67 Results for "

Val-Ala

" in MedChemExpress (MCE) Product Catalog:
Products (67)

67 Results for "Val-Ala" in MCE Product Catalog:

207
207 Publications Verification
Cat. No.: HY-16658
CAS No.: 187389-52-2
Synonyms: Z-Val-Ala-Asp(OMe)-FMK
Target:  

Caspase

Research Areas:  

Cancer

Z-VAD(OMe)-FMK (Z-Val-Ala-Asp(OMe)-FMK) is a cell-permeable and irreversible pan-caspase inhibitor . Z-VAD(OMe)-FMK is an ubiquitin carboxy-terminal hydrolase L1 (UCHL1) inhibitor. Z-VAD(OMe)-FMK irreversibly modifies UCHL1 by targeting the active site of UCHL1 .
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1 Cited Publications
Cat. No.: HY-147095
CAS No.: 2845164-91-0
Purity:  99.90%
Research Areas:  

Cancer

Val-Ala-PABC-Exatecan is a Drug-Linker Conjugates for ADC, consiting of a cleavable Tesirine linker (Val-Ala-PABC) and Exatecan (HY-13631) (topoisomerase I inhibitor). Val-Ala-PABC-Exatecan can be used for ADC molecues synthesis, such as Mal-PEGn-amide-va-Exatecan .
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1 Cited Publications
Cat. No.: HY-W007035
CAS No.: 27493-61-4
Synonyms: Valyl-Alanine
H-Val-Ala-OH (Valyl-alanine) is a dipeptide formed from L-Valine and L-Alanine residues. H-Val-Ala-OH has a role as a metabolite and also has a bitter taste .
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1 Cited Publications
Cat. No.: HY-101153
CAS No.: 1342211-31-7
Purity:  99.79%
Target:  

ADC Linkers

Research Areas:  

Cancer

MC-Val-Ala-OH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
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1 Cited Publications
Cat. No.: HY-P4322
CAS No.: 131167-89-0
Target:  

ERK Akt

Research Areas:  

Neurological Disease Cancer

H-Ile-Lys-Val-Ala-Val-OH is one of the most potent active sites of laminin-1. H-Ile-Lys-Val-Ala-Val-OH promotes cell adhesion, neurite outgrowth, and tumor growth. H-Ile-Lys-Val-Ala-Val-OH stimulates BMMSC population growth and proliferation by activating MAPK/ERK1/2 and PI3K/Akt signalling pathways .
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1 Cited Publications
Cat. No.: HY-147095A
CAS No.: 2928571-45-1
Purity:  98.39%
Research Areas:  

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 .
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Cat. No.: HY-148820
CAS No.: 2857037-70-6
Purity:  98.65%
Research Areas:  

Cancer

Br-Val-Ala-NH2-bicyclo[1.1.1]pentane-7-MAD-MDCPT (Formula V) is a agent-linker conjugate that composed of a potent topoisomerase I inhibitor and a linker to make an antibody agent conjugate (ADC), ABBV-969 .
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Cat. No.: HY-126364
CAS No.: 1870916-87-2
Purity:  99.53%
Target:  

ADC Linkers

Research Areas:  

Cancer

Mc- Val- Ala- PAB is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
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Cat. No.: HY-136136
CAS No.: 1394238-92-6
Purity:  98.90%
Target:  

ADC Linkers

Research Areas:  

Cancer

Fmoc-Val-Ala-PAB-PNP is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
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Cat. No.: HY-147271
CAS No.: 2679821-39-5
Purity:  99.48%
Research Areas:  

Others

Mal-PEG8-Val-Ala-PAB-Exatecan (Compound 9b) is an antibody-drug conjugate linker (ADC linker) that binds to Nectin-4 polypeptides conjugated to chemotherapeutic agents. Mal-PEG8-Val-Ala-PAB-Exatecan can be used for cancer research .
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Cat. No.: HY-101162
CAS No.: 1342820-51-2
Purity:  96.17%
Research Areas:  

Cancer

SGD-1910 is a agent-linker conjugate for ADC by using the antitumor antibiotic, pyrrolobenzodiazepine (PBD, a cytotoxic DNA crosslinking), linked via the cleavable linker MC-Val-Ala .
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Cat. No.: HY-136547
CAS No.: 1884577-99-4
Purity:  98.36%
Target:  

ADC Linkers

Research Areas:  

Others

Boc-Val-Ala-PAB is a cathepsin cleavable ADC linker that is used for making antibody-drug conjugate (ADCs) .
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Cat. No.: HY-126353
CAS No.: 1394238-91-5
Purity:  99.88%
Target:  

ADC Linkers

Research Areas:  

Cancer

Fmoc-Val-Ala-PAB-OH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
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Cat. No.: HY-135975
CAS No.: 1639939-40-4
Purity:  99.51%
Target:  

ADC Linkers

Research Areas:  

Cancer

MC-Val-Ala-PAB-PNP is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
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Cat. No.: HY-125933
CAS No.: 1343476-44-7
Purity:  99.12%
Target:  

ADC Linkers

Research Areas:  

Cancer

Val-Ala-PAB is a cleavable ADC linker that can be used for ADCs synthesis .
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Cat. No.: HY-171580
Research Areas:  

Cancer

Mc-PEG4-Val-Ala-PAB-Exatecan is a Drug-linker conjugate for ADC. Mc-PEG4-Val-Ala-PAB-Exatecan contains the ADC linker (Mc-PEG4-Val-Ala-PAB) and a DNA topoisomerase I inhibitor Exatecan (HY-13631) .
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Cat. No.: HY-101152
CAS No.: 1595275-61-8
Purity:  96.89%
Research Areas:  

Cancer

SG3199-Val-Ala-PAB is an intermediate of Tesirine synthesis. Tesirine is a agent-linker conjugate for ADC which can be used for the research of several cancers .
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Cat. No.: HY-W071967
CAS No.: 1343407-91-9
Target:  

ADC Linkers

Research Areas:  

Cancer

Alloc-Val-Ala-PAB is a peptide cleavable linker used in the synthesis of antibody-drug conjugates (ADCs). The Val-Ala will specifically be cleaved by Cathepsin B. The Alloc group is stable to treatment with piperidine and TFA, but can be easily removed under mild conditions by palladium catalyzed allyl transfer.
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Cat. No.: HY-W106311
CAS No.: 150114-97-9
Target:  

Drug Intermediate

Research Areas:  

Cancer

Fmoc-Val-Ala-OH is an intermediate for synthesizing the ADC linker. Fmoc-Val-Ala-OH can be used for the research of cancer .
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Cat. No.: HY-153032
CAS No.: 1912408-92-4
Purity:  98.89%
Research Areas:  

Cancer

Val-Ala-PAB-MMAE is a Drug-Linker Conjugate for ADC, consisting of ADC linker (Val-Ala-PAB) and MMAE. MMAE is an effective inhibitor of tubulin.
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