Structure Database (LMSD)
Common Name
Cytochalasin H1
Systematic Name
Synonyms
3D model of Cytochalasin H1
Please note: Where there are chiral atoms but the stereochemistry is undefined, the 3D model takes an arbitrary conformation
Classification
References
Taxonomy Information
Curated from
NCBI taxonomy class
Reference
Phomopsis sp.
(#1715245)
Sordariomycetes
(#147550)
Cytochalasins from an Australian Marine Sediment-Derived Phomopsis sp. (CMB-M0042F): Acid-Mediated Intramolecular Cycloadditions Enhance Chemical Diversity.,
J Org Chem, 2017
J Org Chem, 2017
Pubmed ID:
28831797
String Representations
InChiKey (Click to copy)
WWRGSXNVSSJVGN-HGXVHBSISA-N
InChi (Click to copy)
InChI=1S/C31H41NO5/c1-19-11-10-14-24-28(34)21(3)20(2)27-25(17-23-12-8-7-9-13-23)32-29(35)31(24,27)26(37-22(4)33)15-16-30(5,18-19)36-6/h7-10,12-16,19-20,24-28,34H,3,11,17-18H2,1-2,4-6H3,(H,32,35)/b14-10+,16-15+/t19-,20+,24-,25-,26+,27-,28+,30-,31+/m0/s1
SMILES (Click to copy)
[C@@H]1(C)C(=C)[C@@H](O)[C@]2([H])C=CC[C@H](C)C[C@@](C)(OC)C=C[C@@H](OC(=O)C)[C@@]32C(=O)N[C@@H](CC2C=CC=CC=2)[C@]13[H]
Other Databases
PubChem CID
Calculated Physicochemical Properties
Heavy Atoms
37
Rings
4
Aromatic Rings
1
Rotatable Bonds
5
Van der Waals Molecular Volume
518.35
Topological Polar Surface Area
84.86
Hydrogen Bond Donors
2
Hydrogen Bond Acceptors
6
logP
5.54
Molar Refractivity
145.49
Admin
Created at
28th Jul 2020
Updated at
2nd Apr 2024