(3aR,7aS)-3a-hydroxy-1-(3-phenylprop-2-enoyl)-2,3,7,7a-tetrahydroindol-6-one

Details

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Internal ID 404c452d-4d13-4739-a24c-fb9c5d4daeba
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives
IUPAC Name (3aR,7aS)-3a-hydroxy-1-(3-phenylprop-2-enoyl)-2,3,7,7a-tetrahydroindol-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H17NO3/c19-14-8-9-17(21)10-11-18(15(17)12-14)16(20)7-6-13-4-2-1-3-5-13/h1-9,15,21H,10-12H2/t15-,17-/m0/s1
InChI Key GIDUMOBEKYKEKW-RDJZCZTQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H17NO3
Molecular Weight 283.32 g/mol
Exact Mass 283.12084340 g/mol
Topological Polar Surface Area (TPSA) 57.60 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.56
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3aR,7aS)-3a-hydroxy-1-(3-phenylprop-2-enoyl)-2,3,7,7a-tetrahydroindol-6-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.5379 53.79%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7909 79.09%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9458 94.58%
OATP1B3 inhibitior + 0.9461 94.61%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6322 63.22%
BSEP inhibitior - 0.5617 56.17%
P-glycoprotein inhibitior - 0.8796 87.96%
P-glycoprotein substrate - 0.7877 78.77%
CYP3A4 substrate + 0.5198 51.98%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate - 0.8362 83.62%
CYP3A4 inhibition - 0.6824 68.24%
CYP2C9 inhibition - 0.8315 83.15%
CYP2C19 inhibition - 0.7624 76.24%
CYP2D6 inhibition - 0.8828 88.28%
CYP1A2 inhibition - 0.8526 85.26%
CYP2C8 inhibition - 0.8219 82.19%
CYP inhibitory promiscuity - 0.8174 81.74%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5567 55.67%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.9311 93.11%
Skin irritation - 0.7879 78.79%
Skin corrosion - 0.9219 92.19%
Ames mutagenesis - 0.7470 74.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4086 40.86%
Micronuclear + 0.6500 65.00%
Hepatotoxicity - 0.5656 56.56%
skin sensitisation - 0.8848 88.48%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.7796 77.96%
Acute Oral Toxicity (c) III 0.5842 58.42%
Estrogen receptor binding + 0.6650 66.50%
Androgen receptor binding + 0.7178 71.78%
Thyroid receptor binding - 0.6992 69.92%
Glucocorticoid receptor binding - 0.5541 55.41%
Aromatase binding + 0.5878 58.78%
PPAR gamma - 0.6812 68.12%
Honey bee toxicity - 0.9461 94.61%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.6663 66.63%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.91% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.00% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 94.03% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.71% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.63% 96.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.38% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.79% 89.00%
CHEMBL2581 P07339 Cathepsin D 87.46% 98.95%
CHEMBL5028 O14672 ADAM10 85.73% 97.50%
CHEMBL5805 Q9NR97 Toll-like receptor 8 83.70% 96.25%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.69% 93.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.26% 99.23%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 81.08% 94.62%
CHEMBL321 P14780 Matrix metalloproteinase 9 80.80% 92.12%

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.
Toussaintia orientalis

Cross-Links

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PubChem 163013965
LOTUS LTS0068867
wikiData Q105008903