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Chemical Structure Cat. No. Product Name CAS No.
Trovafloxacin Chemical Structure
BCP12644 Trovafloxacin 147059-72-1
Trovafloxacin is a broad spectrum antibiotic that inhibits the uncoiling of supercoiled DNA in various bacteria by blocking the activity of DNA gyrase and topoisomerase IV.
MKT-077 Chemical Structure
BCP30211 MKT-077 147366-41-4
MKT-077 is an inhibitor of mitochondrial hsp70 family member mortalin (mot-2), causing the selective death of cancer cells.
Aclarubicin Hydrochloride Chemical Structure
BCP07926 Aclarubicin Hydrochloride 75443-99-1
Aclarubicin hydrochloride is an anthracycline produced by Streptomyces galilaeus. It has potent antineoplastic activity.
Nimustine hydrochloride Chemical Structure
BCP11668 Nimustine hydrochloride 55661-38-6
Nimustine hydrochloride is a DNA alkylator and cross-linker. Anticancer agent used to treat malignant glioma. Cardiovascular teratogenicity was studied in rat fetuses.
Rubitecan Chemical Structure
BCP06207 Rubitecan 91421-42-0
Rubitecan is a semisynthetic agent related to camptothecin with potent antitumor and antiviral properties. Rubitecan binds to and inhibits the enzyme topoisomerase I and induces protein-linked DNA single-strand breaks, thereby blocking DNA and RNA synthesis in dividing cells; this agent also prevents repair of reversible single-strand DNA breaks.
Atuveciclib Racemate Chemical Structure
BCP30202 Atuveciclib Racemate 1414943-88-6
Atuveciclib Racemate is the racemate mixture of BAY-1143572. BAY-1143572 is a potent and highly selective, oral P-TEFb/CDK9 inhibitor which supresses CDK9/CycT1 with an IC50 of 13 nM.
CDK4-IN-1 Chemical Structure
BCP12704 CDK4-IN-1 1256963-02-6
CDK4-IN-1 is a selective inhibitor of cyclin-dependent kinase 4.
ACY-775 Chemical Structure
BCP30179 ACY-775 1375466-18-4
ACY-775 is a potent and selective inhibitor of the of histone deacetylase 6 (HDAC6) with an IC50 of 7.5 nM.
Bleomycin A5 Hydrochloride Chemical Structure
BCP12575 Bleomycin A5 Hydrochloride 55658-47-4
Bleomycin A5 is an anticancer chemotherapeutic that binds DNA and induces DNA cleavage and strand breaks, it is highly toxic.
Divalproex sodium Chemical Structure
BCP12800 Divalproex sodium 76584-70-8
Divalproex Sodium, consisting of a compound of sodium valproate and valproic acid in a 1:1 molar relationship in an enteric coated form, is a HDAC inhibitor, used in the treatment for epilepsy.
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