cis-4-Hydroxymellein

Details

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Internal ID 308be42d-9d64-43fe-9aea-5c2ada102804
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name (3R,4R)-4,8-dihydroxy-3-methyl-3,4-dihydroisochromen-1-one
SMILES (Canonical) CC1C(C2=C(C(=CC=C2)O)C(=O)O1)O
SMILES (Isomeric) C[C@@H]1[C@@H](C2=C(C(=CC=C2)O)C(=O)O1)O
InChI InChI=1S/C10H10O4/c1-5-9(12)6-3-2-4-7(11)8(6)10(13)14-5/h2-5,9,11-12H,1H3/t5-,9+/m1/s1
InChI Key STSOHAOGZMLWFR-ANLVUFKYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C10H10O4
Molecular Weight 194.18 g/mol
Exact Mass 194.05790880 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 1.30
Atomic LogP (AlogP) 0.98
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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4-Hydroxymellein, cis-
cis-4-Hydroxymellein, (-)-
(3R,4R)-cis-4-Hydroxymellein
cis-(3R,4R)-4-Hydroxymellein
YJ8535DF71
UNII-YJ8535DF71
Isocoumarin, 3,4-dihydro-4,8-dihydroxy-3-methyl-, cis-
1H-2-Benzopyran-1-one, 3,4-dihydro-4,8-dihydroxy-3-methyl-, (3R,4R)-
1H-2-Benzopyran-1-one, 3,4-dihydro-4,8-dihydroxy-3-methyl-, (3R-cis)-
32885-83-9
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of cis-4-Hydroxymellein

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9643 96.43%
Caco-2 - 0.7334 73.34%
Blood Brain Barrier - 0.8750 87.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7400 74.00%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8822 88.22%
OATP1B3 inhibitior + 0.9663 96.63%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9785 97.85%
P-glycoprotein inhibitior - 0.9727 97.27%
P-glycoprotein substrate - 0.9404 94.04%
CYP3A4 substrate - 0.5437 54.37%
CYP2C9 substrate - 0.5773 57.73%
CYP2D6 substrate - 0.8491 84.91%
CYP3A4 inhibition - 0.8976 89.76%
CYP2C9 inhibition - 0.6639 66.39%
CYP2C19 inhibition - 0.8916 89.16%
CYP2D6 inhibition - 0.9570 95.70%
CYP1A2 inhibition + 0.8008 80.08%
CYP2C8 inhibition - 0.9144 91.44%
CYP inhibitory promiscuity - 0.7294 72.94%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6235 62.35%
Eye corrosion - 0.9542 95.42%
Eye irritation + 0.6891 68.91%
Skin irritation + 0.6880 68.80%
Skin corrosion - 0.9335 93.35%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8767 87.67%
Micronuclear + 0.9300 93.00%
Hepatotoxicity + 0.7806 78.06%
skin sensitisation - 0.7791 77.91%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.5693 56.93%
Acute Oral Toxicity (c) III 0.6350 63.50%
Estrogen receptor binding - 0.8099 80.99%
Androgen receptor binding - 0.5681 56.81%
Thyroid receptor binding - 0.6652 66.52%
Glucocorticoid receptor binding - 0.8140 81.40%
Aromatase binding - 0.8900 89.00%
PPAR gamma - 0.6797 67.97%
Honey bee toxicity - 0.9426 94.26%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.8753 87.53%

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 96.25% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.82% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.96% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 91.99% 91.49%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.14% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 88.05% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.94% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.50% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.28% 85.14%

Cross-Links

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PubChem 10420140
NPASS NPC303187
LOTUS LTS0036641
wikiData Q27294545