Home Page Flashcards Roxatidine acetate hydrochloride C19H29ClN2O4 structure - Flashcards

Roxatidine acetate hydrochloride C19H29ClN2O4 structure – Flashcards

Flashcard maker : Robert Carter

Contents

Experimental Melting Point:
Experimental Solubility:
Target Organs:
Bio Activity:

Molecular Formula	C₁₉H₂₉ClN₂O₄
Average mass	384.898 Da
Density
Boiling Point
Flash Point
Molar Refractivity
Polarizability
Surface Tension
Molar Volume

Experimental data
Predicted – ACD/Labs
Predicted – ChemAxon

Experimental Physico-chemical Properties
- Experimental Melting Point:
  
  146 °C LKT Labs
  [R5894]
  
  147-149 °C LabNetwork LN01304839
- Experimental Solubility:
  
  DMSO 78 mg/mL; Water 77 mg/mL MedChem Express HY-B0305A
  
  DMSO:38mg/mL MedChem Express HY-B0305A

Miscellaneous

Target Organs:

Histamine Receptor antagonist TargetMol T0157

Bio Activity:

GPCR/G protein MedChem Express HY-B0305A

GPCR/G protein; Immunology/Inflammation; MedChem Express HY-B0305A

Histamine H2 receptor TargetMol T0157

Histamine Receptor MedChem Express HY-B0305A

Neuroscience TargetMol T0157

Roxatidine Acetate HCl is a specific and competitive histamin H2 receptor antagonist. MedChem Express

Roxatidine Acetate HCl is a specific and competitive histamin H2 receptor antagonist.; Target: Histamin H2 Receptor; Roxatidine acetate is a histamine H2-receptor antagonist which, after almost complete oral absorption (greater than 95%), is rapidly converted to its active metabolite, roxatidine, by esterases in the small intestine, plasma and liver. MedChem Express HY-B0305A

Roxatidine Acetate HCl is a specific and competitive histamin H2 receptor antagonist.;Target: Histamin H2 ReceptorRoxatidine acetate is a histamine H2-receptor antagonist which, after almost complete oral absorption (greater than 95%), is rapidly converted to its active metabolite, roxatidine, by esterases in the small intestine, plasma and liver. Roxatidine is a potent inhibitor of basal and stimulated gastric acid secretion in animals and humans and, like most other H2-receptor antagonists, has no anti-androgenic effects and does not interfere with the hepatic metabolism of other drugs [1, 2]. MedChem Express HY-B0305A

Predicted data is generated using the ACD/Labs Percepta Platform – PhysChem Module

No predicted properties have been calculated for this compound.

Density:
Boiling Point:
Vapour Pressure:
Enthalpy of Vaporization:
Flash Point:
Index of Refraction:
Molar Refractivity:
#H bond acceptors:
#H bond donors:
#Freely Rotating Bonds:
#Rule of 5 Violations:

ACD/LogP:
ACD/LogD (pH 5.5):
ACD/BCF (pH 5.5):
ACD/KOC (pH 5.5):
ACD/LogD (pH 7.4):
ACD/BCF (pH 7.4):
ACD/KOC (pH 7.4):
Polar Surface Area:
Polarizability:
Surface Tension:
Molar Volume:

Click to predict properties on the Chemicalize site

Roxatidine acetate hydrochloride C19H29ClN2O4 structure – Flashcards

Experimental Melting Point:

Experimental Solubility:

Target Organs:

Bio Activity:

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