7-[2,3-dihydroxy-1-(1H-indol-3-yl)propyl]-1,2-bis(4-hydroxyphenyl)-3a-(2-methylpropyl)pyrrolo[1,2-a][3,1]benzoxazine-3,5-dione

Details

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Internal ID 5cc1aa3b-ee13-4fc8-9f21-065d125741c3
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 7-[2,3-dihydroxy-1-(1H-indol-3-yl)propyl]-1,2-bis(4-hydroxyphenyl)-3a-(2-methylpropyl)pyrrolo[1,2-a][3,1]benzoxazine-3,5-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C38H34N2O7/c1-21(2)18-38-36(45)34(22-7-12-25(42)13-8-22)35(23-9-14-26(43)15-10-23)40(38)31-16-11-24(17-28(31)37(46)47-38)33(32(44)20-41)29-19-39-30-6-4-3-5-27(29)30/h3-17,19,21,32-33,39,41-44H,18,20H2,1-2H3
InChI Key JGLJZSBEIRXXGB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C38H34N2O7
Molecular Weight 630.70 g/mol
Exact Mass 630.23660143 g/mol
Topological Polar Surface Area (TPSA) 143.00 Ų
XlogP 6.10
Atomic LogP (AlogP) 5.93
H-Bond Acceptor 8
H-Bond Donor 5
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-[2,3-dihydroxy-1-(1H-indol-3-yl)propyl]-1,2-bis(4-hydroxyphenyl)-3a-(2-methylpropyl)pyrrolo[1,2-a][3,1]benzoxazine-3,5-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9055 90.55%
Caco-2 - 0.8720 87.20%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7069 70.69%
OATP2B1 inhibitior + 0.5675 56.75%
OATP1B1 inhibitior + 0.8421 84.21%
OATP1B3 inhibitior + 0.9345 93.45%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9427 94.27%
BSEP inhibitior + 0.9968 99.68%
P-glycoprotein inhibitior + 0.8373 83.73%
P-glycoprotein substrate + 0.6787 67.87%
CYP3A4 substrate + 0.6888 68.88%
CYP2C9 substrate + 0.7989 79.89%
CYP2D6 substrate - 0.8462 84.62%
CYP3A4 inhibition - 0.8755 87.55%
CYP2C9 inhibition + 0.5297 52.97%
CYP2C19 inhibition - 0.6230 62.30%
CYP2D6 inhibition - 0.8750 87.50%
CYP1A2 inhibition - 0.6487 64.87%
CYP2C8 inhibition + 0.7107 71.07%
CYP inhibitory promiscuity - 0.6776 67.76%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.4948 49.48%
Eye corrosion - 0.9868 98.68%
Eye irritation - 0.9314 93.14%
Skin irritation - 0.7901 79.01%
Skin corrosion - 0.9325 93.25%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7480 74.80%
Micronuclear + 0.8700 87.00%
Hepatotoxicity - 0.6821 68.21%
skin sensitisation - 0.8526 85.26%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity - 0.8678 86.78%
Acute Oral Toxicity (c) III 0.6418 64.18%
Estrogen receptor binding + 0.8162 81.62%
Androgen receptor binding + 0.8504 85.04%
Thyroid receptor binding + 0.6297 62.97%
Glucocorticoid receptor binding + 0.7552 75.52%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.7541 75.41%
Honey bee toxicity - 0.7639 76.39%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6796 67.96%
Fish aquatic toxicity + 0.9352 93.52%

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
CHEMBL2581 P07339 Cathepsin D 99.69% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.95% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.81% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.06% 96.09%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 96.80% 83.10%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.97% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.31% 95.56%
CHEMBL242 Q92731 Estrogen receptor beta 95.19% 98.35%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 92.12% 93.10%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.09% 86.33%
CHEMBL2535 P11166 Glucose transporter 87.06% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.49% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.36% 99.23%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 85.17% 91.71%
CHEMBL3038469 P24941 CDK2/Cyclin A 84.90% 91.38%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 84.81% 89.44%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 84.08% 94.62%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.29% 99.15%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 83.12% 85.11%
CHEMBL3401 O75469 Pregnane X receptor 82.94% 94.73%
CHEMBL2996 Q05655 Protein kinase C delta 81.27% 97.79%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.52% 95.71%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 80.51% 89.67%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

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PubChem 162972729
LOTUS LTS0038132
wikiData Q104169500