Structure Database (LMSD)
Common Name
3a,16a-Dihydroxyandrostenone
Systematic Name
Synonyms
LM ID
LMST02020090
Formula
Exact Mass
Calculate m/z
304.203845
Sum Composition
Status
Active
3D model of 3a,16a-Dihydroxyandrostenone
Please note: Where there are chiral atoms but the stereochemistry is undefined, the 3D model takes an arbitrary conformation
Classification
Category
Main Class
Sub Class
String Representations
InChiKey (Click to copy)
QQIVKFZWLZJXJT-ZLOBMTTQSA-N
InChi (Click to copy)
InChI=1S/C19H28O3/c1-18-7-5-12(20)9-11(18)3-4-13-14(18)6-8-19(2)15(13)10-16(21)17(19)22/h3,12-16,20-21H,4-10H2,1-2H3/t12-,13-,14+,15+,16-,18+,19+/m1/s1
SMILES (Click to copy)
[C@@]12([H])CC=C3C[C@H](O)CC[C@]3(C)[C@@]1([H])CC[C@]1(C)C(=O)[C@H](O)C[C@@]21[H]
Other Databases
Calculated Physicochemical Properties
Heavy Atoms
22
Rings
4
Aromatic Rings
0
Rotatable Bonds
0
Van der Waals Molecular Volume
308.91
Topological Polar Surface Area
57.53
Hydrogen Bond Donors
2
Hydrogen Bond Acceptors
3
logP
3.42
Molar Refractivity
85.13
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Created at
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Updated at
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