3-Prop-1-ynylisochromen-1-one

Details

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Internal ID dcb3946e-e0ba-48f9-8be3-a06ab64621a7
Taxonomy Phenylpropanoids and polyketides > Isocoumarins and derivatives
IUPAC Name 3-prop-1-ynylisochromen-1-one
SMILES (Canonical) CC#CC1=CC2=CC=CC=C2C(=O)O1
SMILES (Isomeric) CC#CC1=CC2=CC=CC=C2C(=O)O1
InChI InChI=1S/C12H8O2/c1-2-5-10-8-9-6-3-4-7-11(9)12(13)14-10/h3-4,6-8H,1H3
InChI Key OSTJORVQJLDDPC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H8O2
Molecular Weight 184.19 g/mol
Exact Mass 184.052429494 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.16
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Prop-1-ynylisochromen-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9958 99.58%
Caco-2 + 0.7856 78.56%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.5399 53.99%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9371 93.71%
OATP1B3 inhibitior + 0.9847 98.47%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8177 81.77%
P-glycoprotein inhibitior - 0.9493 94.93%
P-glycoprotein substrate - 0.9510 95.10%
CYP3A4 substrate - 0.5834 58.34%
CYP2C9 substrate - 0.6778 67.78%
CYP2D6 substrate - 0.8568 85.68%
CYP3A4 inhibition - 0.6965 69.65%
CYP2C9 inhibition - 0.7380 73.80%
CYP2C19 inhibition - 0.7149 71.49%
CYP2D6 inhibition - 0.9572 95.72%
CYP1A2 inhibition + 0.9452 94.52%
CYP2C8 inhibition - 0.8705 87.05%
CYP inhibitory promiscuity - 0.7390 73.90%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8713 87.13%
Carcinogenicity (trinary) Warning 0.4415 44.15%
Eye corrosion - 0.8784 87.84%
Eye irritation + 0.8571 85.71%
Skin irritation + 0.6941 69.41%
Skin corrosion - 0.9624 96.24%
Ames mutagenesis + 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7872 78.72%
Micronuclear + 0.6459 64.59%
Hepatotoxicity + 0.8574 85.74%
skin sensitisation - 0.7193 71.93%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.5171 51.71%
Acute Oral Toxicity (c) III 0.7541 75.41%
Estrogen receptor binding - 0.5436 54.36%
Androgen receptor binding + 0.7058 70.58%
Thyroid receptor binding - 0.6044 60.44%
Glucocorticoid receptor binding + 0.5448 54.48%
Aromatase binding + 0.5779 57.79%
PPAR gamma - 0.7468 74.68%
Honey bee toxicity - 0.9202 92.02%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.8559 85.59%

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 96.67% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.09% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 88.73% 94.73%
CHEMBL2581 P07339 Cathepsin D 88.40% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.51% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.50% 99.23%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.18% 93.65%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.63% 94.00%
CHEMBL2039 P27338 Monoamine oxidase B 84.15% 92.51%
CHEMBL2535 P11166 Glucose transporter 83.13% 98.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.55% 89.00%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 80.68% 96.42%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.18% 96.67%

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.
Artemisia xanthochroa

Cross-Links

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PubChem 14730875
LOTUS LTS0223021
wikiData Q105199318