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Molecule
ID:132066
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₂₁H₃₆O₂
Molecular Mass
320.50934
Exact Mass
320.27153039
Charge
0
InChI
InChI=1S/C21H36O2/c1-13(22)17-6-7-18-16-5-4-14-12-15(23)8-10-20(14,2)19(16)9-11-21(17,18)3/h13-19,22-23H,4-12H2,1-3H3/t13-,14+,15-,16-,17+,18-,19-,20-,21+/m0/s1
InChIKey
YWYQTGBBEZQBGO-HUTKLZKUSA-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@@H]2[C@@H](O)C)C)C
Isomeric Smiles
C[C@@H]([C@H]1CC[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
Calculated Properties
JChem
Acid pKa
18.296396
H Acceptors
2
H Donor
2
LogD (pH = 5.5)
3.779437
LogD (pH = 7.4)
3.779437
Log P
3.779437
Molar Refractivity
93.9348
Polarizability
37.734753
Polar Surface Area
40.46
Rotatable Bonds
1
Lipinski's Rule of Five
true
Data Source
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Properties
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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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IUPAC Traditional name
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IUPAC name
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PubChem CID
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PubChem SID
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From Data Sources
Bioactivity
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Data Source
Commercial Catalog
Sigma Aldrich
P7004
Academic Data
PubChem
57358762
Names and Identifiers
Synonyms
5β-Pregnane-3β,20α-diol
3β,20α-Dihydroxy-5β-pregnane
IUPAC Traditional name
(1S,2S,5S,7R,10R,11S,14S,15S)-14-[(1S)-1-hydroxyethyl]-2,15-dimethyltetracyclo[8.7.0.0
2
,
7
.0
1
1
,
1
5
]heptadecan-5-ol
IUPAC name
(1S,2S,5S,7R,10R,11S,14S,15S)-14-[(1S)-1-hydroxyethyl]-2,15-dimethyltetracyclo[8.7.0.0
2
,
7
.0
1
1
,
1
5
]heptadecan-5-ol
Registration numbers
CAS Number
80-90-0
PubChem CID
57358762
PubChem SID
162226343
Properties
Safety Information
German water hazard class
3
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay