WAY-100635 maleate salt 100mg 100mg | Purity Not Available
Adooq Bioscience
WAY-100635 maleate is a potent and selective 5-hydroxytryptamine1A antagonist with an IC50 of 0.95 – 0.12 nM for 5-HT.
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WAY-100635 maleate salt 10mg 10mg | Purity Not Available
Adooq Bioscience
WAY-100635 maleate is a potent and selective 5-hydroxytryptamine1A antagonist with an IC50 of 0.95 – 0.12 nM for 5-HT.
More Information Supplier PageVTP-27999 2,2,2-trifluoroacetate 50mg 50mg | Purity Not Available
Adooq Bioscience
VTP-27999 2,2,2-trifluoroacetate is an alkyl amine Renin inhibitor; VTP-27999 is useful for Hypertension and End-Organ Diseases.
More Information Supplier PageVTP-27999 2,2,2-trifluoroacetate 100mg 100mg | Purity Not Available
Adooq Bioscience
VTP-27999 2,2,2-trifluoroacetate is an alkyl amine Renin inhibitor; VTP-27999 is useful for Hypertension and End-Organ Diseases.
More Information Supplier PageVTP-27999 2,2,2-trifluoroacetate 10mg 10mg | Purity Not Available
Adooq Bioscience
VTP-27999 2,2,2-trifluoroacetate is an alkyl amine Renin inhibitor; VTP-27999 is useful for Hypertension and End-Organ Diseases.
More Information Supplier PageVoreloxin Hydrochloride 5mg 5mg | Purity Not Available
Adooq Bioscience
Voreloxin Hcl is a small molecule and a naphthyridine analogue with antineoplastic activity; inhibitor of Topo II.
More Information Supplier PageVoreloxin Hydrochloride 25mg 25mg | Purity Not Available
Adooq Bioscience
Voreloxin Hcl is a small molecule and a naphthyridine analogue with antineoplastic activity; inhibitor of Topo II.
More Information Supplier PageVoreloxin Hydrochloride 10mg 10mg | Purity Not Available
Adooq Bioscience
Voreloxin Hcl is a small molecule and a naphthyridine analogue with antineoplastic activity; inhibitor of Topo II.
More Information Supplier PageXL-147 10mg 10mg | Purity Not Available
Adooq Bioscience
XL147 is a potent, orally bioavailable inhibitor of the class I PI3K family of lipid kinases.
More Information Supplier PageXL-147 25mg 25mg | Purity Not Available
Adooq Bioscience
XL147 is a potent, orally bioavailable inhibitor of the class I PI3K family of lipid kinases.
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