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Results for "

adccytotoxin

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    236
    TargetMol | Inhibitors_Agonists
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    4
    TargetMol | Peptide_Products
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    1
    TargetMol | Inhibitory_Antibodies
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Dxd
UNII-OQM5SD32BQ, OQM5SD32BQ, Exatecan derivative for ADC
T11249L1599440-33-1
Dxd (OQM5SD32BQ) is a potent DNA topoisomerase I inhibitor (IC50= 0.31 μM). Dxd was used as a conjugate drug for HER2-targeted ADCs.
  • $39
In Stock
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TargetMol | Inhibitor Hot
Thailanstatin A
T388891426953-21-0
Thailanstatin A is an ultra-potent inhibitor of eukaryotic RNA splicing (IC50 = 650 nM). It inhibits multiple cancer cell lines via non-covalent binding to the SF3b subunit of the U2 snRNA subcomplex of the spliceosome, displaying low-nM to sub-nM IC50s. Thailanstatin A, as a payload for ADCs, is conjugated to the lysines on trastuzumab, yielding linker-less ADC.
  • $187
In Stock
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TargetMol | Inhibitor Hot
Monomethyl auristatin E
Vedotin, MMAE
T6897474645-27-7
Monomethyl auristatin E (MMAE) (MMAE), an antimitotic agent, inhibits cell division by blocking the polymerization of tubulin and also has inhibition of antibody-drug conjugates (ADCs) activity.
  • $41
In Stock
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Duocarmycin TM
T11120157922-77-5
Duocarmycin TM is a DNA alkylator. Duocarmycin TM is an exceptionally potent antitumor antibiotic.
  • $158
In Stock
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MMAF-OMe
Monomethyl auristatin F methyl ester
T12081863971-12-4
MMAF-OMe (Monomethyl auristatin F methyl ester) is an antitubulin agent which inhibits several tumor cell lines with IC50s of 0.056 nM, 0.166 nM, 0.183 nM, and 0.449 nM for MDAMB435/5T4, MDAMB361DYT2, MDAMB468, and Raji (5T4-) cell lines, respectively. MMAF-Ome is also an ADC cytotoxin.
  • $34
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Auristatin F
T14349163768-50-1
Auristatin F is an effective inhibitor of microtubule and vascular damaging agent. Auristatin F can be used in antibody-drug conjugates.
  • $35
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Calicheamicin
Calicheamicin γ1
T14858108212-75-5
Calicheamicin (Calicheamicin γ1) is an antitumor antibiotic and is a DNA synthesis inhibitor. It also is a cytotoxic agent that causes double-strand DNA breaks.
  • $228
In Stock
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DM4
Ravtansine
T15141796073-69-3
DM4 (Ravtansine) can be used in the preparation of antibody drug conjugate and it is an antitubulin agent. It can inhibit cell division.
  • $31
In Stock
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PNU-159682
T16557202350-68-3
PNU-159682, a metabolite of anthracycline neomycin, is a DNA topoisomerase II inhibitor with excellent cytotoxicity.
  • $84
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Mertansine
Maytansinoid DM1, DM1
T1992139504-50-0
Mertansine is a tubulin inhibitor and an antibody-conjugable maytansinoid alkaloid. The IC50 of Mertansine against HCT-15 and A431 cells is 0.750 and 0.04nM.
  • $30
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MMAF
MonoMethyl auristatin F
T3256745017-94-1
MMAF (MonoMethyl auristatin F), an antimitotic agent, inhibits cell division by blocking the polymerization of tubulin.
  • $40
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MMAD
Monomethylauristatin D, Monomethyl Dolastatin 10, Demethyldolastatin 10
T4677203849-91-6
MMAD (Demethyldolastatin 10) is a potent tubulin inhibitor. MMAD is a toxin payload in antibody drug conjugates (ADCs).
  • $40
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Ansamitocin P 3'
Maytansinol butyrate, Antibiotic C 15003P3', Ansamitocin P-3
T191066547-09-9
Ansamitocin P 3' (Maytansinol butyrate) is an antibody-drug conjugate cytotoxin with antitumor activity.
  • $29
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Methotrexate disodium
T80037413-34-5
Methotrexate disodium is an tetrahydrofolate dehydrogenase inhibitor
  • $34
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CC-885-CH2-PEG1-NH-CH3
CC-885-CH2-PEG1-NH-CH3
T403432722698-03-3
CC-885-CH2-PEG1-NH-CH3 is a neoDegrader compound utilized in the synthesis of Antibody neoDegrader Conjugate (AnDC).
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