Larsucosterol

This drug entry is a stub and has not been fully annotated. It is scheduled to be annotated soon.

Identification

Generic Name
Larsucosterol
DrugBank Accession Number
DB18079
Background

Not Available

Type
Small Molecule
Groups
Investigational
Structure
Weight
Average: 482.72
Monoisotopic: 482.306595755
Chemical Formula
C27H46O5S
Synonyms
  • 25-hydroxycholest-5-en-3.beta.-yl hydrogen sulfate
  • 5-cholesten-3.beta.-25-diol-3-sulfate
  • 5-cholesten-3.beta., 25-diol 3-sulfate
  • Cholest-5-ene-3,25-diol, 3-(hydrogen sulfate), (3.beta.)-
External IDs
  • 25HC3S
  • DUR-928
  • DV-928

Pharmacology

Indication

Not Available

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Contraindications & Blackbox Warnings
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Pharmacodynamics

Not Available

Mechanism of action
Not Available
Absorption

Not Available

Volume of distribution

Not Available

Protein binding

Not Available

Metabolism
Not Available
Route of elimination

Not Available

Half-life

Not Available

Clearance

Not Available

Adverse Effects
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Toxicity

Not Available

Pathways
Not Available
Pharmacogenomic Effects/ADRs
Not Available

Interactions

Drug Interactions
This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist.
Not Available
Food Interactions
Not Available

Products

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Product Ingredients
IngredientUNIICASInChI Key
Larsucosterol sodium71A5JOPBE81174047-40-5OEGAOHNRCSZIRO-KSGNISEOSA-M

Categories

Drug Categories
Classification
Not classified
Affected organisms
Not Available

Chemical Identifiers

UNII
UGX2V7MGMZ
CAS number
884905-07-1
InChI Key
PIUZYOCNZPYXOA-ZHHJOTBYSA-N
InChI
InChI=1S/C27H46O5S/c1-18(7-6-14-25(2,3)28)22-10-11-23-21-9-8-19-17-20(32-33(29,30)31)12-15-26(19,4)24(21)13-16-27(22,23)5/h8,18,20-24,28H,6-7,9-17H2,1-5H3,(H,29,30,31)/t18-,20+,21-,22-,23-,24-,26+,27+/m1/s1
IUPAC Name
[(1R,3aS,3bS,7S,9aR,9bS,11aR)-1-[(2R)-6-hydroxy-6-methylheptan-2-yl]-9a,11a-dimethyl-1H,2H,3H,3aH,3bH,4H,6H,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-7-yl]oxidanesulfonic acid
SMILES
[H][C@@]1(CC[C@@]2([H])[C@]3([H])CC=C4C[C@H](CC[C@]4(C)[C@@]3([H])CC[C@]12C)OS(O)(=O)=O)[C@H](C)CCCC(C)(C)O

References

General References
Not Available
ChemSpider
9758645
ChEMBL
CHEMBL4802158

Clinical Trials

Clinical Trials
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PhaseStatusPurposeConditionsCountStart DateWhy Stopped100+ additional columns
2CompletedTreatmentAlcoholic Hepatitis (AH)3somestatusstop reasonjust information to hide
2CompletedTreatmentPsoriasis Vulgaris (Plaque Psoriasis)1somestatusstop reasonjust information to hide
2TerminatedTreatmentCoronavirus Disease 2019 (COVID‑19)1somestatusstop reasonjust information to hide
2TerminatedTreatmentPrimary Sclerosing Cholangitis (PSC)1somestatusstop reasonjust information to hide

Pharmacoeconomics

Manufacturers
Not Available
Packagers
Not Available
Dosage Forms
Not Available
Prices
Not Available
Patents
Not Available

Properties

State
Not Available
Experimental Properties
Not Available
Predicted Properties
PropertyValueSource
logP4.33Chemaxon
pKa (Strongest Acidic)-1.6Chemaxon
pKa (Strongest Basic)-1Chemaxon
Physiological Charge-1Chemaxon
Hydrogen Acceptor Count4Chemaxon
Hydrogen Donor Count2Chemaxon
Polar Surface Area83.83 Å2Chemaxon
Rotatable Bond Count7Chemaxon
Refractivity132.44 m3·mol-1Chemaxon
Polarizability57.38 Å3Chemaxon
Number of Rings4Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterNoChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleYesChemaxon
Predicted ADMET Features
Not Available

Spectra

Mass Spec (NIST)
Not Available
Spectra
Not Available
Chromatographic Properties
Collision Cross Sections (CCS)
Not Available

Drug created at September 09, 2023 01:24 / Updated at September 28, 2023 05:48