1-But-3-enyl-2,3-dihydroinden-1-ol

Details

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Internal ID b24a81a5-c369-4e57-a805-76e8d0e67baf
Taxonomy Benzenoids > Indanes
IUPAC Name 1-but-3-enyl-2,3-dihydroinden-1-ol
SMILES (Canonical) C=CCCC1(CCC2=CC=CC=C21)O
SMILES (Isomeric) C=CCCC1(CCC2=CC=CC=C21)O
InChI InChI=1S/C13H16O/c1-2-3-9-13(14)10-8-11-6-4-5-7-12(11)13/h2,4-7,14H,1,3,8-10H2
InChI Key YPBIZYVRZQWVOM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H16O
Molecular Weight 188.26 g/mol
Exact Mass 188.120115130 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.79
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-But-3-enyl-2,3-dihydroinden-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9965 99.65%
Caco-2 + 0.8794 87.94%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.5038 50.38%
OATP2B1 inhibitior - 0.8605 86.05%
OATP1B1 inhibitior + 0.9371 93.71%
OATP1B3 inhibitior + 0.9440 94.40%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.7828 78.28%
P-glycoprotein inhibitior - 0.9794 97.94%
P-glycoprotein substrate - 0.9313 93.13%
CYP3A4 substrate - 0.5569 55.69%
CYP2C9 substrate - 0.5856 58.56%
CYP2D6 substrate + 0.4310 43.10%
CYP3A4 inhibition - 0.9122 91.22%
CYP2C9 inhibition - 0.7752 77.52%
CYP2C19 inhibition - 0.5276 52.76%
CYP2D6 inhibition - 0.8791 87.91%
CYP1A2 inhibition - 0.5918 59.18%
CYP2C8 inhibition - 0.8979 89.79%
CYP inhibitory promiscuity - 0.7434 74.34%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7300 73.00%
Carcinogenicity (trinary) Non-required 0.5696 56.96%
Eye corrosion - 0.9185 91.85%
Eye irritation + 0.9784 97.84%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9075 90.75%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6663 66.63%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.5071 50.71%
skin sensitisation + 0.6612 66.12%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.6795 67.95%
Acute Oral Toxicity (c) III 0.8448 84.48%
Estrogen receptor binding - 0.8195 81.95%
Androgen receptor binding - 0.5510 55.10%
Thyroid receptor binding - 0.7301 73.01%
Glucocorticoid receptor binding - 0.8607 86.07%
Aromatase binding - 0.6565 65.65%
PPAR gamma - 0.5892 58.92%
Honey bee toxicity - 0.9232 92.32%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9128 91.28%

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
CHEMBL240 Q12809 HERG 97.77% 89.76%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.96% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.92% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.84% 95.56%
CHEMBL3902 P09211 Glutathione S-transferase Pi 86.34% 93.81%
CHEMBL1841 P06241 Tyrosine-protein kinase FYN 83.34% 81.29%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 80.93% 94.62%
CHEMBL4208 P20618 Proteasome component C5 80.23% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.18% 86.33%

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.
Angelica gigas

Cross-Links

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PubChem 127005961
LOTUS LTS0262503
wikiData Q105351627