CID 46882365

Details

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Internal ID a6c25409-e344-4cc7-9621-512b2a306a37
Taxonomy Organoheterocyclic compounds > Naphthofurans
IUPAC Name [(5aS,9aS,9bS)-9b-hydroxy-6,6,9a-trimethyl-1-oxo-3,5,5a,7,8,9-hexahydrobenzo[e][2]benzofuran-5-yl] (2E,4E,6E)-9-hydroxydeca-2,4,6-trienoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H34O6/c1-17(26)11-8-6-5-7-9-12-20(27)31-19-15-18-16-30-22(28)25(18,29)24(4)14-10-13-23(2,3)21(19)24/h5-9,12,15,17,19,21,26,29H,10-11,13-14,16H2,1-4H3/b7-5+,8-6+,12-9+/t17?,19?,21-,24-,25-/m0/s1
InChI Key ZHQUHDHFPDBIHU-HKJWLHPRSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C25H34O6
Molecular Weight 430.50 g/mol
Exact Mass 430.23553880 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.40
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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CHEMBL1080952

2D Structure

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2D Structure of CID 46882365

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9889 98.89%
Caco-2 - 0.6348 63.48%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.8640 86.40%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8426 84.26%
OATP1B3 inhibitior + 0.8822 88.22%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5646 56.46%
BSEP inhibitior + 0.7858 78.58%
P-glycoprotein inhibitior + 0.6454 64.54%
P-glycoprotein substrate - 0.6341 63.41%
CYP3A4 substrate + 0.6616 66.16%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9077 90.77%
CYP3A4 inhibition - 0.6965 69.65%
CYP2C9 inhibition - 0.6037 60.37%
CYP2C19 inhibition - 0.8882 88.82%
CYP2D6 inhibition - 0.9292 92.92%
CYP1A2 inhibition - 0.7759 77.59%
CYP2C8 inhibition + 0.4453 44.53%
CYP inhibitory promiscuity - 0.8250 82.50%
UGT catelyzed - 0.5638 56.38%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.4848 48.48%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.9700 97.00%
Skin irritation + 0.5969 59.69%
Skin corrosion - 0.9305 93.05%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4519 45.19%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.5541 55.41%
skin sensitisation - 0.8878 88.78%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.7927 79.27%
Acute Oral Toxicity (c) III 0.5183 51.83%
Estrogen receptor binding + 0.7086 70.86%
Androgen receptor binding + 0.7091 70.91%
Thyroid receptor binding + 0.5820 58.20%
Glucocorticoid receptor binding + 0.7129 71.29%
Aromatase binding + 0.6308 63.08%
PPAR gamma - 0.5921 59.21%
Honey bee toxicity - 0.8514 85.14%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9858 98.58%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.15% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.68% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.65% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.99% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.39% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.31% 98.95%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 90.34% 96.77%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.74% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.95% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.84% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.62% 85.14%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.86% 91.07%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.82% 92.62%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.07% 97.28%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.67% 95.71%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.30% 89.34%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.29% 100.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 80.13% 90.08%

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 46882365
LOTUS LTS0147667
wikiData Q105375961