1,5,5,6-Tetramethyl-1,3-cyclohexadiene

Details

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Internal ID c7e08810-ee2c-4b47-a812-0db037298a85
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 1,5,5,6-tetramethylcyclohexa-1,3-diene
SMILES (Canonical) CC1C(=CC=CC1(C)C)C
SMILES (Isomeric) CC1C(=CC=CC1(C)C)C
InChI InChI=1S/C10H16/c1-8-6-5-7-10(3,4)9(8)2/h5-7,9H,1-4H3
InChI Key LKNRSUKTEIJIAS-UHFFFAOYSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16
Molecular Weight 136.23 g/mol
Exact Mass 136.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.16
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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alpha-Pyronene
1,5,5,6-tetramethylcyclohexa-1,3-diene
514-94-3
1,5,5,6-TETRAMETHYL-1,3-CYCLOHEXADIENE
1,3-Cyclohexadiene, 1,5,5,6-tetramethyl-
DTXSID90965715
LKNRSUKTEIJIAS-UHFFFAOYSA-N
AKOS006275463
1,5,5,6-Tetramethyl-1,3-cyclohexadiene #

2D Structure

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2D Structure of 1,5,5,6-Tetramethyl-1,3-cyclohexadiene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9904 99.04%
Caco-2 + 0.8484 84.84%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.5869 58.69%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9448 94.48%
OATP1B3 inhibitior + 0.9031 90.31%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8697 86.97%
P-glycoprotein inhibitior - 0.9737 97.37%
P-glycoprotein substrate - 0.9315 93.15%
CYP3A4 substrate - 0.5995 59.95%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.8277 82.77%
CYP3A4 inhibition - 0.7269 72.69%
CYP2C9 inhibition - 0.8135 81.35%
CYP2C19 inhibition - 0.8145 81.45%
CYP2D6 inhibition - 0.9398 93.98%
CYP1A2 inhibition - 0.8488 84.88%
CYP2C8 inhibition - 0.9413 94.13%
CYP inhibitory promiscuity + 0.5551 55.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5283 52.83%
Carcinogenicity (trinary) Warning 0.5489 54.89%
Eye corrosion + 0.7582 75.82%
Eye irritation + 0.9251 92.51%
Skin irritation + 0.7344 73.44%
Skin corrosion - 0.8942 89.42%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5711 57.11%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation + 0.9462 94.62%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.6799 67.99%
Nephrotoxicity - 0.5592 55.92%
Acute Oral Toxicity (c) III 0.8110 81.10%
Estrogen receptor binding - 0.9344 93.44%
Androgen receptor binding - 0.8310 83.10%
Thyroid receptor binding - 0.8533 85.33%
Glucocorticoid receptor binding - 0.8888 88.88%
Aromatase binding - 0.9004 90.04%
PPAR gamma - 0.8702 87.02%
Honey bee toxicity - 0.9015 90.15%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.7700 77.00%
Fish aquatic toxicity + 0.9716 97.16%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.81% 96.09%
CHEMBL3492 P49721 Proteasome Macropain subunit 82.61% 90.24%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 82.28% 86.00%

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.
Anethum graveolens
Angelica acutiloba
Angelica gigas
Angelica sinensis
Leonurus japonicus

Cross-Links

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PubChem 10581
NPASS NPC238960
LOTUS LTS0072806
wikiData Q82948018