(7S,8R)-7,8-dihydroxy-3,7-dimethyl-6-oxo-8H-isochromene-5-carbaldehyde

Details

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Internal ID 80cd1774-085b-44f1-bac9-0fbfcdc14cee
Taxonomy Organoheterocyclic compounds > Azaphilones
IUPAC Name (7S,8R)-7,8-dihydroxy-3,7-dimethyl-6-oxo-8H-isochromene-5-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H12O5/c1-6-3-7-8(4-13)10(14)12(2,16)11(15)9(7)5-17-6/h3-5,11,15-16H,1-2H3/t11-,12-/m1/s1
InChI Key QVMUHZHZYCDMAI-VXGBXAGGSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C12H12O5
Molecular Weight 236.22 g/mol
Exact Mass 236.06847348 g/mol
Topological Polar Surface Area (TPSA) 83.80 Ų
XlogP -1.20
Atomic LogP (AlogP) -0.01
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (7S,8R)-7,8-dihydroxy-3,7-dimethyl-6-oxo-8H-isochromene-5-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9579 95.79%
Caco-2 - 0.7688 76.88%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7356 73.56%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7866 78.66%
OATP1B3 inhibitior + 0.9838 98.38%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8680 86.80%
P-glycoprotein inhibitior - 0.9536 95.36%
P-glycoprotein substrate - 0.8790 87.90%
CYP3A4 substrate + 0.5550 55.50%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate - 0.8571 85.71%
CYP3A4 inhibition - 0.7549 75.49%
CYP2C9 inhibition - 0.7334 73.34%
CYP2C19 inhibition - 0.8520 85.20%
CYP2D6 inhibition - 0.8880 88.80%
CYP1A2 inhibition - 0.7744 77.44%
CYP2C8 inhibition - 0.8771 87.71%
CYP inhibitory promiscuity - 0.7671 76.71%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.4474 44.74%
Eye corrosion - 0.9787 97.87%
Eye irritation - 0.6562 65.62%
Skin irritation + 0.5177 51.77%
Skin corrosion - 0.8846 88.46%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8453 84.53%
Micronuclear + 0.6800 68.00%
Hepatotoxicity + 0.6740 67.40%
skin sensitisation - 0.7113 71.13%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.6200 62.00%
Acute Oral Toxicity (c) III 0.4514 45.14%
Estrogen receptor binding + 0.6262 62.62%
Androgen receptor binding - 0.6424 64.24%
Thyroid receptor binding - 0.5847 58.47%
Glucocorticoid receptor binding - 0.6508 65.08%
Aromatase binding - 0.7338 73.38%
PPAR gamma - 0.5282 52.82%
Honey bee toxicity - 0.8402 84.02%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.8574 85.74%

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
CHEMBL1951 P21397 Monoamine oxidase A 98.08% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.06% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.26% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.47% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 85.30% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.92% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.32% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.01% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.33% 96.09%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 92150829
LOTUS LTS0130130
wikiData Q105228758