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Search Results for " val-val "

20

Compounds

Cat No. Product Name Synonyms Targets
T9227 Val-Ala-PAB Others
Val-Ala-PAB is a building block in the synthesis of Tesirine (a.k.a. SG3249), a clinical antibody-drug conjugate pyrrolobenzodiazepine dimer payload. Reagent in the preparation of pyrrolobenzodiazepine dimers and their a...
T18868 Val-Cit Others
Val-Cit is a cleavable ADC linker. Val-Cit is used in the synthesis of antibody-drug conjugates (ADCs).
T4289 Mc-​Val-​Ala-​PAB Mc-Val-Ala-PAB Others , AChR
Mc-Val-Ala-PAB, an effective linker, is utilized in antibody-drug-conjugate (ADC).
T4286 Fmoc-Val-Ala-PAB-OH Fmoc-Val-Ala-PAB Others , AChR
Fmoc-Val-Ala-PAB-OH (Fmoc-Val-Ala-PAB) is a useful linker for making Antibody-Drug-Conjugation (ADC) conjugate for targeting drug delivery. It is also utilized in the synthesis of RGD peptidomimetic-paclitaxel conjugates...
T4678 Fmoc-Val-Cit-PAB Others
Fmoc-Val-Cit-PAB is a linker for antibody-drug-conjugation (ADC).
TN6675 Cyclo(Pro-Val) Cyclo(prolylvalyl) Antibacterial , Antifungal
Cyclo(Pro-Val) (Cyclo(prolylvalyl)) is obtained from the marine fungus and shows moderate antifungal and weak antitumor activities. Cyclo(Pro-Val) inhibits the growth of Bacillus subtilis with MIC of 0.8 g/L.
T17693 Boc-Val-Cit-PAB Others
Boc-Val-Cit-PAB is a cleavable ADC linker. Boc-Val-Cit-PAB used in the synthesis of antibody-drug conjugates (ADCs).
T17213 Val-cit-PAB-OH Others
Val-cit-PAB-OH is an ADC linker that is cleavable.
T18867 Val-Cit-PAB-MMAE
Val-Cit-PAB-MMAE is a drug-linker conjugate for ADC. Val-Cit-PAB-MMAE contains the ADCs linker (peptide Val-Cit-PAB) and a potent tubulin inhibitor MMAE . MMAE a potent mitotic inhibitor by inhibiting tubulin polymerizat...
T17212 VAL-083 Dianhydrogalactitol,Dianhydrodulcitol DNA Alkylator/Crosslinker , DNA Alkylation
VAL-083 (Dianhydrogalactitol) is an alkylating compound that creates N7 methylation on DNA. It also has antitumor activity.
T17691 Boc-Val-Cit-OH Others
Boc-Val-Cit-OH is a cleavable ADC linker used in antibody-drug conjugates (ADCs) synthesis.
T7354 H-Val-Pro-Pro-OH RAAS
H-Val-Pro-Pro-OH is an inhibitor of Angiotensin I converting enzyme (ACE)( IC50 : 9 μM).
T17983 Fmoc-Val-Cit-PAB-MMAE Others
Fmoc-Val-Cit-PAB-MMAE is consisted of the ADCs linker (Fmoc-Val-Cit-PAB) and potent tubulin inhibitor (MMAE). Fmoc-Val-Cit-PAB-MMAE is a drug-linker conjugate for ADC.
T18318 MC-Val-Ala-PAB-PNP Others
MC-Val-Ala-PAB-PNP is a cleavable ADC linker. MC-Val-Ala-PAB-PNP can be used in the synthesis of antibody-drug conjugates (ADCs).
T17692 Boc-Val-Cit-PAB-PNP Others
Boc-Val-Cit-PAB-PNP is a cleavable ADC linker used in antibody-drug conjugates (ADCs) synthesis.
T7767 FMoc-Val-Cit-PAB-PNP Others
Fmoc-Val-Cit-PAB-PNP is a linker for Antibody-Drug-Conjugation (ADC).
T18321 Mc-Val-Cit-PAB-Cl Others
Mc-Val-Cit-PAB-Cl, a cleavable ADC linker, is utilized in the conjugation of MMAE and antibodies to produce compounds such as antibody-MC-vc-MMAE (e.g., anti-CD22-MC-VC-PABC-MMAE), which demonstrate cytotoxicity with IC5...
T18267 Mal-PEG1-Val-Cit-OH Others
Mal-PEG1-Val-Cit-OH is a cleavable one-unit polyethylene glycol (PEG) linker employed in the synthesis of antibody-drug conjugates (ADCs)[1].
T5149 MC-Val-Cit-PAB Others , AChR
MC-Val-Cit-PAB is a cathepsin cleavable ADC linker that is used for making antibody-drug conjugate. FDA approved drugs such as brentuximab vedotin use this linker.
T19350 H-Val-Ala-OH Valyl-alanine Endogenous Metabolite
H-Val-Ala-OH (Valyl-alanine) is a dipeptide formed from L-Valine and L-Alanine residues. It has a role as a metabolite. H-Val-Ala-OH is a dipeptide formed from L-Valine and L-Alanine residues.
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