(3R)-8-hydroxy-3,7-dimethyl-3,4-dihydroisochromen-1-one

Details

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Internal ID 80a40f3a-5c69-4bd3-beb0-ff46b30780ae
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name (3R)-8-hydroxy-3,7-dimethyl-3,4-dihydroisochromen-1-one
SMILES (Canonical) CC1CC2=C(C(=C(C=C2)C)O)C(=O)O1
SMILES (Isomeric) C[C@@H]1CC2=C(C(=C(C=C2)C)O)C(=O)O1
InChI InChI=1S/C11H12O3/c1-6-3-4-8-5-7(2)14-11(13)9(8)10(6)12/h3-4,7,12H,5H2,1-2H3/t7-/m1/s1
InChI Key SLYRNFYMGDTQEZ-SSDOTTSWSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H12O3
Molecular Weight 192.21 g/mol
Exact Mass 192.078644241 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.80
Atomic LogP (AlogP) 1.80
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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SCHEMBL16870458

2D Structure

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2D Structure of (3R)-8-hydroxy-3,7-dimethyl-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 + 0.9855 98.55%
Caco-2 + 0.6972 69.72%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7124 71.24%
OATP2B1 inhibitior - 0.8617 86.17%
OATP1B1 inhibitior + 0.8878 88.78%
OATP1B3 inhibitior + 0.9871 98.71%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9004 90.04%
P-glycoprotein inhibitior - 0.9647 96.47%
P-glycoprotein substrate - 0.9384 93.84%
CYP3A4 substrate - 0.5425 54.25%
CYP2C9 substrate + 0.6383 63.83%
CYP2D6 substrate - 0.8466 84.66%
CYP3A4 inhibition - 0.8872 88.72%
CYP2C9 inhibition - 0.5492 54.92%
CYP2C19 inhibition - 0.7965 79.65%
CYP2D6 inhibition - 0.9048 90.48%
CYP1A2 inhibition + 0.7144 71.44%
CYP2C8 inhibition - 0.9395 93.95%
CYP inhibitory promiscuity - 0.8687 86.87%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Non-required 0.5616 56.16%
Eye corrosion - 0.9712 97.12%
Eye irritation + 0.8245 82.45%
Skin irritation + 0.5194 51.94%
Skin corrosion - 0.9384 93.84%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6841 68.41%
Micronuclear + 0.6318 63.18%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation - 0.7203 72.03%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.6954 69.54%
Acute Oral Toxicity (c) I 0.5465 54.65%
Estrogen receptor binding - 0.7736 77.36%
Androgen receptor binding + 0.6369 63.69%
Thyroid receptor binding - 0.7201 72.01%
Glucocorticoid receptor binding - 0.8442 84.42%
Aromatase binding - 0.8493 84.93%
PPAR gamma - 0.6214 62.14%
Honey bee toxicity - 0.9719 97.19%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9041 90.41%

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 96.30% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 95.07% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.47% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.61% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 89.40% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.80% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.58% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.66% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.09% 94.00%

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.
Endlicheria sericea
Salsola micranthera
Symplocos glomerata

Cross-Links

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PubChem 118203913
LOTUS LTS0062957
wikiData Q105262563