Irlactin G

Details

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Internal ID 2a17fd97-bd43-4565-a63c-e05948f82781
Taxonomy Organoheterocyclic compounds > Tetrahydrofurans
IUPAC Name (1R,7S,8R,9S,11R)-11-methoxy-5,5,8-trimethyl-10-oxatricyclo[7.2.1.03,7]dodec-2-ene-2-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H24O3/c1-9-11-6-16(2,3)7-12(11)13(8-17)10-5-14(9)19-15(10)18-4/h8-11,14-15H,5-7H2,1-4H3/t9-,10-,11+,14+,15-/m1/s1
InChI Key FRNTWFACHLMROJ-HFLGISGGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H24O3
Molecular Weight 264.36 g/mol
Exact Mass 264.17254462 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 2.30

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Irlactin G

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 97.09% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.23% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.22% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.86% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.85% 91.11%
CHEMBL226 P30542 Adenosine A1 receptor 87.87% 95.93%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 87.25% 86.92%
CHEMBL3401 O75469 Pregnane X receptor 82.55% 94.73%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.29% 100.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.23% 97.14%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.70% 85.14%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 146684317
LOTUS LTS0128271
wikiData Q105000319