CID 76373319

Details

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Internal ID 5f933126-6454-478c-b65d-fc081071f479
Taxonomy Benzenoids > Phenols > 1-hydroxy-4-unsubstituted benzenoids
IUPAC Name
SMILES (Canonical) CC1C2(C=CC3=C(CO2)C(=CC=C3)O)OC(C4(O1)C=CC5=C(CO4)C(=CC=C5)O)C
SMILES (Isomeric) CC1C2(C=CC3=C(CO2)C(=CC=C3)O)OC(C4(O1)C=CC5=C(CO4)C(=CC=C5)O)C
InChI InChI=1S/C24H24O6/c1-15-23(11-9-17-5-3-7-21(25)19(17)13-27-23)30-16(2)24(29-15)12-10-18-6-4-8-22(26)20(18)14-28-24/h3-12,15-16,25-26H,13-14H2,1-2H3
InChI Key GWADQOOKXMSEMY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H24O6
Molecular Weight 408.40 g/mol
Exact Mass 408.15728848 g/mol
Topological Polar Surface Area (TPSA) 77.40 Ų
XlogP 3.20
Atomic LogP (AlogP) 4.10
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 76373319

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8847 88.47%
Caco-2 + 0.5558 55.58%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.6342 63.42%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9518 95.18%
OATP1B3 inhibitior + 0.9331 93.31%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6768 67.68%
P-glycoprotein inhibitior + 0.6931 69.31%
P-glycoprotein substrate - 0.7476 74.76%
CYP3A4 substrate + 0.5252 52.52%
CYP2C9 substrate + 0.5757 57.57%
CYP2D6 substrate - 0.7739 77.39%
CYP3A4 inhibition - 0.8942 89.42%
CYP2C9 inhibition - 0.7285 72.85%
CYP2C19 inhibition - 0.5977 59.77%
CYP2D6 inhibition - 0.8749 87.49%
CYP1A2 inhibition - 0.7067 70.67%
CYP2C8 inhibition - 0.7753 77.53%
CYP inhibitory promiscuity - 0.7168 71.68%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6047 60.47%
Eye corrosion - 0.9882 98.82%
Eye irritation - 0.7787 77.87%
Skin irritation - 0.7652 76.52%
Skin corrosion - 0.9443 94.43%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8279 82.79%
Micronuclear + 0.6800 68.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.7614 76.14%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.5671 56.71%
Acute Oral Toxicity (c) III 0.4538 45.38%
Estrogen receptor binding + 0.9519 95.19%
Androgen receptor binding + 0.6962 69.62%
Thyroid receptor binding + 0.7443 74.43%
Glucocorticoid receptor binding + 0.8405 84.05%
Aromatase binding + 0.7011 70.11%
PPAR gamma + 0.7168 71.68%
Honey bee toxicity - 0.9660 96.60%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9414 94.14%

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
CHEMBL1951 P21397 Monoamine oxidase A 99.17% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.33% 91.11%
CHEMBL240 Q12809 HERG 97.66% 89.76%
CHEMBL1937 Q92769 Histone deacetylase 2 90.13% 94.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.87% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.09% 95.56%
CHEMBL2581 P07339 Cathepsin D 87.28% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.89% 99.23%
CHEMBL2996 Q05655 Protein kinase C delta 83.80% 97.79%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.67% 86.33%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.86% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 82.32% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.90% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.55% 100.00%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 81.31% 85.11%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.17% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 80.59% 94.73%
CHEMBL1841 P06241 Tyrosine-protein kinase FYN 80.11% 81.29%

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 76373319
LOTUS LTS0032053
wikiData Q104167533