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AZD2014 analytical pure 0.993

AZD2014 is an mTOR inhibitor with IC50 of 2.8 nM and is highly selective against multiple PI3K isoforms (α/β/γ/δ).

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AZD5363 analytical pure 0.996

AZD5363 is a potent pan-AKT kinase inhibitor with IC50 of 3, 7 and 7 nM for Akt1,Akt2 and Akt3, respectively.

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AZD6738 analytical pure 0.994

AZD6738 is a highly selective and potent inhibitor of ATR kinase activity with IC50 value of 1nM in isolated enzyme assay and showed inhibitory effect on ATR kinase-dependent cellular Chk1 phosphorylation with IC50 value of 74nM.

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AZD7762 analytical pure 0.999

AZD7762 is a potent and selective inhibitor of Chk1 with IC50 of 5 nM, being equally potent against Chk2 and less potent against CAM, Yes, Fyn, Lyn, Hck and Lck.

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AZD8186 analytical pure 0.999

AZD8186 is an isoform-specific small-molecule PI3K inhibitor, potently inhibits PI3Kβ (IC50=4 nM) and PI3Kδ (IC50=12 nM) with selectivity over PI3Kα (IC50=35 nM) and PI3Kγ (IC50=675 nM).

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Amitriptyline Hydrochloride

Amitriptyline Hydrochloride is an antidepressant with sedative effects. Its mechanism of action in man is not known. Amitriptyline Hydrochloride is not a monoamine oxidase inhibitor and it does not act primarily by stimulation of the central nervous system.

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BLU9931 analytical pure 0.999

BLU9931 is an inhibitor of FGFR4 with IC50 of 3 nM and is less potent for FGFR1/2/3 (IC50 > 150 nM).

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BMN-673 analytical pure 0.999

BMN-673 is a PARP1/2 inhibitor with IC50 of 0.57 nM for PARP1.

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BSI-201 analytical pure 0.978

BSI-201 is a PARP1 inhibitor with demonstrated effectiveness in triple-negative breast cancer (TNBC).

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Beclomethasone Dipropionate

Beclomethasone Dipropionate is a steroid ester comprising beclomethasone having propionyl groups at the 17- and 21-positions. It has a role as an anti-inflammatory drug, an anti-asthmatic drug, a prodrug and an anti-arrhythmia drug.

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