(3R)-8-hydroxy-5-(2-hydroxyethyl)-3-methyl-3,4-dihydroisochromen-1-one

Details

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Internal ID 73a79d87-750e-4147-b787-4c366cd7e29e
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name (3R)-8-hydroxy-5-(2-hydroxyethyl)-3-methyl-3,4-dihydroisochromen-1-one
SMILES (Canonical) CC1CC2=C(C=CC(=C2C(=O)O1)O)CCO
SMILES (Isomeric) C[C@@H]1CC2=C(C=CC(=C2C(=O)O1)O)CCO
InChI InChI=1S/C12H14O4/c1-7-6-9-8(4-5-13)2-3-10(14)11(9)12(15)16-7/h2-3,7,13-14H,4-6H2,1H3/t7-/m1/s1
InChI Key ZPQUKKQFTDITFH-SSDOTTSWSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H14O4
Molecular Weight 222.24 g/mol
Exact Mass 222.08920892 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.03
H-Bond Acceptor 4
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 (3R)-8-hydroxy-5-(2-hydroxyethyl)-3-methyl-3,4-dihydroisochromen-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9567 95.67%
Caco-2 + 0.6173 61.73%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7594 75.94%
OATP2B1 inhibitior - 0.8574 85.74%
OATP1B1 inhibitior + 0.8972 89.72%
OATP1B3 inhibitior + 0.9481 94.81%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.8292 82.92%
BSEP inhibitior - 0.8515 85.15%
P-glycoprotein inhibitior - 0.9152 91.52%
P-glycoprotein substrate - 0.8442 84.42%
CYP3A4 substrate - 0.5396 53.96%
CYP2C9 substrate + 0.6330 63.30%
CYP2D6 substrate - 0.8447 84.47%
CYP3A4 inhibition + 0.5000 50.00%
CYP2C9 inhibition - 0.8587 85.87%
CYP2C19 inhibition - 0.5629 56.29%
CYP2D6 inhibition - 0.7163 71.63%
CYP1A2 inhibition + 0.6259 62.59%
CYP2C8 inhibition - 0.8903 89.03%
CYP inhibitory promiscuity - 0.8158 81.58%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6898 68.98%
Eye corrosion - 0.9883 98.83%
Eye irritation + 0.8139 81.39%
Skin irritation - 0.7914 79.14%
Skin corrosion - 0.9690 96.90%
Ames mutagenesis + 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7510 75.10%
Micronuclear - 0.8500 85.00%
Hepatotoxicity + 0.6285 62.85%
skin sensitisation - 0.8769 87.69%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity + 0.6428 64.28%
Acute Oral Toxicity (c) III 0.5908 59.08%
Estrogen receptor binding - 0.5955 59.55%
Androgen receptor binding + 0.5943 59.43%
Thyroid receptor binding - 0.6444 64.44%
Glucocorticoid receptor binding - 0.5728 57.28%
Aromatase binding - 0.9333 93.33%
PPAR gamma - 0.5530 55.30%
Honey bee toxicity - 0.9020 90.20%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.8507 85.07%

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 98.73% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.93% 97.25%
CHEMBL2581 P07339 Cathepsin D 93.93% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 93.61% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.73% 95.56%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 86.60% 96.37%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.09% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 85.25% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.59% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.53% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.05% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.55% 99.23%

Plants that contains it

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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.
Euphorbia plumerioides

Cross-Links

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PubChem 14807795
LOTUS LTS0112952
wikiData Q105381128