CID 163187817

Details

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Internal ID 61c83e30-c33a-41d0-bd34-0f846382226c
Taxonomy Organoheterocyclic compounds > Oxepanes
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C45H82N6O5/c1-3-38-24-16-17-28-44(56-38)35-37-26-27-39-41(45(29-21-23-36(2)55-45)49-43(48-44)51(37)39)42(53)54-34-20-14-12-10-8-6-4-5-7-9-11-13-15-25-40(52)50(33-22-31-47)32-19-18-30-46/h36-39,41H,3-35,46-47H2,1-2H3,(H,48,49)/t36-,37+,38+,39-,41-,44+,45-/m1/s1
InChI Key XCQKBLKCMOARAT-COYUCOOOSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C45H82N6O5
Molecular Weight 787.20 g/mol
Exact Mass 786.63466974 g/mol
Topological Polar Surface Area (TPSA) 145.00 Ų
XlogP 8.00
Atomic LogP (AlogP) 8.07
H-Bond Acceptor 10
H-Bond Donor 3
Rotatable Bonds 25

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 163187817

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9425 94.25%
Caco-2 - 0.8439 84.39%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Lysosomes 0.7553 75.53%
OATP2B1 inhibitior - 0.5688 56.88%
OATP1B1 inhibitior + 0.8474 84.74%
OATP1B3 inhibitior + 0.9397 93.97%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.9473 94.73%
P-glycoprotein inhibitior + 0.7330 73.30%
P-glycoprotein substrate + 0.7448 74.48%
CYP3A4 substrate + 0.7249 72.49%
CYP2C9 substrate - 0.7965 79.65%
CYP2D6 substrate - 0.7950 79.50%
CYP3A4 inhibition + 0.5163 51.63%
CYP2C9 inhibition - 0.8283 82.83%
CYP2C19 inhibition - 0.7641 76.41%
CYP2D6 inhibition - 0.8729 87.29%
CYP1A2 inhibition - 0.8333 83.33%
CYP2C8 inhibition + 0.6795 67.95%
CYP inhibitory promiscuity - 0.9102 91.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.5869 58.69%
Eye corrosion - 0.9830 98.30%
Eye irritation - 0.9019 90.19%
Skin irritation - 0.7842 78.42%
Skin corrosion - 0.9161 91.61%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6268 62.68%
Micronuclear + 0.7100 71.00%
Hepatotoxicity + 0.5266 52.66%
skin sensitisation - 0.8541 85.41%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity + 0.5810 58.10%
Acute Oral Toxicity (c) III 0.5800 58.00%
Estrogen receptor binding + 0.7685 76.85%
Androgen receptor binding + 0.7459 74.59%
Thyroid receptor binding + 0.5250 52.50%
Glucocorticoid receptor binding + 0.6302 63.02%
Aromatase binding + 0.6496 64.96%
PPAR gamma + 0.6627 66.27%
Honey bee toxicity - 0.7366 73.66%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.7730 77.30%

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 99.41% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 97.77% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.67% 97.25%
CHEMBL202 P00374 Dihydrofolate reductase 95.99% 89.92%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 93.21% 95.50%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.99% 94.45%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 90.29% 100.00%
CHEMBL2581 P07339 Cathepsin D 89.85% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.82% 99.17%
CHEMBL4227 P25090 Lipoxin A4 receptor 87.45% 100.00%
CHEMBL5255 O00206 Toll-like receptor 4 87.36% 92.50%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 87.31% 96.21%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 86.51% 95.17%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 85.78% 93.10%
CHEMBL221 P23219 Cyclooxygenase-1 85.20% 90.17%
CHEMBL4581 P52732 Kinesin-like protein 1 84.48% 93.18%
CHEMBL3492 P49721 Proteasome Macropain subunit 84.27% 90.24%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.11% 95.89%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.74% 82.69%
CHEMBL233 P35372 Mu opioid receptor 83.33% 97.93%
CHEMBL2514 O95665 Neurotensin receptor 2 81.92% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.36% 93.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.89% 96.00%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 80.24% 98.33%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.13% 96.90%

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 163187817
LOTUS LTS0163085
wikiData Q104400979