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Molecule
ID:133095
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₂₁H₃₆O₃
Molecular Mass
336.50874
Exact Mass
336.26644501
Charge
0
InChI
InChI=1S/C21H36O3/c1-13(22)21(24)11-8-18-16-5-4-14-12-15(23)6-9-19(14,2)17(16)7-10-20(18,21)3/h13-18,22-24H,4-12H2,1-3H3/t13-,14+,15-,16-,17+,18+,19+,20+,21+/m1/s1
InChIKey
SCPADBBISMMJAW-MUHHAPIYSA-N
Canonic Smiles
O[C@@H]1CC[C@]2([C@H](C1)CC[C@@H]1[C@@H]2CC[C@]2([C@H]1CC[C@]2(O)[C@H](O)C)C)C
Isomeric Smiles
C[C@H]([C@]1(CC[C@@H]2[C@@]1(CC[C@H]1[C@H]2CC[C@@H]2[C@@]1(CC[C@H](C2)O)C)C)O)O
Calculated Properties
JChem
Acid pKa
13.417381
H Acceptors
3
H Donor
3
LogD (pH = 5.5)
2.8539984
LogD (pH = 7.4)
2.8539982
Log P
2.8539987
Molar Refractivity
95.2319
Polarizability
38.348473
Polar Surface Area
60.69
Rotatable Bonds
1
Lipinski's Rule of Five
true
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Related Proteins
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
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RDKit
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Synonyms
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IUPAC Traditional name
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IUPAC name
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EC Number
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CAS Number
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PubChem CID
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PubChem SID
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Sigma Aldrich
P2507
Academic Data
PubChem
21116119
Names and Identifiers
Synonyms
5α-孕烷-3α,17α,20β-三醇
别孕烷-3α,17α,20β-三醇
3α,17α,20β-三羟基-5α-孕烷
5α-Pregnane-3α,17α,20β-triol
IUPAC Traditional name
(1S,2S,5R,7S,10R,11S,14R,15S)-14-[(1R)-1-hydroxyethyl]-2,15-dimethyltetracyclo[8.7.0.0
2
,
7
.0
1
1
,
1
5
]heptadecane-5,14-diol
IUPAC name
(1S,2S,5R,7S,10R,11S,14R,15S)-14-[(1R)-1-hydroxyethyl]-2,15-dimethyltetracyclo[8.7.0.0
2
,
7
.0
1
1
,
1
5
]heptadecane-5,14-diol
Registration numbers
EC Number
237-708-6
CAS Number
13933-75-0
PubChem CID
21116119
PubChem SID
162227372
Properties
Safety Information
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
German water hazard class
3
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay