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Catalog Product Name CAS Number
BADC-00088 Nemorubicin 108852-90-0
Nemorubicin, is a doxorubicin derivative that differs significantly from its parent drug in terms of spectrum of antitumor activity, metabolism and toxicity profile. The drug is active on tumors resistant to alkylating agents, topoisomerase II inhibitors and platinum derivatives. Inquiry
BADC-00153 Chlorotoxin 163515-35-3
Chlorotoxin (Cltx) is a neurotoxin that was originally isolated from the venom of Leiurus quinquestriatus. Chlorotoxin is a specific ligand of glioma cells. Chlorotoxin binds to Cl- channels (small conductance epithelial chloride channels) in the brain and spinal cord and inhibits Cl- influx. Inquiry
BADC-00182 Duocarmycin analog
Duocarmycin analog has cytotoxicity for solid tumor cells that can be used for antibody-drug conjugates (ADCs). Duocarmycins and the analogs acts via binding to the minor groove of DNA and alkylating the nucleobase adenine at the N3 position, which leads to DNA damage and cancer cell death. Inquiry
BADC-00253 Luteolin 7-O-glucoside 5373-11-5
Cynaroside is a flavone, a flavonoid-like chemical compound. It is a 7-O-glucoside of luteolin. Inquiry
BADC-00266 Galantamine hydrobromide 1953-04-4
Galantamine hydrobromide is a long-acting, centrally active acetylcholinesterase inhibitor (IC50 = 410 nM) and allosteric potentiator at neuronal nicotinic ACh receptors. It prevents β-amyloid-induced apoptosis in SH-SY5Y and bovine chromaffin cells. Inquiry
BADC-00290 Lycorine hydrochloride 2188-68-3
Lycorine is a toxic crystalline alkaloid found in various Amaryllidaceae species, such as the cultivated bush lily , surprise lilies, and daffodils. It may be highly poisonous, or even lethal, when ingested in certain quantities. Symptoms of lycorine toxicity are vomiting, diarrhea, and convulsions. Inquiry
BADC-00330 Irofulven 158440-71-2
Irofulven is a semisynthetic sesquiterpene derivative of illudin S, a natural toxin isolated from the fungus Omphalotus illudens. Irofulven alkylates DNA and protein macromolecules, forms adducts, and arrests cells in the S-phase of the cell cycle. Inquiry
BADC-00335 DC-1
DC-1 is a cytotoxic agent, used as the cytotoxic component in antibody-drug conjugates. Inquiry
BADC-00343 Seco-Duocarmycin MB
Seco-Duocarmycin MB is a cytotoxic agent, used as the cytotoxic component in antibody-drug conjugates. Inquiry
BADC-00346 Maytansine 35846-53-8
Maitansine, a cytotoxic agent, inhibits the assembly of microtubules by binding to tubulin at the rhizoxin binding site. Inquiry
BADC-00360 Tubulysin M 936691-46-2
Tubulysin M is a Tubulysin D analog with potential anti-cancer properties, used as the cytotoxic component in antibody-drug conjugates. Inquiry
BADC-00361 Combretastatin A4 117048-59-6
Combretastatin A4 is a stilbenoid isolated from Combretum caffrum. Combretastatin A4 was shown to inhibit tubulin polymerization (IC50 = 2.2 μM). It has demonstrable antineoplastic activity. Inquiry
BADC-00775 FR-901464 146478-72-0
It is a potent cell cycle inhibitor isolated from Pseudomonas sp. No.2663. It exhibits potent antitumor activities against tumor cell lines via binding to the spliceosome and modulating pre-mRNA splicing. Inquiry
BADC-00790 Mithramycin A 18378-89-7
Mithramycin A is an antineoplastic antibiotic produced by Streptomyces plicatus. Mithramycin A is a polymerase inhibitor that binds to GC rich sequences located in the minor groove of DNA. Inquiry
BADC-00791 Illudin S 1149-99-1
Illudin S is a natural sesquiterpene agent with strong anti-tumour activity. Illudin S inhibits DNA synthesis via an unknown mechanism. Inquiry
BADC-00798 Actinomycin D 50-76-0
Actinomycin D is a chromopeptide antineoplastic antibiotic that exhibits high antibacterial and antitumor activity. Actinomycin D binds to single- and double-stranded DNA and subsequent inhibition of RNA and protein synthesis. Inquiry
BADC-00800 Exatecan Mesylate 169869-90-3
Exatecan mesylate is a semisynthetic, water-soluble derivative of camptothecin with antineoplastic activity. Exatecan mesylate inhibits topoisomerase I activity by stabilizing the cleavable complex between topoisomerase I and DNA and inhibiting the religation of DNA breaks, thereby inhibiting DNA replication and triggering apoptotic cell death. This agent does not require enzymatic activation and exhibits greater potency than camptothecin and other camptothecin analogs. Inquiry
BADC-00001 CBT-161
CBT-161 is an ADC that STI-A0602, the monoclonal antibody targeting c-Met, links tubulin inhibitors or DNA damaging agents via C-lock. Preclinical study showed that CBT-161 significantly inhibited tumor growth. Inquiry
BADC-00081 Ungerine Nitrate
Alkaloid , from plants of the Ungernia genus, Amaryllidaceae. Inquiry
BADC-00129 Pentazolone hydrochloride 21314-60-3
Synthetic, an inhibitor of monoamine oxydase.Enhances the toxicity of the Phenamine group and of Tryptamine. Inquiry
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