SCS-C003480

7α-hydroxy-crassarosterol A

Pathway: Terpenoids Superclass: Steroids Class: Ergostane steroids

Chemical Structure

Structure of 7α-hydroxy-crassarosterol A
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3D conformers are computationally generated from SMILES by RDKit for visualization and download; they are not experimental crystal or NMR structures.
Download: SDF SMILES

Source Information

Sinularia flexibilis (soft coral)
Kingdom Metazoa Phylum Cnidaria Class Anthozoa Order Malacalcyonacea Family Sinulariidae Genus Sinularia Species Sinularia flexibilis
Yalong Bay
DOI: 10.1016/j.steroids.2014.08.027  · Steroids

Drug-likeness (Lipinski Ro5)

Molecular Weight
446.7 Da
Threshold ≤ 500
ALogP
4.47
Threshold ≤ 5
H-Bond Donors
4
Threshold ≤ 5
H-Bond Acceptors
4
Threshold ≤ 10
Passes Lipinski Rule of Five — drug-like candidate

Chemical Properties

Molecular Formula:
C28H46O4
Molecular Weight:
446.6720 Da
SMILES:
C=C(CC[C@@H](C)[C@H]1[C@@H](O)C[C@H]2[C@H]3[C@H]([C@H](O)C[C@]12C)[C@@]1(C)CC[C@H](O)CC1=C[C@H]3O)C(C)C
InChIKey:
VVKLXTWRXYGASH-UDDROMQNSA-N
InChI:
InChI=1S/C28H46O4/c1-15(2)16(3)7-8-17(4)25-22(31)13-20-24-21(30)12-18-11-19(29)9-10-27(18,5)26(24)23(32)14-28(20,25)6/h12,15,17,19-26,29-32H,3,7-11,13-14H2,1-2,4-6H3/t17-,19+,20+,21-,22+,23-,24-,25+,26+,27+,28+/m1/s1
Calculated Properties
ALogP:
4.467 lipophilicity
TPSA:
80.92 Ų polar surface area
H-Bond Donors:
4
H-Bond Acceptors:
4
Rotatable Bonds:
5
Ring Count:
4 (0 aromatic)
Chiral Centers:
11
Fsp³:
0.8571 fraction sp³ carbon

Database Information

Compound ID:
SCS-C003480
NPClassifier Pathway:
Terpenoids
NPClassifier Superclass:
Steroids
NPClassifier Class:
Ergostane steroids
Glycoside:
No
NPClassifier Status:
Classified
External Links:

Biological Activity Data

No bioactivity data available for this compound.

Structure enlarged