3,7-dimethyl-3,4-dihydro-1H-isochromen-8-ol

Details

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Internal ID 52994173-39f3-4d6e-8270-d28f97739c65
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name 3,7-dimethyl-3,4-dihydro-1H-isochromen-8-ol
SMILES (Canonical) CC1CC2=C(CO1)C(=C(C=C2)C)O
SMILES (Isomeric) CC1CC2=C(CO1)C(=C(C=C2)C)O
InChI InChI=1S/C11H14O2/c1-7-3-4-9-5-8(2)13-6-10(9)11(7)12/h3-4,8,12H,5-6H2,1-2H3
InChI Key DUCHRZYTOZUUJA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H14O2
Molecular Weight 178.23 g/mol
Exact Mass 178.099379685 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.16
H-Bond Acceptor 2
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 3,7-dimethyl-3,4-dihydro-1H-isochromen-8-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9938 99.38%
Caco-2 + 0.7198 71.98%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.6736 67.36%
OATP2B1 inhibitior - 0.8544 85.44%
OATP1B1 inhibitior + 0.9160 91.60%
OATP1B3 inhibitior + 0.9549 95.49%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9062 90.62%
P-glycoprotein inhibitior - 0.9827 98.27%
P-glycoprotein substrate - 0.8468 84.68%
CYP3A4 substrate - 0.5344 53.44%
CYP2C9 substrate - 0.8074 80.74%
CYP2D6 substrate + 0.4113 41.13%
CYP3A4 inhibition - 0.7515 75.15%
CYP2C9 inhibition - 0.7341 73.41%
CYP2C19 inhibition + 0.6057 60.57%
CYP2D6 inhibition - 0.9083 90.83%
CYP1A2 inhibition + 0.9119 91.19%
CYP2C8 inhibition - 0.8515 85.15%
CYP inhibitory promiscuity - 0.7909 79.09%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9113 91.13%
Carcinogenicity (trinary) Non-required 0.5778 57.78%
Eye corrosion - 0.9746 97.46%
Eye irritation + 0.6349 63.49%
Skin irritation - 0.7124 71.24%
Skin corrosion - 0.9278 92.78%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5719 57.19%
Micronuclear - 0.7782 77.82%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation - 0.7123 71.23%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.8454 84.54%
Acute Oral Toxicity (c) III 0.6256 62.56%
Estrogen receptor binding - 0.8532 85.32%
Androgen receptor binding - 0.5445 54.45%
Thyroid receptor binding - 0.7421 74.21%
Glucocorticoid receptor binding - 0.8801 88.01%
Aromatase binding - 0.9282 92.82%
PPAR gamma - 0.7392 73.92%
Honey bee toxicity - 0.9709 97.09%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9328 93.28%

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 96.45% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 95.23% 91.49%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 84.03% 93.40%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.71% 95.56%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.26% 92.94%
CHEMBL3401 O75469 Pregnane X receptor 82.89% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.43% 96.09%
CHEMBL2581 P07339 Cathepsin D 82.23% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.29% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.48% 86.33%

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 150095358
LOTUS LTS0229250
wikiData Q103818711