Phomolide E

Details

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Internal ID b7579e11-f0cd-4b83-b061-cd00999ff3ae
Taxonomy Organoheterocyclic compounds > Oxocins
IUPAC Name (2S,4S,5S,6E,8Z)-4,5-dihydroxy-2-(1-hydroxypropyl)-2,3,4,5-tetrahydrooxecin-10-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H18O5/c1-2-8(13)11-7-10(15)9(14)5-3-4-6-12(16)17-11/h3-6,8-11,13-15H,2,7H2,1H3/b5-3+,6-4-/t8?,9-,10-,11-/m0/s1
InChI Key CCFGKQCUMWRNLA-PRTGLMMUSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C12H18O5
Molecular Weight 242.27 g/mol
Exact Mass 242.11542367 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 0.40

Synonyms

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(2S,4S,5S,6E,8Z)-4,5-dihydroxy-2-(1-hydroxypropyl)-2,3,4,5-tetrahydrooxecin-10-one
RefChem:173337
CHEBI:220343

2D Structure

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2D Structure of Phomolide E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
No predicted properties yet!

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.15% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.82% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.26% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.35% 97.09%
CHEMBL2581 P07339 Cathepsin D 89.99% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.16% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.54% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.63% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.14% 86.33%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

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PubChem 139588837
LOTUS LTS0073989
wikiData Q104953227