3,4-Dehydrolarreatricin

Details

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Internal ID 20eebee4-06b9-4afa-94a8-4477a3fac124
Taxonomy Benzenoids > Phenols > 1-hydroxy-2-unsubstituted benzenoids
IUPAC Name 4-[(2R,5R)-5-(4-hydroxyphenyl)-3,4-dimethyl-2,5-dihydrofuran-2-yl]phenol
SMILES (Canonical) CC1=C(C(OC1C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C
SMILES (Isomeric) CC1=C([C@H](O[C@@H]1C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C
InChI InChI=1S/C18H18O3/c1-11-12(2)18(14-5-9-16(20)10-6-14)21-17(11)13-3-7-15(19)8-4-13/h3-10,17-20H,1-2H3/t17-,18-/m0/s1
InChI Key QLSUUELDMMCCEI-ROUUACIJSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H18O3
Molecular Weight 282.30 g/mol
Exact Mass 282.125594432 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 2.80

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,4-Dehydrolarreatricin

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
CHEMBL3401 O75469 Pregnane X receptor 89.57% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.77% 91.11%
CHEMBL242 Q92731 Estrogen receptor beta 86.97% 98.35%
CHEMBL1951 P21397 Monoamine oxidase A 86.95% 91.49%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 86.48% 90.93%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.02% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.77% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.44% 97.09%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 81.69% 85.00%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 81.47% 93.10%
CHEMBL2581 P07339 Cathepsin D 81.17% 98.95%

Plants that contains it

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Cross-Links

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PubChem 25775479
NPASS NPC136531