2-Methyl-5,7-dimethylene-1,8-nonadiene

Details

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Internal ID 621c1e93-cc45-4f84-af13-7a217a0d5dcb
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Acyclic olefins > Alkatetraenes
IUPAC Name 2-methyl-5,7-dimethylidenenona-1,8-diene
SMILES (Canonical) CC(=C)CCC(=C)CC(=C)C=C
SMILES (Isomeric) CC(=C)CCC(=C)CC(=C)C=C
InChI InChI=1S/C12H18/c1-6-11(4)9-12(5)8-7-10(2)3/h6H,1-2,4-5,7-9H2,3H3
InChI Key RCZAYHKXHPHBPX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H18
Molecular Weight 162.27 g/mol
Exact Mass 162.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.40
Atomic LogP (AlogP) 4.03
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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2-Methyl-5,7-dimethylene-1,8-nonadiene
RCZAYHKXHPHBPX-UHFFFAOYSA-N
2-Methyl-5,7-dimethylene-1,8-nonadiene #

2D Structure

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2D Structure of 2-Methyl-5,7-dimethylene-1,8-nonadiene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9834 98.34%
Caco-2 + 0.8359 83.59%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.3915 39.15%
OATP2B1 inhibitior - 0.8567 85.67%
OATP1B1 inhibitior + 0.9043 90.43%
OATP1B3 inhibitior + 0.9452 94.52%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9115 91.15%
P-glycoprotein inhibitior - 0.9650 96.50%
P-glycoprotein substrate - 0.9119 91.19%
CYP3A4 substrate - 0.6477 64.77%
CYP2C9 substrate - 0.8209 82.09%
CYP2D6 substrate - 0.7550 75.50%
CYP3A4 inhibition - 0.9596 95.96%
CYP2C9 inhibition - 0.9281 92.81%
CYP2C19 inhibition - 0.8941 89.41%
CYP2D6 inhibition - 0.9340 93.40%
CYP1A2 inhibition - 0.6369 63.69%
CYP2C8 inhibition - 0.9466 94.66%
CYP inhibitory promiscuity - 0.6249 62.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5400 54.00%
Carcinogenicity (trinary) Warning 0.4978 49.78%
Eye corrosion + 0.9215 92.15%
Eye irritation + 0.9353 93.53%
Skin irritation + 0.8233 82.33%
Skin corrosion - 0.9140 91.40%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5282 52.82%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation + 0.9193 91.93%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.8020 80.20%
Acute Oral Toxicity (c) III 0.7552 75.52%
Estrogen receptor binding - 0.9350 93.50%
Androgen receptor binding - 0.8822 88.22%
Thyroid receptor binding - 0.7207 72.07%
Glucocorticoid receptor binding - 0.8679 86.79%
Aromatase binding - 0.7958 79.58%
PPAR gamma - 0.8355 83.55%
Honey bee toxicity - 0.8406 84.06%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity + 0.9856 98.56%

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
CHEMBL4040 P28482 MAP kinase ERK2 89.08% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.80% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.88% 91.11%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 85.78% 97.34%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.80% 89.34%
CHEMBL2581 P07339 Cathepsin D 80.36% 98.95%

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.
Mentha arvensis
Mentha canadensis

Cross-Links

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PubChem 561666
NPASS NPC110253