(1Z)-1-butylidene-8-hydroxyisochromen-4-one

Details

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Internal ID 0b678416-b8b7-484a-9462-bbff2bc2651e
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name (1Z)-1-butylidene-8-hydroxyisochromen-4-one
SMILES (Canonical) CCCC=C1C2=C(C=CC=C2O)C(=O)CO1
SMILES (Isomeric) CCC/C=C\1/C2=C(C=CC=C2O)C(=O)CO1
InChI InChI=1S/C13H14O3/c1-2-3-7-12-13-9(11(15)8-16-12)5-4-6-10(13)14/h4-7,14H,2-3,8H2,1H3/b12-7-
InChI Key MPUFGOPEVKRAGE-GHXNOFRVSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H14O3
Molecular Weight 218.25 g/mol
Exact Mass 218.094294304 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.75
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 (1Z)-1-butylidene-8-hydroxyisochromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 + 0.9047 90.47%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.5542 55.42%
OATP2B1 inhibitior - 0.8598 85.98%
OATP1B1 inhibitior + 0.9134 91.34%
OATP1B3 inhibitior + 0.9700 97.00%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7960 79.60%
P-glycoprotein inhibitior - 0.9545 95.45%
P-glycoprotein substrate - 0.8270 82.70%
CYP3A4 substrate - 0.5334 53.34%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7417 74.17%
CYP3A4 inhibition - 0.8131 81.31%
CYP2C9 inhibition - 0.6830 68.30%
CYP2C19 inhibition + 0.7806 78.06%
CYP2D6 inhibition - 0.8603 86.03%
CYP1A2 inhibition + 0.8970 89.70%
CYP2C8 inhibition - 0.8412 84.12%
CYP inhibitory promiscuity + 0.6301 63.01%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9218 92.18%
Carcinogenicity (trinary) Non-required 0.5994 59.94%
Eye corrosion - 0.9700 97.00%
Eye irritation + 0.8795 87.95%
Skin irritation - 0.7574 75.74%
Skin corrosion - 0.9663 96.63%
Ames mutagenesis + 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5945 59.45%
Micronuclear - 0.8300 83.00%
Hepatotoxicity + 0.6442 64.42%
skin sensitisation - 0.5866 58.66%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.6434 64.34%
Acute Oral Toxicity (c) III 0.5399 53.99%
Estrogen receptor binding + 0.7101 71.01%
Androgen receptor binding - 0.5223 52.23%
Thyroid receptor binding + 0.5331 53.31%
Glucocorticoid receptor binding - 0.5351 53.51%
Aromatase binding - 0.7838 78.38%
PPAR gamma + 0.7771 77.71%
Honey bee toxicity - 0.9614 96.14%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.8943 89.43%

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 97.88% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.88% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.26% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.11% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 89.03% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.05% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.64% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.44% 99.23%
CHEMBL1951 P21397 Monoamine oxidase A 83.17% 91.49%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.89% 100.00%

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.
Conioselinum anthriscoides
Fritillaria delavayi
Fritillaria przewalskii

Cross-Links

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PubChem 5315862
NPASS NPC105784