Acid-propionylamino-Val-Cit-OH ride (NLX-112 (hydrochloride)) Ginsenoside Ro (300 μM) inhibits

Ginsenoside Ro (300 μM) inhibits the thrombin-mediated elevation in TXB2 level by 94

In adult mice

Although fenoldopam was more potent than DA (EC50 55

IC50: ≥ 1 mM for Cdk5 Iso-Olomoucine is an inactive stereoisomer of the Cdk5 inhibitor olomoucine

Chemical Name: 2-(6-amino-2-{2-[6-amino-2-(6-amino-2-{6-amino-2-[(pyrrolidin-2-yl)formamido]hexanamido}hexanamido)hexanamido]-5-[(diaminomethylidene)amino]pentanamido}hexanamido)-3-methylbutanoic acid

Acid-propionylamino-Val-Cit-OH ride (NLX-112 (hydrochloride)) Ginsenoside Ro (300 μM) inhibitsAcid propionylamino Val Cit OH is a cleavable ADC linker used in the synthesis of antibody drug conjugates (ADCs). Product information CAS Number: 2098907 84 5 Molecular Weight: 374. 39 Formula: C15H26N4O7 Chemical Name: (2S) 5 (carbamoylamino) 2 [(2R) 2 (3 carboxypropanamido) 3 methylbutanamido]pentanoic acid Smiles: CC(C)[C@@H](NC(=O)CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=O)C(O)=O InChiKey: RBERRTKQXJAVGW JOYOIKCWSA N InChi: InChI=1S C15H26N4O7 c1 8(2)12(19