SCS-C007196

7,22,25-trienergosta-3β,5α,6β,9α-tetraol

Pathway: Terpenoids Superclass: Steroids Class: Cholestane steroids

Chemical Structure

Structure of 7,22,25-trienergosta-3β,5α,6β,9α-tetraol
Loading 3D structure...
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

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
444.7 Da
Threshold ≤ 500
ALogP
4.53
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:
C28H44O4
Molecular Weight:
444.6560 Da
SMILES:
C=C(C)[C@H](C)/C=C/C(C)C1CCC2C3=C[C@@H](O)[C@@]4(O)C[C@@H](O)CC[C@]4(C)[C@@]3(O)CC[C@@]21C
InChIKey:
CUCXDHFOOHLHGH-VDUVICEZSA-N
InChI:
InChI=1S/C28H44O4/c1-17(2)18(3)7-8-19(4)21-9-10-22-23-15-24(30)28(32)16-20(29)11-12-26(28,6)27(23,31)14-13-25(21,22)5/h7-8,15,18-22,24,29-32H,1,9-14,16H2,2-6H3/b8-7+/t18-,19?,20+,21?,22?,24-,25-,26-,27-,28+/m1/s1
Calculated Properties
ALogP:
4.531 lipophilicity
TPSA:
80.92 Ų polar surface area
H-Bond Donors:
4
H-Bond Acceptors:
4
Rotatable Bonds:
4
Ring Count:
4 (0 aromatic)
Chiral Centers:
10
Fsp³:
0.7857 fraction sp³ carbon

Database Information

Compound ID:
SCS-C007196
NPClassifier Pathway:
Terpenoids
NPClassifier Superclass:
Steroids
NPClassifier Class:
Cholestane steroids
Glycoside:
No
NPClassifier Status:
Classified
External Links:

Biological Activity Data

Activity values are displayed only when a quantitative or clearly reported result is available. Tested organisms, cell lines and molecular targets are shown under Target / model.
Activity Assay Target / model Result Reference
Enzyme inhibition — human protein tyrosine phosphatase 1B (PTP1B) All the isolates were subjected for various bioassays, such as human protein tyrosine phosphatase 1B (PTP1B) enzyme inhibitory and cytotoxicity against HT-29, SNU-398, and Capan-1 cells, etc. However, none of them showed positive effects. 10.1016/j.fitote.2021.104918 Fitoterapia
Antitumor — PTP1B All the isolates were subjected for various bioassays, such as human protein tyrosine phosphatase 1B (PTP1B) enzyme inhibitory and cytotoxicity against HT-29, SNU-398, and Capan-1 cells, etc. However, none of them showed positive effects. 10.1016/j.fitote.2021.104918 Fitoterapia
Structure enlarged