Structure Database (LMSD)
Common Name
5beta-hydroxy-rubrosterone
Systematic Name
2β,3β,5β,14α-tetrahydroxy-androst-7-en-6,17-dione
Synonyms
LM ID
LMST02020146
Formula
Exact Mass
Calculate m/z
350.17294
Sum Composition
Status
Active
No other lipid differing only in stereochemistry/bond geometry found
3D model of 5beta-hydroxy-rubrosterone
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
References
String Representations
InChiKey (Click to copy)
OEJRYBSXPXGVNX-LWZFRQFWSA-N
InChi (Click to copy)
InChI=1S/C19H26O6/c1-16-5-3-10-11(18(16,24)6-4-14(16)22)7-15(23)19(25)9-13(21)12(20)8-17(10,19)2/h7,10,12-13,20-21,24-25H,3-6,8-9H2,1-2H3/t10-,12-,13+,16+,17+,18+,19+/m0/s1
SMILES (Click to copy)
O[C@@H]1C[C@@]2([C@@]([C@]3([H])C([C@]4([C@](CC3)(C(CC4)=O)C)O)=CC2=O)(C[C@@H]1O)C)O
Other Databases
PubChem CID
Calculated Physicochemical Properties
Heavy Atoms
25
Rings
4
Aromatic Rings
Rotatable Bonds
Van der Waals Molecular Volume
332.64
Topological Polar Surface Area
115.06
Hydrogen Bond Donors
4
Hydrogen Bond Acceptors
6
logP
1.40
Molar Refractivity
89.46
Admin
Created at
10th Jan 2024
Updated at
10th Jan 2024