3a,10b-Dimethyl-1,2,3,3a,5a,7,10b,10c-octahydro-5,8-dioxa-acephenanthrylene-4,9-dione

Details

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Internal ID 1f5753fb-e656-4710-a249-f1f955d22b75
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name 1,12-dimethyl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,7-diene-4,11-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H18O4/c1-15-4-3-5-16(2)13(15)11(20-14(16)18)6-9-8-19-12(17)7-10(9)15/h6-7,11,13H,3-5,8H2,1-2H3
InChI Key CADKOFRWMORBOD-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H18O4
Molecular Weight 274.31 g/mol
Exact Mass 274.12050905 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 1.80
Atomic LogP (AlogP) 2.15
H-Bond Acceptor 4
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 3a,10b-Dimethyl-1,2,3,3a,5a,7,10b,10c-octahydro-5,8-dioxa-acephenanthrylene-4,9-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 + 0.7588 75.88%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.8102 81.02%
OATP2B1 inhibitior - 0.8586 85.86%
OATP1B1 inhibitior + 0.9086 90.86%
OATP1B3 inhibitior + 0.9699 96.99%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.8709 87.09%
P-glycoprotein inhibitior - 0.8497 84.97%
P-glycoprotein substrate - 0.7564 75.64%
CYP3A4 substrate + 0.5709 57.09%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8917 89.17%
CYP3A4 inhibition - 0.7358 73.58%
CYP2C9 inhibition - 0.8638 86.38%
CYP2C19 inhibition - 0.9240 92.40%
CYP2D6 inhibition - 0.8673 86.73%
CYP1A2 inhibition - 0.5135 51.35%
CYP2C8 inhibition - 0.8719 87.19%
CYP inhibitory promiscuity - 0.7950 79.50%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5355 53.55%
Eye corrosion - 0.9854 98.54%
Eye irritation - 0.9659 96.59%
Skin irritation - 0.5378 53.78%
Skin corrosion - 0.8573 85.73%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8367 83.67%
Micronuclear - 0.6800 68.00%
Hepatotoxicity + 0.7927 79.27%
skin sensitisation - 0.7601 76.01%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.6384 63.84%
Acute Oral Toxicity (c) III 0.6205 62.05%
Estrogen receptor binding + 0.6781 67.81%
Androgen receptor binding + 0.5724 57.24%
Thyroid receptor binding - 0.6253 62.53%
Glucocorticoid receptor binding - 0.4682 46.82%
Aromatase binding - 0.5723 57.23%
PPAR gamma + 0.6755 67.55%
Honey bee toxicity - 0.7916 79.16%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9901 99.01%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.19% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.84% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.84% 100.00%
CHEMBL2581 P07339 Cathepsin D 88.48% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.21% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.16% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.09% 97.25%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.93% 82.69%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.97% 94.80%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.43% 99.23%

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 20649490
LOTUS LTS0051691
wikiData Q104950984