4,8-Dimethyl-4a,5,6,7,8,8a-hexahydroisochromen-1-one

Details

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Internal ID 167f522e-cc43-4104-8e08-2e43eacd2d46
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives > Dihydropyranones
IUPAC Name 4,8-dimethyl-4a,5,6,7,8,8a-hexahydroisochromen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H16O2/c1-7-4-3-5-9-8(2)6-13-11(12)10(7)9/h6-7,9-10H,3-5H2,1-2H3
InChI Key IUFQXXXVUIYVOZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H16O2
Molecular Weight 180.24 g/mol
Exact Mass 180.115029749 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.50
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,8-Dimethyl-4a,5,6,7,8,8a-hexahydroisochromen-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 + 0.9969 99.69%
Caco-2 + 0.7881 78.81%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Plasma membrane 0.3758 37.58%
OATP2B1 inhibitior - 0.8412 84.12%
OATP1B1 inhibitior + 0.8969 89.69%
OATP1B3 inhibitior + 0.9556 95.56%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9393 93.93%
P-glycoprotein inhibitior - 0.9495 94.95%
P-glycoprotein substrate - 0.9344 93.44%
CYP3A4 substrate - 0.5342 53.42%
CYP2C9 substrate - 0.5853 58.53%
CYP2D6 substrate - 0.8323 83.23%
CYP3A4 inhibition - 0.8365 83.65%
CYP2C9 inhibition - 0.8623 86.23%
CYP2C19 inhibition - 0.6057 60.57%
CYP2D6 inhibition - 0.8926 89.26%
CYP1A2 inhibition + 0.5402 54.02%
CYP2C8 inhibition - 0.9761 97.61%
CYP inhibitory promiscuity - 0.8461 84.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5894 58.94%
Eye corrosion - 0.8954 89.54%
Eye irritation + 0.7843 78.43%
Skin irritation + 0.4926 49.26%
Skin corrosion - 0.9335 93.35%
Ames mutagenesis - 0.6737 67.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5618 56.18%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.7556 75.56%
skin sensitisation + 0.6545 65.45%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.5425 54.25%
Acute Oral Toxicity (c) III 0.7422 74.22%
Estrogen receptor binding - 0.8826 88.26%
Androgen receptor binding + 0.5277 52.77%
Thyroid receptor binding - 0.8193 81.93%
Glucocorticoid receptor binding - 0.8798 87.98%
Aromatase binding - 0.8742 87.42%
PPAR gamma - 0.8558 85.58%
Honey bee toxicity - 0.9465 94.65%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9724 97.24%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.26% 95.56%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 92.38% 86.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.86% 94.80%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.23% 97.09%
CHEMBL2581 P07339 Cathepsin D 86.96% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.68% 99.23%
CHEMBL5255 O00206 Toll-like receptor 4 80.07% 92.50%

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.
Nepeta nuda

Cross-Links

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PubChem 143226317
LOTUS LTS0166934
wikiData Q105120538