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BIIB 021, Tocris Bioscience™ Available on GSA/VA Contract for Federal Government customers only.

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Quantity:
10mg
50mg
This item is not returnable. View return policy
848695-25-0
C14H15ClN6O
318.765
QULDDKSCVCJTPV-UHFFFAOYSA-N
biib021,6-chloro-9-4-methoxy-3,5-dimethylpyridin-2-yl methyl-9h-purin-2-amine,biib 021,biib-021,unii-851b9fq7q0,6-chloro-9-4-methoxy-3,5-dimethylpyridin-2-yl methyl purin-2-amine,6-chloro-9-4-methoxy-3,5-dimethyl-2-pyridinyl methyl-9h-purin-2-amine,3qdd
16736529
6-chloro-9-[(4-methoxy-3,5-dimethylpyridin-2-yl)methyl]purin-2-amine
CC1=CN=C(C(=C1OC)C)CN2C=NC3=C2N=C(N=C3Cl)N
This item is not returnable. View return policy
848695-25-0
C14H15ClN6O
318.765
QULDDKSCVCJTPV-UHFFFAOYSA-N
biib021,6-chloro-9-4-methoxy-3,5-dimethylpyridin-2-yl methyl-9h-purin-2-amine,biib 021,biib-021,unii-851b9fq7q0,6-chloro-9-4-methoxy-3,5-dimethylpyridin-2-yl methyl purin-2-amine,6-chloro-9-4-methoxy-3,5-dimethyl-2-pyridinyl methyl-9h-purin-2-amine,3qdd
16736529
6-chloro-9-[(4-methoxy-3,5-dimethylpyridin-2-yl)methyl]purin-2-amine
CC1=CN=C(C(=C1OC)C)CN2C=NC3=C2N=C(N=C3Cl)N

Selective Hsp90 inhibitor

Selective, Hsp90 competitive inhibitor (Ki = 1.7 nM). Displays no significant activity at a range of ATP-binding kinases or Na+K+ ATPase. Induces degradation of HER-2 in vitro (EC50 = 38 nM in MCF-7 cells). Inhibits growth and promotes cell death in a variety of human tumor cells. Orally bioavailable.

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Quantity 10mg
Formula Weight 318.76
Percent Purity >98%
Chemical Name or Material BIIB 021

Recommended Storage : Store at -20°C