FB2024_03 , released June 25, 2024
Chemical: jaspamide
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General Information
Name
jaspamide
FlyBase ID
FBch0001739
ChEBI Name
jaspamide
ChEBI ID
PubChem Name
Jasplakinolide
PubChem ID
9831636 (PubChem link: Jasplakinolide)
Chemical Structure
Chemical structure of jaspamide
jaspamide
InChIKey

GQWYWHOHRVVHAP-DHKPLNAMSA-N

Definition (ChEBI)

A cyclodepsipeptide isolated from Jaspis splendens and has been shown to exhibit antineoplastic activity. It is an actin polymerization and stabilization inducer.

Roles Classification (ChEBI)
Comment
Synonyms and Secondary IDs (22)
Synonyms
(+)-Jasplakinolide
(4R,7R,10S,13S,15E,17R,19S)-7-[(2-Bromo-1H-indol-3-yl)methyl]-4-(4-hydroxyphenyl)-8,10,13,15,17,19-hexamethyl-1-oxa-5,8,11-triazacyclononadec-15-ene-2,6,9,12-tetrone
(4r,7r,10s,13s,15e,17r,19s)-7-[(2-bromo-1h-indol-3-yl)methyl]-4-(4-hydroxyphenyl)-8,10,13,15,17,19-hexamethyl-1-oxa-5,8,11-triazacyclononadec-15-ene-2,6,9,12-tetrone
102396-24-7
C36H45BrN4O6
CHEBI:66104
Jaspamide
Jasplakinolide
MLS002702908
NSC613009
PubChem:9831636
SCHEMBL62754
beta-Alanine, N-(2-bromo-N-(N-(8-hydroxy-2,4,6-trimethyl-1-oxo-4-nonenyl)-L-alanyl)-N-methyl-D-tryptophyl)-L-3-(4-hydroxyphenyl)-, p-lactone, (2S-(2R*,4E,6S*,8R*))-
beta-alanine, n-(2-bromo-n-(n-(8-hydroxy-2,4,6-trimethyl-1-oxo-4-nonenyl)-l-alanyl)-n-methyl-d-tryptophyl)-l-3-(4-hydroxyphenyl)-, p-lactone, (2s-(2r*,4e,6s*,8r*))-
c36h45brn4o6
chebi:66104
mls002702908
nsc613009
pubchem:9831636
schembl62754
Secondary FlyBase IDs
    References (6)