ADC Cytotoxin
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ADC Cytotoxin are a large collection of toxins for antibody-drug conjugate (ADC) development projects. The toxins that can be used as payloads should be soluble, amenable to conjugation, and stable. There are myriads of cellular toxins in natural or synthesized, but only a few have been found adaptable for an ADC concept.
The toxins targeting tubulin filaments include Maytansinoids, Auristatins, Taxol derivatives, etc. Amatoxins are a class of transcription-inhibiting agents. They bind to RNA polymerase II, leading to cell apoptosis. Protein toxins function in the similar MOA (mechanism of action) with cellular toxins, they could inhibit protein synthesis and induce cell death. While enzyme-based ADCs alter the microenvironment of disease tissues to disturb their functions.
Products Related to ADC Cytotoxin(111)
- GC69091Exatecan Intermediate 2CAS: 182182-31-6Purity: >99.00%
Exatecan Intermediate 2 (compound B) is an intermediate compound in the production of Exatecan (DX-8951), which is an anticancer agent and belongs to the camptothecin analogs. It interferes with tumor cell proliferation and division by interacting with DNA, thereby inhibiting tumor growth. Exatecan is mainly used for research on various cancers such as ovarian cancer, lung cancer, and breast cancer.
- GC69278InebilizumabCAS: 1299440-37-1Purity: >95.00%
Inebilizumab is a monoclonal antibody (mAb) that targets CD19 and enhances antibody-dependent cell-mediated cytotoxicity against B cells. Inebilizumab is being studied for use in multiple sclerosis and neuromyelitis optica spectrum disorder.
- GC69438Maytansinoid BCAS: 1628543-40-7Purity: >98%
Maytansinoid B is an ADC cytotoxin that can form Antibody-Drug Conjugates (ADCs) when coupled with antibodies. Maytansinoids are known anti-mitotic agents that bind to tubulin and inhibit microtubule assembly. Maytansinoids can induce cell cycle arrest at G2/M phase, thereby inducing apoptosis.
- GC70043Tomaymycin DMCAS: 945490-09-5Purity: >98%
Tomaymycin DM is a DNA alkylating agent and a derivative of Tomaymycin. It is a monomer of PBD and can serve as an effective payload for tumor-targeting antibody-drug conjugates (ADCs).
- GC71030Glucocorticoid receptor agonist-2CAS: 2166378-92-1Purity: >99.00%
Glucocorticoid receptor agonist-2 (compound 21) is an glucocorticoid receptor agonist with an IC50 value of 6.6 nM.
- GC71458Glucocorticoid receptor agonist-3CAS: 2842165-73-3Purity: >98.00%
Glucocorticoid receptor agonist-3 (Preparation 6) is a glucocorticoid receptor agonist.
- GC730137-Aminomethyl-10-methyl-11-fluoro camptothecinCAS: 2378616-23-8Purity: >99.00%
7-Aminometl-10-metl-11-fluoro camptothecin is a cytotoxin of MC-AAA-NHCH2OCH2COO-7-aminometl-10-metl-11-fluoro camptothecin.
- GC730147-Aminomethyl-10-methyl-11-fluoro camptothecin TFAPurity: >96.00%
7-Aminometl-10-metl-11-fluoro camptothecin TFA is a cytotoxin of MC-AAA-NHCH2OCH2COO-7-aminometl-10-metl-11-fluoro camptothecin.
- GC730157-MAD-MDCPTCAS: 765871-81-6Purity: >98.00%
7-MAD-MDCPT, a Camptothecin analog, is a toxin payload in antibody drug conjugates (ADCs).
- GC73056(1S,9R)-Exatecan mesylateCAS: 2938875-54-6Purity: >98.00%
(1S,9R)-Exatecan mesylate ((1S,9R)-DX8951f) is an isomer of Exatecan mesylate.
- GC73057(1R,9R)-Exatecan mesylateCAS: 2938875-39-7Purity: >99.00%
(1R,9R)-Exatecan mesylate((1R,9R)-DX8951f) is an isomer of Exatecan mesylate.
- GC73204NH2-bicyclo[1.1.1]pentane-7-MAD-MDCPT hydrochloridePurity: >95.00%
NH2-bicyclo[1.1.1]pentane-7-MAD-MDCPT drochloride is a topoisomerase I inhibitor, which can be delivered to cells through conjugated antibody targeting, and has good ADC activity in vivo and in vitro.
- GC73419Decyclohexanamine-ExatecanCAS: 2505045-51-0Purity: >98.00%
Decyclohexanamine-Exatecan is a Camptothecin derivative, compound a, extracted from patent WO2020219287 A1.
- GC736547-Hydroxyethyl carbamate-(10Me-11F-Camptothecin)CAS: 2873460-17-2Purity: >98.00%
7-droxyetl carbamate-(10Me-11F-Camptothecin) is a Camptothecin analogue.
- GC73669Cyclopropaneacetamide-ExatecanCAS: 2414254-36-5Purity: >97.00%
Cyclopropaneacetamide-Exatecan (Compound 2-A) is an ADC Cytotoxin and an Exatecan analogue.
- GC73670(αR)-Cyclopropaneacetamide-ExatecanCAS: 2414254-37-6Purity: >99.00%
(αR)-Cyclopropaneacetamide-Exatecan (compound 2-A), an Exenotecan derivative, is a cytotoxic agent.
- GC73685NH2-methylpropanamide-Exatecan TFACAS: 1817857-35-4
NH2-metlpropanamide-Exatecan TFA is a metlpropanamide-modified Exatecan , which is the common ADC Cytotoxin used in the synthesis of ADC.
- GC736947-Hydroxymethyl-10,11-MDCPT-d5Purity: >97.00%
7-droxymetl-10,11-MDCPT-d5 is deuterium labeled 7-droxymetl-10,11-MDCPT, which is a is a payload that can be used for ADC synthesis.
- GC73711Exatecan-methylacetamide-OHCAS: 2594423-51-3Purity: >97.00%
Exatecan-metlacetamide-OH (compound 6) is a Exatecan derivative with anticancer effects.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC69091 | Exatecan Intermediate 2 | 182182-31-6 | >99.00% | |
Exatecan Intermediate 2 (compound B) is an intermediate compound in the production of Exatecan (DX-8951), which is an anticancer agent and belongs to the camptothecin analogs. It interferes with tumor cell proliferation and division by interacting with DNA, thereby inhibiting tumor growth. Exatecan is mainly used for research on various cancers such as ovarian cancer, lung cancer, and breast cancer. | ||||
| GC69278 | Inebilizumab | 1299440-37-1 | >95.00% | |
Inebilizumab is a monoclonal antibody (mAb) that targets CD19 and enhances antibody-dependent cell-mediated cytotoxicity against B cells. Inebilizumab is being studied for use in multiple sclerosis and neuromyelitis optica spectrum disorder. | ||||
| GC69438 | Maytansinoid B | 1628543-40-7 | >98% | |
Maytansinoid B is an ADC cytotoxin that can form Antibody-Drug Conjugates (ADCs) when coupled with antibodies. Maytansinoids are known anti-mitotic agents that bind to tubulin and inhibit microtubule assembly. Maytansinoids can induce cell cycle arrest at G2/M phase, thereby inducing apoptosis. | ||||
| GC69863 | SC209 | 1977557-86-0 | >99.00% | |
SC209 is an ADC cytotoxin derived from patent WO2021247798, used for synthesizing anti-EGFR antibody-active molecule conjugated ADCs. SC209 is a metabolite of STRO-002. | ||||
| GC70043 | Tomaymycin DM | 945490-09-5 | >98% | |
Tomaymycin DM is a DNA alkylating agent and a derivative of Tomaymycin. It is a monomer of PBD and can serve as an effective payload for tumor-targeting antibody-drug conjugates (ADCs). | ||||
| GC71030 | Glucocorticoid receptor agonist-2 | 2166378-92-1 | >99.00% | |
Glucocorticoid receptor agonist-2 (compound 21) is an glucocorticoid receptor agonist with an IC50 value of 6.6 nM. | ||||
| GC71057 | S-Me-DM4 | 890654-03-2 | >99.00% | |
S-Me-DM4 is a metabolite of DM4 S-methylated by intracellular enzyme. | ||||
| GC71458 | Glucocorticoid receptor agonist-3 | 2842165-73-3 | >98.00% | |
Glucocorticoid receptor agonist-3 (Preparation 6) is a glucocorticoid receptor agonist. | ||||
| GC73013 | 7-Aminomethyl-10-methyl-11-fluoro camptothecin | 2378616-23-8 | >99.00% | |
7-Aminometl-10-metl-11-fluoro camptothecin is a cytotoxin of MC-AAA-NHCH2OCH2COO-7-aminometl-10-metl-11-fluoro camptothecin. | ||||
| GC73014 | 7-Aminomethyl-10-methyl-11-fluoro camptothecin TFA | - | >96.00% | |
7-Aminometl-10-metl-11-fluoro camptothecin TFA is a cytotoxin of MC-AAA-NHCH2OCH2COO-7-aminometl-10-metl-11-fluoro camptothecin. | ||||
| GC73015 | 7-MAD-MDCPT | 765871-81-6 | >98.00% | |
7-MAD-MDCPT, a Camptothecin analog, is a toxin payload in antibody drug conjugates (ADCs). | ||||
| GC73056 | (1S,9R)-Exatecan mesylate | 2938875-54-6 | >98.00% | |
(1S,9R)-Exatecan mesylate ((1S,9R)-DX8951f) is an isomer of Exatecan mesylate. | ||||
| GC73057 | (1R,9R)-Exatecan mesylate | 2938875-39-7 | >99.00% | |
(1R,9R)-Exatecan mesylate((1R,9R)-DX8951f) is an isomer of Exatecan mesylate. | ||||
| GC73154 | TAM470 | 1802498-63-0 | >98.00% | |
TAM470 is a novel cytolysin, inhibiting tubulin polymerization and microtubule depolymerization. | ||||
| GC73204 | NH2-bicyclo[1.1.1]pentane-7-MAD-MDCPT hydrochloride | - | >95.00% | |
NH2-bicyclo[1.1.1]pentane-7-MAD-MDCPT drochloride is a topoisomerase I inhibitor, which can be delivered to cells through conjugated antibody targeting, and has good ADC activity in vivo and in vitro. | ||||
| GC73419 | Decyclohexanamine-Exatecan | 2505045-51-0 | >98.00% | |
Decyclohexanamine-Exatecan is a Camptothecin derivative, compound a, extracted from patent WO2020219287 A1. | ||||
| GC73622 | MMAF-OtBu | 745017-95-2 | - | |
MMAF-OtBu (Example 2) is a modified MMAF. | ||||
| GC73654 | 7-Hydroxyethyl carbamate-(10Me-11F-Camptothecin) | 2873460-17-2 | >98.00% | |
7-droxyetl carbamate-(10Me-11F-Camptothecin) is a Camptothecin analogue. | ||||
| GC73669 | Cyclopropaneacetamide-Exatecan | 2414254-36-5 | >97.00% | |
Cyclopropaneacetamide-Exatecan (Compound 2-A) is an ADC Cytotoxin and an Exatecan analogue. | ||||
| GC73670 | (αR)-Cyclopropaneacetamide-Exatecan | 2414254-37-6 | >99.00% | |
(αR)-Cyclopropaneacetamide-Exatecan (compound 2-A), an Exenotecan derivative, is a cytotoxic agent. | ||||
| GC73685 | NH2-methylpropanamide-Exatecan TFA | 1817857-35-4 | - | |
NH2-metlpropanamide-Exatecan TFA is a metlpropanamide-modified Exatecan , which is the common ADC Cytotoxin used in the synthesis of ADC. | ||||
| GC73694 | 7-Hydroxymethyl-10,11-MDCPT-d5 | - | >97.00% | |
7-droxymetl-10,11-MDCPT-d5 is deuterium labeled 7-droxymetl-10,11-MDCPT, which is a is a payload that can be used for ADC synthesis. | ||||
| GC73711 | Exatecan-methylacetamide-OH | 2594423-51-3 | >97.00% | |
Exatecan-metlacetamide-OH (compound 6) is a Exatecan derivative with anticancer effects. | ||||
| GC73713 | FL118-14-Propanol | 2821768-98-1 | >98.00% | |
FL118-14-Propanol is a FL118 derivative. | ||||
