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

Details

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Internal ID 1b1bdef5-b496-49b7-97f0-417d62261dac
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 1,3,5,5-tetramethylcyclohexa-1,3-diene
SMILES (Canonical) CC1=CC(=CC(C1)(C)C)C
SMILES (Isomeric) CC1=CC(=CC(C1)(C)C)C
InChI InChI=1S/C10H16/c1-8-5-9(2)7-10(3,4)6-8/h5-6H,7H2,1-4H3
InChI Key SZHAWDAGEJWQJK-UHFFFAOYSA-N
Popularity 5 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 2.90
Atomic LogP (AlogP) 3.31
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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4724-89-4
1,3,5,5-tetramethylcyclohexa-1,3-diene
1,3-Cyclohexadiene, 1,3,5,5-tetramethyl-
LW73Z302UP
NSC 123453
NSC-123453
NSC123453
UNII-LW73Z302UP
1, 1,3,5,5-tetramethyl-
DTXSID0063575
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,3,5,5-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 + 0.9887 98.87%
Caco-2 + 0.9166 91.66%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Lysosomes 0.6309 63.09%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9467 94.67%
OATP1B3 inhibitior + 0.8951 89.51%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8875 88.75%
P-glycoprotein inhibitior - 0.9842 98.42%
P-glycoprotein substrate - 0.9405 94.05%
CYP3A4 substrate - 0.6036 60.36%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7968 79.68%
CYP3A4 inhibition - 0.7361 73.61%
CYP2C9 inhibition - 0.8108 81.08%
CYP2C19 inhibition - 0.8716 87.16%
CYP2D6 inhibition - 0.9227 92.27%
CYP1A2 inhibition - 0.8700 87.00%
CYP2C8 inhibition - 0.9748 97.48%
CYP inhibitory promiscuity - 0.6458 64.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5364 53.64%
Carcinogenicity (trinary) Warning 0.6356 63.56%
Eye corrosion + 0.6778 67.78%
Eye irritation + 0.9880 98.80%
Skin irritation + 0.7571 75.71%
Skin corrosion - 0.9353 93.53%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7155 71.55%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation + 0.9513 95.13%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.5715 57.15%
Nephrotoxicity + 0.7472 74.72%
Acute Oral Toxicity (c) III 0.8531 85.31%
Estrogen receptor binding - 0.9694 96.94%
Androgen receptor binding - 0.8548 85.48%
Thyroid receptor binding - 0.8708 87.08%
Glucocorticoid receptor binding - 0.9124 91.24%
Aromatase binding - 0.9132 91.32%
PPAR gamma - 0.9061 90.61%
Honey bee toxicity - 0.9497 94.97%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9763 97.63%

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 87.49% 91.11%
CHEMBL230 P35354 Cyclooxygenase-2 87.03% 89.63%
CHEMBL221 P23219 Cyclooxygenase-1 85.14% 90.17%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 84.40% 85.30%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.47% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.56% 95.56%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 81.24% 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.
Magnolia biondii
Magnolia denudata
Magnolia kobus
Magnolia salicifolia
Magnolia sprengeri

Cross-Links

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PubChem 78453
NPASS NPC80980