperidine-CO-N-piperazine dihydrochloride can be used in the synthesis of PROTAC PD-1/PD-L1 degrader-1?(HY-131183). PROTAC PD-1/PD-L1 degrader-1 inhibits PD-1/PD-L1 interaction with an IC₅₀ of 39.2 nM .

HY-157566

*Lenalidomide 5'-piperazine-4-methylpiperidine hydrochloride*	Ligands for E3 Ligase	Cancer
Lenalidomide 5'-piperazine-4-methylpiperidine hydrochloride is a functionalized cerebellar ligand for PROTAC development, combining E3 ligand and terminal piperidine for subsequent chemical reactions. A protein degradant with a rigid connector is generated .

HY-40041

(R)-1-Boc-3-methyl-piperazine	Biochemical Assay Reagents Drug Intermediate	Cancer
(R)-1-Boc-3-methyl-piperazine (Compound I3-1) is a chemical intermediate. (R)-1-Boc-3-methyl-piperazine can be used for the preparation of Compound I3. Compound I3 exhibits anticancer activity against colorectal adenocarcinoma with BRCA2 gene deletion .

HY-160244

*Pomalidomide 5'-piperazine-4-methylpiperidine dihydrochloride*	Ligands for E3 Ligase	Cancer
Pomalidomide 5'-piperazine-4-methylpiperidine dihydrochloride is the Pomalidomide (HY-10984)-based cereblon (CRBN) ligand used in the recruitment of CRBN protein. Pomalidomide 5'-piperazine-4-methylpiperidine dihydrochloride can be connected to the ligand for protein by a linker to form PROTAC.

HY-400601

*tert-Butyl (2-(2-chloro-4-(3-((2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolin-5-yl)methyl)ureido)phenethoxy)ethyl)(methyl)carbamate*	Drug Intermediate	Others
tert-Butyl (2-(2-chloro-4-(3-((2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolin-5-yl)methyl)ureido)phenethoxy)ethyl)(methyl)carbamate is a drug intermediate for synthesis of various active compounds.

HY-138783A

*Thalidomide-Piperazine-Piperidine* hydrochloride**	E3 Ligase Ligand-Linker Conjugates	Cancer
Thalidomide-Piperazine-Piperidine hydrochloride is a synthesized E3 ligase ligand-linker conjugate. Thalidomide-Piperazine-Piperidine hydrochloride incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology .

HY-W008813

1-(3-Methoxyphenyl)piperazine	Biochemical Assay Reagents	Others
1-(3-Methoxyphenyl)piperazine (Compound 4) is an analytical reference standard categorized as a piperazine .

HY-138793

2-(2,6-Dioxopiperidin-3-yl)phthalimidine 1 Publications Verification EM-12	TNF Receptor Ligands for E3 Ligase	Cancer
2-(2,6-Dioxopiperidin-3-yl)phthalimidine (EM-12), a teratogenic Thalidomide analogue, is more active than Thalidomide and is much more stable for hydrolysis. 2-(2,6-Dioxopiperidin-3-yl)phthalimidine enhances 1,2-dimethylhydrazine-induction of rat colon adenocarcinomas .

HY-B1505A

Acefylline piperazine Theophyllineacetic acid piperazine; Theophylline-7-acetic acid piperazine	Adenosine Receptor Protein Arginine Deiminase Phosphodiesterase (PDE)	Cardiovascular Disease Neurological Disease Inflammation/Immunology
Acefylline (Theophyllineacetic acid) piperazine, a xanthine derivative, is an Adenosine Receptor antagonist. Acefylline piperazine is a peptidylarginine deiminase (PAD) activator. Acefylline piperazine is also a bronchodilator and cardiac stimulant that inhibits rat lung cAMP phosphodiesterase isoenzymes. Acefylline piperazine can be used in asthma research .

HY-130983

*N-piperidine* Ibrutinib hydrochloride**	Btk Ligands for Target Protein for PROTAC	Cancer
N-piperidine Ibrutinib hydrochloride (Compound 1) is a reversible Ibrutinib derivative. N-piperidine Ibrutinib hydrochloride is a potent BTK inhibitor with IC₅₀s of 51.0 and 30.7 nM for WT BTK and C481S BTK, respectively . N-piperidine Ibrutinib hydrochloride can be used as a BTK ligand in the synthesis of a series of PROTACs, such as SJF620 (HY-133137). SJF620 is a potent PROTAC BTK degrader with a DC₅₀ of 7.9 nM .

HY-W1115215B

*2-(2,6-Dioxopiperidin-3-yl)phthalimidine-Piperazine-piperidine* dihydrochloride**	E3 Ligase Ligand-Linker Conjugates	Cancer
2-(2,6-Dioxopiperidin-3-yl)phthalimidine-Piperazine-piperidine dihydrochloride is an E3 ligase ligand-linker conjugate containing a CRBN-based ligand and linker, which can be used to synthesize PROTAC.

HY-W457960

*2-(2,6-Dioxopiperidin-3-yl)-5-ethynylisoindoline-1,3-dione*	Ligands for E3 Ligase	Cancer
2-(2,6-Dioxopiperidin-3-yl)-5-ethynylisoindoline-1,3-dione is a Thalidomide analog that can be useful in PROTAC research.

HY-W584986

Thalidomide-(2)piperidine	Ligands for E3 Ligase	Cancer
Thalidomide-(2)piperidine (compound 9) is a potent E3 ligase ligand. Thalidomide-(2)piperidine can be used for synthesis of PROTACs .

HY-33540S

*1-(Chlorocarbonyl)piperidine-d10*	Isotope-Labeled Compounds	Others
1-(Chlorocarbonyl)piperidine-d₁₀ is the deuterium labeled 1-(Chlorocarbonyl)piperidine .

HY-W797383

Phthalimidinoglutarimide-6-piperazine	E3 Ligase Ligand-Linker Conjugates	Cancer
Phthalimidinoglutarimide-6-piperazine is a conjugate of E3 ubiquitin ligase ligand-Linker, which can be used to synthesize complete PROTACs molecules.

HY-78871S

1-(Methyl-d3)piperazine	Isotope-Labeled Compounds	Others
1-(Methyl-d₃)piperazine is the deuterium labeled N-Methylpiperazine .

HY-132971

*Thalidomide-piperazine* hydrochloride**	Ligands for E3 Ligase Apoptosis Autophagy	Cancer
Thalidomide-piperazine hydrochloride is a synthetic E3 ligase ligand-linker conjugate, comprising a cereblon ligand based on Thalidomide (HY-14658) and one linker. Thalidomide-piperazine hydrochloride can be used in studies related to PROTAC synthesis .

HY-138783

Thalidomide-Piperazine-Piperidine	E3 Ligase Ligand-Linker Conjugates Autophagy Apoptosis	Cancer
Thalidomide-Piperazine-Piperidine is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology .

HY-W1115542

2-(2,6-Dioxopiperidin-3-yl)phthalimidine-1-(piperidin-4-ylmethyl)piperidine	E3 Ligase Ligand-Linker Conjugates	Cancer
2-(2,6-Dioxopiperidin-3-yl)phthalimidine-1-(piperidin-4-ylmethyl)piperidine is an E3 ligase ligand-linker conjugate containing a CRBN-based ligand and linker, which can be used to synthesize PROTAC.

HY-W1115204

*Lenalidomide 5'-piperazine-C1-piperidine* hydrochloride**	E3 Ligase Ligand-Linker Conjugates	Cancer
Lenalidomide 5'-piperazine-C1-piperidine hydrochloride is an E3 ligase ligand-linker conjugate containing a CRBN-based ligand and linker, which can be used to synthesize PROTAC.

HY-W1115215

2-(2,6-Dioxopiperidin-3-yl)phthalimidine-Piperazine-piperidine	E3 Ligase Ligand-Linker Conjugates	Cancer
2-(2,6-Dioxopiperidin-3-yl)phthalimidine-Piperazine-piperidine is an E3 ligase ligand-linker conjugate containing a CRBN-based ligand and linker, which can be used to synthesize PROTAC.

HY-W1115215A

*2-(2,6-Dioxopiperidin-3-yl)phthalimidine-Piperazine-piperidine* hydrochloride**	E3 Ligase Ligand-Linker Conjugates	Cancer
2-(2,6-Dioxopiperidin-3-yl)phthalimidine-Piperazine-piperidine hydrochloride is an E3 ligase ligand-linker conjugate containing a CRBN-based ligand and linker, which can be used to synthesize PROTAC.

HY-W1115219

*2-(2,6-Dioxopiperidin-3-yl)phthalimidine-piperazine-C-piperidine* hydrochloride**	E3 Ligase Ligand-Linker Conjugates	Cancer
2-(2,6-Dioxopiperidin-3-yl)phthalimidine-piperazine-C-piperidine hydrochloride is an E3 ligase ligand-linker conjugate containing a CRBN-based ligand and linker, which can be used to synthesize PROTAC.

HY-132939

*2-(2,6-Dioxopiperidin-3-yl)phthalimidine-C5-Br*	E3 Ligase Ligand-Linker Conjugates	Cancer
2-(2,6-Dioxopiperidin-3-yl)phthalimidine-C5-Br is a E3 ligase ligand-linker conjugate for PROTAC.

HY-W012748S

Piperidine-4-carboxamide-d9	Isotope-Labeled Compounds	Others
Piperidine-4-carboxamide-d₉ is the deuterium labeled Piperidine-4-carboxamide .

HY-178512

**Piperazine-CO-C1-Azacyclohexane-C1-Piperazine**	PROTAC Linkers	Cancer
Piperazine-CO-C1-Azacyclohexane-C1-Piperazine is a PROTAC linker can be used in the synthesis of PROTACs, such as PROTAC CDK4/6/9 degrader 1 (HY-178452) .

HY-W874585

2-(2,6-Dioxopiperidin-3-yl)phthalimidine-piperidine	E3 Ligase Ligand-Linker Conjugates	Cancer
2-(2,6-Dioxopiperidin-3-yl)phthalimidine-piperidine is an E3 ligase ligand-linker conjugate containing a CRBN-based ligand and linker, which can be used to synthesize PROTAC.

HY-176187

DDR1 ligand 1-piperidine	Target Protein Ligand-Linker Conjugates	Cancer
DDR1 ligand 1-piperidine is a target protein ligand and linker conjugate, which can be used for the synthesis of PROTAC DDR1 degrader-1 (HY-176184) .

HY-W1114860

2-(2,6-Dioxopiperidin-3-yl)phthalimidine-alkyne-piperidine	E3 Ligase Ligand-Linker Conjugates	Cancer
2-(2,6-Dioxopiperidin-3-yl)phthalimidine-alkyne-piperidine is an E3 ligase ligand-linker conjugate containing a CRBN-based ligand and linker, which can be used to synthesize PROTAC.

HY-W1112836

2-(2,6-Dioxopiperidin-3-yl)phthalimidine-O-piperidine	E3 Ligase Ligand-Linker Conjugates	Cancer
2-(2,6-Dioxopiperidin-3-yl)phthalimidine-O-piperidine is an E3 ligase ligand-linker conjugate containing a CRBN-based ligand and linker, which can be used to synthesize PROTAC.

HY-159017

*2-(2,6-Dioxopiperidin-3-yl)phthalimidine* NMe-alkyne-C6-OMs**	E3 Ligase Ligand-Linker Conjugates	Cancer
EM-12-Alkyne-C6-OMs is a conjugate of E3 ligase ligand and linker, consisting of 2-(2,6-Dioxopiperidin-3-yl)phthalimidine (EM-12) (HY-138793) and the corresponding Linker (HY-159018). EM-12-Alkyne-C6-OMs can be used to synthesize PROTACs .

HY-W904851

*Boc-Piperidine-piperazine-Cbz*	PROTAC Linkers	Cancer
Boc-Piperidine-piperazine-Cbz is a PROTAC linker that can be used in the synthesis of ZLC491 (HY-168162) .

HY-168217

*Thalidomide-piperazine-piperidine-2-F-Ph-CHO*	E3 Ligase Ligand-Linker Conjugates	Cancer
Thalidomide-piperazine-piperidine-2-F-Ph-CHO is a E3 ligase ligand-linker conjugate, which is consisted of a Thalidomide (HY-14658) and a linker Boc-Piperazine-piperidine-2-F-Ph-CHO (HY-168218). Thalidomide-piperazine-piperidine-2-F-Ph-CHO is utilized for synthesis of PROTAC molecule YDR1 (HY-168215) .

HY-168388

Piperidine-C2-piperazine-Boc	PROTAC Linkers	Cancer
Piperidine-C2-piperazine-Boc is a PROTAC linker that can be used in the synthesis of PROTACs .

HY-168389

*Thalidomide-piperidine-C2-piperazine-Boc*	E3 Ligase Ligand-Linker Conjugates	Cancer
Thalidomide-piperidine-C2-piperazine-Boc is an E3 ligase ligand-linker conjugate that incorporates the Thalidomide (HY-130639) based cereblon ligand and a linker used in PROTAC technology. Thalidomide-piperidine-C2-piperazine-Boc can be used for synthesis of PROTACs .

HY-W1003884

Lenalidomide 5'-piperazine-C1-piperidine	E3 Ligase Ligand-Linker Conjugates	Cancer
Lenalidomide 5'-piperazine-C1-piperidine is an E3 ligase ligand-linker conjugate containing a CRBN-based ligand and linker, which can be used to synthesize PROTAC.

HY-161195

*Deoxy-thalidomide-piperidine-C-piperazine-C-boc*	E3 Ligase Ligand-Linker Conjugates Autophagy Apoptosis	Cancer
Deoxy-thalidomide-piperidine-C-piperazine-C-boc is a conjugate of E3 ligase ligand and linker, consisting of Thalidomide (HY-14658) and the corresponding Linker. Deoxy-thalidomide-piperidine-C-piperazine-C-boc can serve as a Cereblon ligand to recruit CRBN protein and serve as a key intermediate for the synthesis of complete PROTAC molecules.

HY-W1115226

*Desamino lenalidomide-piperidine-C-piperazine* hydrochloride**	E3 Ligase Ligand-Linker Conjugates	Cancer
Desamino lenalidomide-piperidine-C-piperazine hydrochloride is an E3 ligase ligand-linker conjugate containing a CRBN-based ligand and linker, which can be used to synthesize PROTAC.

HY-168197

*Thalidomide-F-piperidine-piperazine-Cbz*	PROTACs	Cancer
Thalidomide-F-piperidine-piperazine-Cbz Conjugate 110 is a conjugate of E3 ligase and linker for the synthesis of CDK12/13 PROTAC degrader (HY-168162) .

HY-161184

*Deoxy-thalidomide-piperidine-C-piperazine-C2-OH*	E3 Ligase Ligand-Linker Conjugates Autophagy Apoptosis	Cancer
Deoxy-thalidomide-piperidine-C-piperazine-C2-OH is a conjugate of E3 ligase ligand and linker, consisting of Thalidomide (HY-14658) and the corresponding Linker. Deoxy-thalidomide-piperidine-C-piperazine-C2-OH can serve as a Cereblon ligand to recruit CRBN protein and serve as a key intermediate for the synthesis of complete PROTAC molecules.

HY-168218

*Boc-Piperazine-piperidine-2-F-Ph-CHO*	PROTAC Linkers	Cancer
Boc-Piperazine-piperidine-2-F-Ph-CHO is a PROTAC linker that can be used in the synthesis of YDR1 (HY-168215) .

HY-131386

BMS-1166-N-piperidine-CO-N-piperazine	Target Protein Ligand-Linker Conjugates	Cancer
BMS-1166-N-piperidine-CO-N-piperazine incorporates a ligand for PD-1/PD-L1 immune checkpoint, and a PROTAC linker. BMS-1166-N-piperidine-CO-N-piperazine can be used in the synthesis of PROTAC PD-1/PD-L1 degrader-1?(HY-131183). PROTAC PD-1/PD-L1 degrader-1 inhibits PD-1/PD-L1 interaction with an IC₅₀ of 39.2 nM .

Cat. No.	Nom du produit	Type

HY-W002603

*Benzyl piperazine-1-carboxylate*	Biochemical Assay Reagents
Benzyl piperazine-1-carboxylate is a synthetic intermediate that can be used in the research of melanocortin-4 (MC4) receptor antagonists .

HY-40041

(R)-1-Boc-3-methyl-piperazine	Biochemical Assay Reagents
(R)-1-Boc-3-methyl-piperazine (Compound I3-1) is a chemical intermediate. (R)-1-Boc-3-methyl-piperazine can be used for the preparation of Compound I3. Compound I3 exhibits anticancer activity against colorectal adenocarcinoma with BRCA2 gene deletion .

Cat. No.	Nom du produit	Target	Research Area

HY-P2336A

CCZ01048 TFA 3 Publications Verification	Melanocortin Receptor	Cancer
CCZ01048 TFA, a α-MSH analogue, exhibits high binding affinity to melanocortin 1 receptor (MC1R) with a K_i of 0.31 nM. CCZ01048 TFA shows rapid internalization into B16F10 melanoma cells and high in vivo stability. CCZ01048 TFA is a promising candidate for PET imaging of malignant melanoma .

Cat. No.	Nom du produit	Category	Target	Chemical Structure

HY-W438378

4-Hydroxy-3-methoxyphenylglycol piperazine HMPG piperazine	Monophenols Phenols Endogenous metabolite Source Classification	Biochemical Assay Reagents
4-Hydroxy-3-methoxyphenylglycol piperazine (HMPG piperazine) is a salt of HMPG combined with piperazine. HMPG is a metabolite of adrenaline and norepinephrine and is an important marker of catecholamine hormone metabolism in the body. 4-Hydroxy-3-methoxyphenylglycol piperazine is used as a standard in clinical laboratories to accurately measure the HMPG content in urine .

Species:	Human (3) Mouse (3)
Tag:	His (6)
Source:	P. pastoris (1) E. coli (5)

Cat. No.	Compare	Nom du produit	Species	Source	Image

HY-P705495

	Gamma-enolase/Enolase 2 Protein, Mouse (His) phosphopyruvate hydratase; Eno2; 2-phospho-D-glycerate hydro-lyase	Mouse	E. coli

HY-P705529

	ENO3 Protein, Mouse (P. pastoris, His) Beta-enolase; 2-phospho-D-glycerate hydro-lyase; Enolase 3; Muscle-specific enolase (MSE); Skeletal muscle enolase	Mouse	P. pastoris

HY-P72182

	Enolase 1/ENO1 Protein, Mouse (His) Eno1; Eno-1; Alpha-enolase; EC 4.2.1.11; 2-phospho-D-glycerate hydro-lyase; Enolase 1; Non-neural enolase; NNE	Mouse	E. coli
	Enolase 1/ENO1 Proteins, as a glycolytic enzyme, convert 2-phosphoglycerate to phosphoenolpyruvate and have diverse roles in cellular processes like growth control, hypoxia tolerance, and allergic responses. They also function in the fibrinolytic system and stimulate immunoglobulin production, showing their involvement in immune responses. Enolase 1/ENO1 Protein, Mouse (His) is the recombinant mouse-derived Enolase 1/ENO1 protein, expressed by E. coli , with N-10*His labeled tag.

HY-P70271

	Gamma-enolase/Enolase 2 Protein, Human (His) rHuGamma-enolase/ENO2, His; Gamma-enolase; 2-phospho-D-glycerate hydro-lyase; Enolase 2; Neural enolase; Neuron-specific enolase; NSE; ENO2	Human	E. coli
	Gamma-enolase/Enolase 2 protein exhibits neurotrophic and neuroprotective properties, binding to neocortical neurons and promoting cell survival through a calcium-dependent mechanism. This suggests its potential role in supporting neuron viability within the central nervous system. Gamma-enolase/Enolase 2 Protein, Human (His) is the recombinant human-derived Gamma-enolase/Enolase 2 protein, expressed by E. coli , with N-6*His labeled tag.

HY-P70260A

	Enolase 1/ENO1 Protein, Human (His) rHuAlpha-enolase, His; Alpha-enolase; 2-phospho-D-glycerate hydro-lyase; C-myc promoter-binding protein; Enolase 1; MBP-1; MPB-1; Non-neural enolase; NNE; Phosphopyruvate hydratase; Plasminogen-binding protein; ENO1	Human	E. coli
	The ENO1 protein converts 2-phosphoglycerate to phosphoenolpyruvate and is involved in growth control, hypoxia tolerance, and allergic responses. It acts as a receptor and activator of plasminogen, stimulating immunoglobulin production. ENO1 binds to the myc promoter as a transcriptional repressor and may function as a tumor suppressor. Enolase 1/ENO1 Protein, Human (His) is the recombinant human-derived Enolase 1/ENO1 protein, expressed by E. coli , with C-6*His labeled tag.

HY-P70260

	Enolase 1/ENO1 Protein, Human (His, solution) rHuAlpha-enolase, His; Alpha-enolase; 2-phospho-D-glycerate hydro-lyase; C-myc promoter-binding protein; Enolase 1; MBP-1; MPB-1; Non-neural enolase; NNE; Phosphopyruvate hydratase; Plasminogen-binding protein; ENO1	Human	E. coli
	The ENO1 protein converts 2-phosphoglycerate to phosphoenolpyruvate and is involved in growth control, hypoxia tolerance, and allergic responses. It acts as a receptor and activator of plasminogen, stimulating immunoglobulin production. ENO1 binds to the myc promoter as a transcriptional repressor and may function as a tumor suppressor. Enolase 1/ENO1 Protein, Human (His, solution) is the recombinant human-derived ENO1, expressed by E. coli , with C-His labeled tag.

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Cat. No.	Nom du produit	Chemical Structure

HY-33540S

*1-(Chlorocarbonyl)piperidine-d10*
1-(Chlorocarbonyl)piperidine-d₁₀ is the deuterium labeled 1-(Chlorocarbonyl)piperidine .

HY-78871S

1-(Methyl-d3)piperazine
1-(Methyl-d₃)piperazine is the deuterium labeled N-Methylpiperazine .

HY-W012748S

Piperidine-4-carboxamide-d9
Piperidine-4-carboxamide-d₉ is the deuterium labeled Piperidine-4-carboxamide .

HY-W707900

*Erythro-hydro* bupropion-d9 (enantiomer)hydrochloride**
Erythro-hydro bupropion-d₉ (enantiomer)(hydrochloride) is deuterium labeled (1R,2S)-2-(Tert-butylamino)-1-(3-chlorophenyl)propan-1-ol hydrochloride .

HY-W768527

*Methyl piperidine-4-carboxylate hydrochloride-13C3*
Methyl piperidine-4-carboxylate hydrochloride- ¹³C₃ is the ¹³C-labeled Methyl piperidine-4-carboxylate hydrochloride (HY-W002947).

HY-W578976S

*N-Boc-piperazine-d4*
N-Boc-piperazine-d₄ is the deuterium labeled N-Boc-piperazine.

HY-W701440

Piperazine-d8 TFA
Piperazine-d₈ TFA is the deuterium labeled Piperazine trifluoroacetate.

HY-139508S

*4-Benzhydryloxy-piperidine-d5*
4-(Diphenylmethoxy)piperidine-d₅ is the deuterium labeled 4-(Diphenylmethoxy)piperidine .

Host:	Mouse (4) Rabbit (3)
Reactivity:	Human (7) Rat (7) Mouse (7)
Application:	IHC-P (3) ICC/IF (4) IP (1) IHC-F (1) WB (7) ELISA (3)
Isotype:	IgG (3) IgG1 (4)
Conjugation:	Non-conjugated (7)
Clonality:	Monoclonal (5) Recombinant (2)
Modification:	Unmodified (5)

Cat. No.	Compare	Nom du produit	Application	Reactivity	Image

HY-P82406

	Aconitase 2 Antibody (YA2151) Aconitate hydratase; mitochondrial; Aconitase; Citrate hydro-lyase	WB, IHC-P, ICC/IF, IP	Human, Mouse, Rat
	Aconitase 2 Antibody (YA2151) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to Aconitase 2.

HY-P81290

	NSE Antibody (YA1004) ENO2; Gamma-enolase; 2-phospho-D-glycerate hydro-lyase; Enolase 2; Neural enolase; Neuron-specific enolase; NSE	WB, ELISA	Human, Mouse, Rat
	NSE Antibody (YA1004) is a Mouse-derived and non-conjugated IgG1 monoclonal antibody, targeting to NSE.

HY-P81290B

	NSE Antibody (YA1006) ENO2; Gamma-enolase; 2-phospho-D-glycerate hydro-lyase; Enolase 2; Neural enolase; Neuron-specific enolase; NSE	WB, IHC-F, IHC-P, ICC/IF	Human, Mouse, Rat
	NSE Antibody (YA1006) is a Mouse-derived and non-conjugated IgG1 monoclonal antibody, targeting to NSE.

HY-P81290A

	NSE Antibody (YA1005) ENO2; Gamma-enolase; 2-phospho-D-glycerate hydro-lyase; Enolase 2; Neural enolase; Neuron-specific enolase; NSE	WB, ELISA	Human, Mouse, Rat
	NSE Antibody (YA1005) is a Mouse-derived and non-conjugated IgG1 monoclonal antibody, targeting to NSE.

HY-P81290AA

	NSE Antibody (YA1005)(PBS only) ENO2; Gamma-enolase; 2-phospho-D-glycerate hydro-lyase; Enolase 2; Neural enolase; Neuron-specific enolase; NSE	WB, ELISA	Human, Mouse, Rat
	NSE Antibody (YA1005) is a Mouse-derived and non-conjugated IgG1 monoclonal antibody, targeting to NSE.

HY-P811169

	Phospho-Aconitase 1 (Ser138) Antibody IREB1, ACO1, Cytoplasmic aconitate hydratase, Aconitase, Citrate hydro-lyase, Ferritin repressor protein, Iron regulatory protein 1, Iron-responsive element-binding protein 1, IRP1, IRE-BP 1	WB, IHC-P, ICC/IF	Human, Mouse, Rat
	Phospho-Aconitase 1 (Ser138) Antibody is a Rabbit-derived and non-conjugated IgG Polyclonal antibody, targeting to Phospho-Aconitase 1 (Ser138).

HY-P83105

	Aconitase 1 Antibody (YA2850) ACO1; IREB1; Cytoplasmic aconitate hydratase; Aconitase; Citrate hydro-lyase; Ferritin repressor protein; Iron regulatory protein 1; IRP1; Iron-responsive element-binding protein 1; IRE-BP 1	WB, ICC/IF	Human, Mouse, Rat
	Aconitase 1 Antibody (YA2850) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to Aconitase 1.