(2S)-5-hydroxy-2-methyl-2,3-dihydrochromen-4-one

Details

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Internal ID 8a947b82-81f2-442e-ac6e-fe132bb23439
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name (2S)-5-hydroxy-2-methyl-2,3-dihydrochromen-4-one
SMILES (Canonical) CC1CC(=O)C2=C(C=CC=C2O1)O
SMILES (Isomeric) C[C@H]1CC(=O)C2=C(C=CC=C2O1)O
InChI InChI=1S/C10H10O3/c1-6-5-8(12)10-7(11)3-2-4-9(10)13-6/h2-4,6,11H,5H2,1H3/t6-/m0/s1
InChI Key WHEIRCBYUYIIMR-LURJTMIESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H10O3
Molecular Weight 178.18 g/mol
Exact Mass 178.062994177 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.75
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S)-5-hydroxy-2-methyl-2,3-dihydrochromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9942 99.42%
Caco-2 + 0.7551 75.51%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6924 69.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9371 93.71%
OATP1B3 inhibitior + 0.9951 99.51%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9359 93.59%
P-glycoprotein inhibitior - 0.9795 97.95%
P-glycoprotein substrate - 0.9335 93.35%
CYP3A4 substrate - 0.5804 58.04%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.7840 78.40%
CYP3A4 inhibition - 0.8230 82.30%
CYP2C9 inhibition + 0.5089 50.89%
CYP2C19 inhibition + 0.7077 70.77%
CYP2D6 inhibition - 0.8387 83.87%
CYP1A2 inhibition + 0.9675 96.75%
CYP2C8 inhibition - 0.9561 95.61%
CYP inhibitory promiscuity - 0.7572 75.72%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9313 93.13%
Carcinogenicity (trinary) Non-required 0.4839 48.39%
Eye corrosion - 0.9394 93.94%
Eye irritation + 0.9636 96.36%
Skin irritation + 0.6000 60.00%
Skin corrosion - 0.9360 93.60%
Ames mutagenesis + 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8316 83.16%
Micronuclear + 0.6099 60.99%
Hepatotoxicity + 0.6658 66.58%
skin sensitisation - 0.7031 70.31%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.5193 51.93%
Acute Oral Toxicity (c) III 0.3559 35.59%
Estrogen receptor binding - 0.8631 86.31%
Androgen receptor binding + 0.5570 55.70%
Thyroid receptor binding - 0.7900 79.00%
Glucocorticoid receptor binding - 0.9104 91.04%
Aromatase binding - 0.9192 91.92%
PPAR gamma - 0.7022 70.22%
Honey bee toxicity - 0.9413 94.13%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.6913 69.13%

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 95.18% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.98% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.96% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.68% 99.23%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 86.57% 94.80%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.65% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.87% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 83.08% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 82.50% 94.73%

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.
Aquilaria sinensis
Garcinia dulcis
Pulicaria wightiana

Cross-Links

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PubChem 52914219
LOTUS LTS0027058
wikiData Q105305261