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Carbamic acid, [(3-amino-1H-indazol-5-yl)methyl]-, 1,1-dimethylethyl ester, also known as indibulin, is a synthetic chemical compound with potential antineoplastic activity. It is a derivative of a tubulin-inhibitor drug that disrupts microtubule dynamics, leading to cell cycle arrest and apoptosis in cancer cells. Indibulin has shown promising results in preclinical studies and early-stage clinical trials for its potential use in the treatment of various types of cancer, including breast, prostate, and non-small cell lung cancer. Its mechanism of action and potential therapeutic applications make it a promising candidate for further research and development as a potential anti-cancer drug.

368426-90-8

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368426-90-8 Usage

Uses

Used in Pharmaceutical Industry:
Indibulin is used as an antineoplastic agent for its potential use in the treatment of various types of cancer, including breast, prostate, and non-small cell lung cancer. It disrupts microtubule dynamics, leading to cell cycle arrest and apoptosis in cancer cells, making it a promising candidate for further research and development as a potential anti-cancer drug.

Check Digit Verification of cas no

The CAS Registry Mumber 368426-90-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,8,4,2 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 368426-90:
(8*3)+(7*6)+(6*8)+(5*4)+(4*2)+(3*6)+(2*9)+(1*0)=178
178 % 10 = 8
So 368426-90-8 is a valid CAS Registry Number.

368426-90-8Downstream Products

368426-90-8Relevant articles and documents

Non-covalent thrombin inhibitors featuring P3-heterocycles with P1-bicyclic arginine surrogates

Cui, Jingrong Jean,Araldi, Gian-Luca,Reiner, John E.,Reddy, Komandla Malla,Kemp, Scott J.,Ho, Jonathan Z.,Siev, Daniel V.,Mamedova, Lala,Gibson, Tony S.,Gaudette, John A.,Minami, Nathaniel K.,Anderson, Susanne M.,Bradbury, Annette E.,Nolan, Thomas G.,Semple

, p. 2925 - 2930 (2007/10/03)

Novel, potent, and highly selective classes of thrombin inhibitors were identified, which resulted from judicious combination of P4-aromatics and P2-P3-heterocyclic dipeptide surrogates with weakly basic (calcd pKa ~non-basic - 8.6) bicyclic P1-arginine mimics. The design, synthesis, and biological activity of achiral, non-covalent, orally bioavailable inhibitors NC1-NC44 featuring P1-indazoles, benzimidazoles, indoles, benzotriazoles, and aminobenzisoxazoles is disclosed.

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