(3R)-7-hydroxy-5-methylmellein

Details

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Internal ID 7adb7347-2d61-48f9-8e30-aec9714184c4
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name (3R)-7,8-dihydroxy-3,5-dimethyl-3,4-dihydroisochromen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H12O4/c1-5-3-8(12)10(13)9-7(5)4-6(2)15-11(9)14/h3,6,12-13H,4H2,1-2H3/t6-/m1/s1
InChI Key XITCGWRCIXZQJW-ZCFIWIBFSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C11H12O4
Molecular Weight 208.21 g/mol
Exact Mass 208.07355886 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 2.40
Atomic LogP (AlogP) 1.51
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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(3R)-3,5-Dimethyl-7,8-dihydroxy-3,4-dihydro-1H-2-benzopyran-1-one
(3R)-7,8-dihydroxy-3,5-dimethyl-3,4-dihydroisochromen-1-one

2D Structure

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2D Structure of (3R)-7-hydroxy-5-methylmellein

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9007 90.07%
Caco-2 - 0.5779 57.79%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6355 63.55%
OATP2B1 inhibitior - 0.8576 85.76%
OATP1B1 inhibitior + 0.9112 91.12%
OATP1B3 inhibitior + 0.9786 97.86%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9406 94.06%
P-glycoprotein inhibitior - 0.9467 94.67%
P-glycoprotein substrate - 0.9414 94.14%
CYP3A4 substrate - 0.5383 53.83%
CYP2C9 substrate - 0.5555 55.55%
CYP2D6 substrate - 0.8498 84.98%
CYP3A4 inhibition - 0.9042 90.42%
CYP2C9 inhibition - 0.8254 82.54%
CYP2C19 inhibition - 0.8829 88.29%
CYP2D6 inhibition - 0.8136 81.36%
CYP1A2 inhibition + 0.8247 82.47%
CYP2C8 inhibition - 0.8679 86.79%
CYP inhibitory promiscuity - 0.9124 91.24%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6385 63.85%
Eye corrosion - 0.9852 98.52%
Eye irritation - 0.4791 47.91%
Skin irritation - 0.5709 57.09%
Skin corrosion - 0.8971 89.71%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6645 66.45%
Micronuclear + 0.5259 52.59%
Hepatotoxicity + 0.7816 78.16%
skin sensitisation - 0.7882 78.82%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.7244 72.44%
Acute Oral Toxicity (c) III 0.3984 39.84%
Estrogen receptor binding - 0.7345 73.45%
Androgen receptor binding + 0.5853 58.53%
Thyroid receptor binding - 0.6338 63.38%
Glucocorticoid receptor binding - 0.6660 66.60%
Aromatase binding - 0.8911 89.11%
PPAR gamma - 0.5526 55.26%
Honey bee toxicity - 0.9579 95.79%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9574 95.74%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.21% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.23% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.31% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 90.80% 93.40%
CHEMBL2581 P07339 Cathepsin D 89.76% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.61% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.02% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 87.93% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.62% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.07% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.93% 99.15%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.27% 85.14%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.17% 93.65%

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 24799337
LOTUS LTS0221903
wikiData Q105328738