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Home CSSS02515436635

Structure Info


Chemspace ID
CSSS02515436635 (In-Stock Screening Compounds)
IUPAC Name
sodium (4R)-4-[(1R,3aS,3bR,5aS,9aS,9bS,11aR)-9a,11a-dimethyl-4,7,11-trioxo-hexadecahydro-1H-cyclopenta[a]phenanthren-1-yl]pentanoate
Mol formula
C24H33NaO5
Mol weight
425 Da
Catalog Number(s)
HY-B0998, S083923

Properties

LogP
4.77
Heavy atoms count
30
Rotatable bond count
5
Number of rings
4
Carbon bond saturation, Fsp3
0.833
Polar surface area (Å)
78
Hydrogen bond acceptors count
4
Hydrogen bond donors count
0

SDS

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Items Overall 6 items from 2 suppliers

SupplierLead timeShips fromPurityPackPrice, $Qty
MedChemExpress10 daysUnited States
To:
98500 mg75
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MedChemExpress10 daysUnited States
To:
985 g250
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MedChemExpress10 daysUnited States
To:
9810mM/1mL83
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Description: Names: Dehydrocholate (sodium); Sodium dehydrocholate; Product Description: Dehydrocholic sodium is a hydrocholeretic, increasing bile output to clear increased bile acid load.; Target: Endogenous Metabolite; CAS: 145-41-5
MedChemExpress EU10 daysSweden
To:
98500 mg79
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MedChemExpress EU10 daysSweden
To:
985 g263
Go to cartEnquire
MedChemExpress EU10 daysSweden
To:
9810mM/1mL88
Go to cartEnquire
Description: Names: Dehydrocholate (sodium); Sodium dehydrocholate; Product Description: Dehydrocholate sodium is an orally active hydrocholeretic agent. Dehydrocholate sodium modulates Autophagy, reduces serum amylase and lipase levels. Dehydrocholate sodium has the effects of promoting choleretic function, protecting the liver, reducing pancreatic damage, and regulating cholesterol metabolism. Dehydrocholate sodium can be used in the study of acute biliary pancreatitis and obstructive jaundice; Target: Amylases;Autophagy;Lipase; CAS: 145-41-5
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