ABT-046 10mg 10mg | Purity Not Available
Adooq Bioscience
ABT-046 is a potent, selective, and orally bioavailable Diacylglycerol acyltransferase 1 (DGAT-1 ) inhibitor (IC50= 8 nM).
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A 438079 hydrochloride 50mg 50mg | Purity Not Available
Adooq Bioscience
A 438079 Hcl is a competitive P2X7 receptor antagonist (pIC50 = 6.9 for the inhibition of Ca2+ influx in the human recombinant P2X7 cell line).
More Information Supplier PageA 438079 hydrochloride 25mg 25mg | Purity Not Available
Adooq Bioscience
A 438079 Hcl is a competitive P2X7 receptor antagonist (pIC50 = 6.9 for the inhibition of Ca2+ influx in the human recombinant P2X7 cell line).
More Information Supplier PageA 438079 hydrochloride 10mg 10mg | Purity Not Available
Adooq Bioscience
A 438079 Hcl is a competitive P2X7 receptor antagonist (pIC50 = 6.9 for the inhibition of Ca2+ influx in the human recombinant P2X7 cell line).
More Information Supplier Page9-Dihydro-13-acetylbaccatin III 5mg 5mg | Purity Not Available
Adooq Bioscience
9-Dihydro-13-acetylbaccatin III (9-DHAB III) is an intermediate for taxol analog preparations.
More Information Supplier Page9-Dihydro-13-acetylbaccatin III 25mg 25mg | Purity Not Available
Adooq Bioscience
9-Dihydro-13-acetylbaccatin III (9-DHAB III) is an intermediate for taxol analog preparations.
More Information Supplier Page9-Dihydro-13-acetylbaccatin III 10mg 10mg | Purity Not Available
Adooq Bioscience
9-Dihydro-13-acetylbaccatin III (9-DHAB III) is an intermediate for taxol analog preparations.
More Information Supplier Page7-xylosyltaxol 50mg 50mg | Purity Not Available
Adooq Bioscience
7-xylosyltaxol is a taxol derivative, Paclitaxel binds to tubulin and inhibits the disassembly of microtubules.
More Information Supplier PageABT-046 5mg 5mg | Purity Not Available
Adooq Bioscience
ABT-046 is a potent, selective, and orally bioavailable Diacylglycerol acyltransferase 1 (DGAT-1 ) inhibitor (IC50= 8 nM).
More Information Supplier PageAfatinib dimaleate 100mg 100mg | Purity Not Available
Adooq Bioscience
Afatinib is an irreversible EGFR/HER2 inhibitor with an IC50 of 14 nM for in vitro potency against HER2.
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