(Z)-1-(2-indolyl)-2-phenylethylene

Details

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Internal ID 1dbb9e08-eb64-45bb-a609-d3feecba9a05
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles
IUPAC Name 2-[(Z)-2-phenylethenyl]-1H-indole
SMILES (Canonical) C1=CC=C(C=C1)C=CC2=CC3=CC=CC=C3N2
SMILES (Isomeric) C1=CC=C(C=C1)/C=C\C2=CC3=CC=CC=C3N2
InChI InChI=1S/C16H13N/c1-2-6-13(7-3-1)10-11-15-12-14-8-4-5-9-16(14)17-15/h1-12,17H/b11-10-
InChI Key IINBTRZAAVTTRD-KHPPLWFESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H13N
Molecular Weight 219.28 g/mol
Exact Mass 219.104799419 g/mol
Topological Polar Surface Area (TPSA) 15.80 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.34
H-Bond Acceptor 0
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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IINBTRZAAVTTRD-KHPPLWFESA-N
(Z)-1-(2-indolyl)-2-phenylethylene

2D Structure

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2D Structure of (Z)-1-(2-indolyl)-2-phenylethylene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.7545 75.45%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.5609 56.09%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9427 94.27%
OATP1B3 inhibitior + 0.9586 95.86%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.7713 77.13%
P-glycoprotein inhibitior - 0.9270 92.70%
P-glycoprotein substrate - 0.9745 97.45%
CYP3A4 substrate - 0.6983 69.83%
CYP2C9 substrate + 0.6236 62.36%
CYP2D6 substrate - 0.7048 70.48%
CYP3A4 inhibition - 0.7998 79.98%
CYP2C9 inhibition + 0.9339 93.39%
CYP2C19 inhibition + 0.9650 96.50%
CYP2D6 inhibition + 0.8067 80.67%
CYP1A2 inhibition + 0.9437 94.37%
CYP2C8 inhibition + 0.4666 46.66%
CYP inhibitory promiscuity + 0.8607 86.07%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.5086 50.86%
Eye corrosion - 0.8743 87.43%
Eye irritation + 0.9918 99.18%
Skin irritation + 0.7061 70.61%
Skin corrosion - 0.9227 92.27%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3783 37.83%
Micronuclear + 0.8359 83.59%
Hepatotoxicity + 0.5658 56.58%
skin sensitisation - 0.5814 58.14%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity - 0.6911 69.11%
Acute Oral Toxicity (c) III 0.6709 67.09%
Estrogen receptor binding + 0.9801 98.01%
Androgen receptor binding + 0.8220 82.20%
Thyroid receptor binding + 0.7559 75.59%
Glucocorticoid receptor binding - 0.4783 47.83%
Aromatase binding + 0.9584 95.84%
PPAR gamma + 0.8013 80.13%
Honey bee toxicity - 0.9214 92.14%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.7700 77.00%
Fish aquatic toxicity + 0.8896 88.96%

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
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 97.39% 94.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.94% 91.11%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 92.87% 91.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.47% 96.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.85% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.24% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.06% 86.33%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 86.68% 94.23%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 86.10% 94.08%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 85.75% 85.49%
CHEMBL2708 Q16584 Mitogen-activated protein kinase kinase kinase 11 85.67% 81.14%
CHEMBL1937 Q92769 Histone deacetylase 2 85.45% 94.75%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 82.86% 89.44%
CHEMBL230 P35354 Cyclooxygenase-2 82.00% 89.63%
CHEMBL3401 O75469 Pregnane X receptor 80.98% 94.73%
CHEMBL2535 P11166 Glucose transporter 80.25% 98.75%
CHEMBL4302 P08183 P-glycoprotein 1 80.04% 92.98%

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.
Digitalis lanata

Cross-Links

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PubChem 67937868
NPASS NPC164268