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ADC Cytotoxin
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ADC Cytotoxin

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Catalog Product Name CAS Number
BADC-01400 Seco-DUBA 1227961-59-2
seco-DUBA hydrochloride is a cell-permeable pro-drug that is cleaved into the active toxin (DUBA) in intracellular lysosomes by proteases, after internalization. The payload then alkylates the DNA, causing DNA damage and cell death. 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-00015 MC-Val-Ala-PBD 1342820-51-2
MC-Val-Ala-PBD is a protective group conjugated PBD, PBD bind in the minor groove of DNA. Inquiry
BADC-00017 DM4-SMCC 1228105-52-9
DM4 with a reactive linker SMCC, which can react with antibody to make antibody drug conjugate. DM4 can bind to tubulin at or near the vinblastine-binding site. Inquiry
BADC-00026 Mc-MMAD 1401963-15-2
Monomethyl auristatin D (MMAD), a potent tubulin inhibitor, is a toxin payload in antibody drug conjugate; Mc-MMAD is a protective group (maleimidocaproyl) -conjugated MMAD. Inquiry
BADC-00027 INNO-206 1361644-26-9
INNO-206 (Aldoxorubicin) is the 6-maleimidocaproyl hydrazone derivative prodrug of the anthracycline antibiotic doxorubicin (DOXO-EMCH) with antineoplastic activity. Inquiry
BADC-00028 DOXO-EMCH 151038-96-9
DOXO-EMCH is an albumin-binding prodrug of doxorubicin, which is an anthracycline antibiotic with anti-Gram-positive bacterial activity and a broad antitumor spectrum. Inquiry
BADC-00032 PF-06380101 1436391-86-4
PF-06380101 is a novel cytotoxic Dolastatin 10 analogue; with excellent potencies in tumor cell proliferation assays and differential ADME properties when compared to other synthetic auristatin analogues that are used in the preparation of ADCs. Inquiry
BADC-00034 Taltobulin 228266-40-8
Taltobulin, also known as HTI-286 and SPA-110, is a fully synthetic analog of the natural tripeptide hemiasterlin, inhibits tubulin polymerization and circumvents transport-based resistance to taxanes. HTI-286 was a potent inhibitor of proliferation (mean IC50 = 2.5 ± 2.1 nm in 18 human tumor cell lines) and had substantially less interaction with multidrug resistance protein (P-glycoprotein) than currently used antimicrotubule agents, including paclitaxel, docetaxel, vinorelbine, or vinblastine. Inquiry
BADC-00035 Taltobulin trifluoroacetate 228266-41-9
Taltobulin trifluoroacetate is a potent antimicrotubule agent that circumvents P-glycoprotein-mediated resistance in vitro and in vivo. Taltobulin trifluoroacetate inhibits the polymerization of purified tubulin, disrupts microtubule organization in cells, and induces mitotic arrest, as well as apoptosis. Inquiry
BADC-00039 Doxorubicin 23214-92-8
Doxorubicin is an anthracycline antibiotic produced in Str. peucetius var. caesinus. Doxorubicin has anti-Gram-positive bacteria activity and has a broad anti-tumor spectrum. Doxorubicin is an antibiotic agent that inhibits DNA topoisomerase II and induces DNA damage and apoptosis. Inquiry
BADC-00043 Daun02 290304-24-4
Daun02 is a daunorubicin b-galactoside prodrug for use in conjunction. Inquiry
BADC-00081 Ungerine Nitrate
Alkaloid , from plants of the Ungernia genus, Amaryllidaceae. Inquiry
BADC-00087 Maytansinoid DM4 799840-96-3
DM4 is a cytotoxic agent. It is used as the cytotoxic component in antibody-drug conjugates. 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
BADC-00179 Colcemide 477-30-5
An antineoplastic alkaloid from Colchicum autumnale L. isolated from Colchicum autumnale L. Inquiry
BADC-00186 Adaphotris
Inhibitor of Ca2+/2H+-exchange system in liver mitochondria. , synthetic. Inquiry
BADC-00190 7-Xylosyl-10-deacetyltaxol 90332-63-1
10-Deacetyl-7-xylosyl paclitaxel is a Paclitaxel derivative with improved pharmacological features and higher water solubility. Inquiry
BADC-00223 Duocarmycin A 118292-34-5
It is produced by the strain of (Pyridamycin) Streptomyces sp. DO-88. It has strong antibacterial and antitumor activity. It can inhibit gram-positive bacteria such as Staphylococcus aureus and Streptococcus faecalis (MIC is less than 0.01 μg/mL), it can also inhibit klebsiella pneumoniae (MIC is 0.032 μg/mL), other bacteria and yeast (MIC is 1-10 μg/mL). Inquiry
BADC-00243 14-Benzoyltalatisamine Perchlorate
A selective blocker of the delayed rectifier K+ channel found in virtual screening Inquiry
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