Structure Database (LMSD)

Common Name
Glisoprenin E
Systematic Name
3,7,11,15,19,23,27,31,35-nonamethylhexatriaconta-2E,10E,14E-triene-1,6,7,19,23,27,31,34,35-nonol
Synonyms
LM ID
LMPR01080069
Formula
Exact Mass
Calculate m/z
770.627185
Status
Curated

Classification

References

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Clonostachys rosea (#29856)
Sordariomycetes (#147550)
Glisoprenins C, D and E, new inhibitors of appressorium formation in Magnaporthe grisea, from cultures of Gliocladium roseum. 2. Structure determination.,
J Antibiot (Tokyo), 1998
Pubmed ID: 9544946

String Representations

InChiKey (Click to copy)
FXTQBFBSROLPRX-FHAYICFZSA-N
InChi (Click to copy)
InChI=1S/C45H86O9/c1-35(17-11-18-36(2)20-13-32-45(10,54)39(48)22-21-37(3)24-34-46)19-12-25-41(6,50)26-14-27-42(7,51)28-15-29-43(8,52)30-16-31-44(9,53)33-23-38(47)40(4,5)49/h17,20,24,38-39,46-54H,11-16,18-19,21-23,25-34H2,1-10H3/b35-17+,36-20+,37-24+
SMILES (Click to copy)
C(/C=C(\C)/CCC(O)C(O)(C)CC/C=C(\C)/CC/C=C(\C)/CCCC(O)(C)CCCC(C)(O)CCCC(C)(O)CCCC(O)(CCC(O)C(O)(C)C)C)O

Other Databases

PubChem CID

Calculated Physicochemical Properties

Heavy Atoms 54
Rings
Aromatic Rings
Rotatable Bonds 31
Van der Waals Molecular Volume 858.25
Topological Polar Surface Area 182.07
Hydrogen Bond Donors 9
Hydrogen Bond Acceptors 9
logP 10.44
Molar Refractivity 226.71

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Created at
6th Mar 2024
Updated at
6th Mar 2024