SCS-C007194
24,24,26,26-tetramethylcholesta-5,25(29)-dien-3β-ol
Pathway: Terpenoids
Superclass: Steroids
Class: Cholestane steroids | Ergostane steroids
Chemical Structure
Loading 3D structure...
3D conformers are computationally generated from SMILES by RDKit for visualization and download; they are not experimental crystal or NMR structures.
Source Information
Halichondria sp.
(NA)
Kingdom
Metazoa
Phylum
Porifera
Class
Demospongiae
Order
Suberitida
Family
Halichondriidae
Genus
Halichondria
Species
Halichondria sp.
Offshore Hainan Island
· 18°13′56″ N, 109°21′38″ E
DOI:
10.1016/j.fitote.2021.104918
· Fitoterapia
Drug-likeness (Lipinski Ro5)
Molecular Weight
440.8 Da
Threshold ≤ 500
ALogP
8.58
Threshold ≤ 5
H-Bond Donors
1
Threshold ≤ 5
H-Bond Acceptors
1
Threshold ≤ 10
1 violation (ALogP) — borderline drug-like
Chemical Properties
Molecular Formula:
C31H52O
Molecular Weight:
440.7560 Da
SMILES:
C=C(C(C)C)C(C)(C)CC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
InChIKey:
DTJUZPVJJRFCAZ-ANSWHRQLSA-N
InChI:
InChI=1S/C31H52O/c1-20(2)22(4)29(5,6)16-13-21(3)26-11-12-27-25-10-9-23-19-24(32)14-17-30(23,7)28(25)15-18-31(26,27)8/h9,20-21,24-28,32H,4,10-19H2,1-3,5-8H3/t21-,24+,25+,26-,27+,28+,30+,31-/m1/s1
Calculated Properties
ALogP:
8.581 lipophilicity
TPSA:
20.23 Ų polar surface area
H-Bond Donors:
1
H-Bond Acceptors:
1
Rotatable Bonds:
6
Ring Count:
4
(0 aromatic)
Chiral Centers:
8
Fsp³:
0.8710 fraction sp³ carbon
Database Information
Compound ID:
SCS-C007194
NPClassifier Pathway:
Terpenoids
NPClassifier Superclass:
Steroids
NPClassifier Class:
Cholestane steroids
Ergostane steroids
Glycoside:
No
NPClassifier Status:
Classified
External Links:
General chemistry
Natural product databases
Biological Activity Data
No bioactivity data available for this compound.