8H-Furo(3,2-h)(1)benzopyran-8-one

Details

Top
Internal ID c7770dfd-e19f-40d2-8d89-18170c51e087
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Furanocoumarins > Angular furanocoumarins
IUPAC Name furo[3,2-h]chromen-8-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H6O3/c12-9-4-3-7-1-2-8-5-6-13-10(8)11(7)14-9/h1-6H
InChI Key MLMVLVJMKDPYBM-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

Top
Molecular Formula C11H6O3
Molecular Weight 186.16 g/mol
Exact Mass 186.031694049 g/mol
Topological Polar Surface Area (TPSA) 39.40 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.54
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

Top
5768-44-5
8H-Furo(3,2-h)(1)benzopyran-8-one
isosporalen
DTXSID00206383

2D Structure

Top
2D Structure of 8H-Furo(3,2-h)(1)benzopyran-8-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9949 99.49%
Caco-2 + 0.7885 78.85%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6792 67.92%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9568 95.68%
OATP1B3 inhibitior + 0.9414 94.14%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8334 83.34%
P-glycoprotein inhibitior - 0.9009 90.09%
P-glycoprotein substrate - 0.9844 98.44%
CYP3A4 substrate - 0.7811 78.11%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8441 84.41%
CYP3A4 inhibition + 0.5510 55.10%
CYP2C9 inhibition - 0.6470 64.70%
CYP2C19 inhibition + 0.6212 62.12%
CYP2D6 inhibition + 0.5914 59.14%
CYP1A2 inhibition + 0.8787 87.87%
CYP2C8 inhibition - 0.9354 93.54%
CYP inhibitory promiscuity - 0.6108 61.08%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Warning 0.5203 52.03%
Eye corrosion - 0.9114 91.14%
Eye irritation + 0.9617 96.17%
Skin irritation + 0.8200 82.00%
Skin corrosion - 0.9718 97.18%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6888 68.88%
Micronuclear + 0.7500 75.00%
Hepatotoxicity + 0.8375 83.75%
skin sensitisation - 0.5818 58.18%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.5749 57.49%
Acute Oral Toxicity (c) II 0.7326 73.26%
Estrogen receptor binding + 0.6097 60.97%
Androgen receptor binding + 0.7631 76.31%
Thyroid receptor binding - 0.5235 52.35%
Glucocorticoid receptor binding + 0.7423 74.23%
Aromatase binding + 0.8530 85.30%
PPAR gamma + 0.6710 67.10%
Honey bee toxicity - 0.9003 90.03%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.8522 85.22%

Targets

Top

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
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.58% 99.23%
CHEMBL2581 P07339 Cathepsin D 86.13% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.95% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.90% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.17% 91.11%

Plants that contains it

Top
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 keiskei
Bituminaria morisiana

Cross-Links

Top
PubChem 3083917
LOTUS LTS0067564
wikiData Q83080220