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Molecule
ID:127282
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₂₈H₄₄O
Molecular Mass
396.64836
Exact Mass
396.33921603
Charge
0
InChI
InChI=1S/C28H44O/c1-19(2)20(3)9-10-22(5)26-15-16-27-23(8-7-17-28(26,27)6)12-13-24-18-25(29)14-11-21(24)4/h9-10,12-13,19-20,22,25-27,29H,4,7-8,11,14-18H2,1-3,5-6H3/t20-,22+,25-,26+,27-,28+/m0/s1
InChIKey
MECHNRXZTMCUDQ-FWTXJDITSA-N
Canonic Smiles
O[C@H]1CCC(=C)/C(=C/C=C\2/CCC[C@]3([C@H]2CC[C@@H]3[C@@H](C=C[C@@H](C(C)C)C)C)C)/C1
Isomeric Smiles
O[C@@H]1C/C(=C\C=C/2\CCC[C@]3([C@H]2CC[C@@H]3[C@@H](C=C[C@H](C)C(C)C)C)C)/C(=C)CC1
Calculated Properties
JChem
Acid pKa
18.384342
H Acceptors
1
H Donor
1
LogD (pH = 5.5)
7.050558
LogD (pH = 7.4)
7.050558
Log P
7.050558
Molar Refractivity
128.8897
Polarizability
49.86576
Polar Surface Area
20.23
Rotatable Bonds
5
Lipinski's Rule of Five
false
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Ergocalciferol
PubChem
71308193
Names and Identifiers
Synonyms
Drisdol (Sanofi-Synthelabo)
Calcidol (Patrin Pharma)
Ergocalciferol
IUPAC name
(1S)-3-{2-[(1R,3aS,7aR)-1-[(2R,5R)-5,6-dimethylhept-3-en-2-yl]-7a-methyl-octahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexan-1-ol
IUPAC Traditional name
(1S)-3-{2-[(1R,3aS,7aR)-1-[(2R,5R)-5,6-dimethylhept-3-en-2-yl]-7a-methyl-hexahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexan-1-ol
Registration numbers
PubChem CID
5280793
71308193
CHEMBL
1536
Unique Ingredient Identifier
VS041H42XC
CAS Number
50-14-6
CHEBI ID
28934
Wikipedia Title
Ergocalciferol
ATC CODE
A11CC01
DrugBank ID
DB00153
KEGG ID
C05441
Chemspider ID
4444351
PubChem SID
162221603
Properties
Physical Property
Melting Point
114–118 °C
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Ergocalciferol
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