Laboratory

Butaprost is a structural analog of PGE2 with good selectivity for the EP2 receptor subtype. Butaprost has frequently been used to pharmacologically define the EP receptor expression profile of various human and animal tissues and cells.

Butaprost is a structural analog of PGE2 with good selectivity for the EP2 receptor subtype. Butaprost has frequently been used to pharmacologically define the EP receptor expression profile of various human and animal tissues and cells.

Butaprost is a structural analog of PGE2 with good selectivity for the EP2 receptor subtype. Butaprost has frequently been used to pharmacologically define the EP receptor expression profile of various human and animal tissues and cells.

A stereoisomer of CCG-1423 that less potently inhibits MRTF-A-dependent cellular events, including SRF-mediated gene expression and cell migration.

Purity Limit: &ge 98% (HPLC) CAS No.: 210488-55-4 Molecular Formula: C9H11NO·HCl Molecular Weight: 185.65 MDL No.: MFCD08457629 Appearance: White powder Storage Temperature: Store at 0-8 °C

Purity Limit: &ge 98% (HPLC) CAS No.: 210488-55-4 Molecular Formula: C9H11NO·HCl Molecular Weight: 185.65 MDL No.: MFCD08457629 Appearance: White powder Storage Temperature: Store at 0-8 °C

Purity Limit: &ge 98% (HPLC) CAS No.: 210488-55-4 Molecular Formula: C9H11NO·HCl Molecular Weight: 185.65 MDL No.: MFCD08457629 Appearance: White powder Storage Temperature: Store at 0-8 °C

Purity Limit: &ge 98% (HPLC) CAS No.: 210488-55-4 Molecular Formula: C9H11NO·HCl Molecular Weight: 185.65 MDL No.: MFCD08457629 Appearance: White powder Storage Temperature: Store at 0-8 °C

Purity Limit: &ge 98% (HPLC) CAS No.: 210488-55-4 Molecular Formula: C9H11NO·HCl Molecular Weight: 185.65 MDL No.: MFCD08457629 Appearance: White powder Storage Temperature: Store at 0-8 °C

A second-generation analog of (R)-roscovitine that inhibits Cdk1, 2, 5, and 9 (IC₅₀s = 0.09, 0.

A second-generation analog of (R)-roscovitine that inhibits Cdk1, 2, 5, and 9 (IC₅₀s = 0.09, 0.

An ER agonist that binds to ER&alpha and ER&beta with Ki values of 27.4 and 15.4 nM, respectively demonstrates higher ER agonist activity at ER&alpha compared to ER&beta (EC50 = 66 and 330 nM, respectively).