(3S,7R,8R)-7,8-dihydroxy-3-propyl-4,6,7,8-tetrahydro-3H-isochromene-1,5-dione

Details

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Internal ID 7a993137-d942-4f1c-9047-36687a32f533
Taxonomy Organoheterocyclic compounds > Benzopyrans
IUPAC Name (3S,7R,8R)-7,8-dihydroxy-3-propyl-4,6,7,8-tetrahydro-3H-isochromene-1,5-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H16O5/c1-2-3-6-4-7-8(13)5-9(14)11(15)10(7)12(16)17-6/h6,9,11,14-15H,2-5H2,1H3/t6-,9+,11-/m0/s1
InChI Key UJTPZWKMPAKALM-OIVXANJASA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O5
Molecular Weight 240.25 g/mol
Exact Mass 240.09977361 g/mol
Topological Polar Surface Area (TPSA) 83.80 Ų
XlogP -0.30
Atomic LogP (AlogP) 0.09
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S,7R,8R)-7,8-dihydroxy-3-propyl-4,6,7,8-tetrahydro-3H-isochromene-1,5-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8873 88.73%
Caco-2 - 0.5984 59.84%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.7274 72.74%
OATP2B1 inhibitior - 0.8514 85.14%
OATP1B1 inhibitior + 0.9116 91.16%
OATP1B3 inhibitior + 0.9489 94.89%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9409 94.09%
P-glycoprotein inhibitior - 0.9207 92.07%
P-glycoprotein substrate - 0.8652 86.52%
CYP3A4 substrate - 0.5807 58.07%
CYP2C9 substrate - 0.7974 79.74%
CYP2D6 substrate - 0.8846 88.46%
CYP3A4 inhibition - 0.5323 53.23%
CYP2C9 inhibition - 0.8776 87.76%
CYP2C19 inhibition - 0.8131 81.31%
CYP2D6 inhibition - 0.9018 90.18%
CYP1A2 inhibition - 0.8582 85.82%
CYP2C8 inhibition - 0.9601 96.01%
CYP inhibitory promiscuity - 0.9393 93.93%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5353 53.53%
Eye corrosion - 0.9862 98.62%
Eye irritation - 0.7725 77.25%
Skin irritation - 0.5639 56.39%
Skin corrosion - 0.9044 90.44%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6070 60.70%
Micronuclear - 0.7200 72.00%
Hepatotoxicity + 0.6839 68.39%
skin sensitisation - 0.8245 82.45%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity + 0.7002 70.02%
Acute Oral Toxicity (c) III 0.4617 46.17%
Estrogen receptor binding - 0.4860 48.60%
Androgen receptor binding - 0.5892 58.92%
Thyroid receptor binding - 0.5879 58.79%
Glucocorticoid receptor binding + 0.6440 64.40%
Aromatase binding - 0.8828 88.28%
PPAR gamma - 0.6416 64.16%
Honey bee toxicity - 0.9368 93.68%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9525 95.25%

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 96.18% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.58% 85.14%
CHEMBL221 P23219 Cyclooxygenase-1 90.41% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.96% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.65% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.54% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.34% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.36% 99.23%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.71% 96.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.25% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 80.18% 94.73%

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 101383035
LOTUS LTS0245356
wikiData Q105274206