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Glycyl-H 1152 2HCl 5mg 5mg  | Purity Not Available

Adooq Bioscience

Glycyl-H 1152 2HCl is a selective and potent ROCK inhibitor (IC50 values are 0.0118, 2.35, 2.57, 3.26, > 10 and >10 uM for ROCKII, Aurora A, CAMKII, PKG, PKA and PKC respectively.)

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Glycyl-H 1152 2HCl 2mg 2mg  | Purity Not Available

Adooq Bioscience

Glycyl-H 1152 2HCl is a selective and potent ROCK inhibitor (IC50 values are 0.0118, 2.35, 2.57, 3.26, > 10 and >10 uM for ROCKII, Aurora A, CAMKII, PKG, PKA and PKC respectively.)

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Glycyl-H 1152 2HCl 1mg 1mg  | Purity Not Available

Adooq Bioscience

Glycyl-H 1152 2HCl is a selective and potent ROCK inhibitor (IC50 values are 0.0118, 2.35, 2.57, 3.26, > 10 and >10 uM for ROCKII, Aurora A, CAMKII, PKG, PKA and PKC respectively.)

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Quinupristin 50mg 50mg  | Purity Not Available

Adooq Bioscience

Quinupristin is a semi-synthetic analogue of virginiamycin B (ostreogyrcin B, pristinamycin IA, Streptogramin B) formed by a Mannich condensation and elimination to generate an exocyclic methylene alpha to the ketone of the 4-piperidinone.

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Quinupristin 25mg 25mg  | Purity Not Available

Adooq Bioscience

Quinupristin is a semi-synthetic analogue of virginiamycin B (ostreogyrcin B, pristinamycin IA, Streptogramin B) formed by a Mannich condensation and elimination to generate an exocyclic methylene alpha to the ketone of the 4-piperidinone.

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Quinupristin 10mg 10mg  | Purity Not Available

Adooq Bioscience

Quinupristin is a semi-synthetic analogue of virginiamycin B (ostreogyrcin B, pristinamycin IA, Streptogramin B) formed by a Mannich condensation and elimination to generate an exocyclic methylene alpha to the ketone of the 4-piperidinone.

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CL 316243 disodium salt 50mg 50mg  | Purity Not Available

Adooq Bioscience

CL 316243 disodium salt, a beta-3 adrenergic agonist, was developed as an anti-obesity and diabetes drug, and causes rapid decreases in blood glucose levels in mice.

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CL 316243 disodium salt 25mg 25mg  | Purity Not Available

Adooq Bioscience

CL 316243 disodium salt, a beta-3 adrenergic agonist, was developed as an anti-obesity and diabetes drug, and causes rapid decreases in blood glucose levels in mice.

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