1,1-Dimethyl-3-methylidene-2-(3-methyl-7-methylidenenona-3,8-dienyl)cyclohexane

Details

Top
Internal ID 91f78e6c-9f25-42ab-a373-073af758f752
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1,1-dimethyl-3-methylidene-2-(3-methyl-7-methylidenenona-3,8-dienyl)cyclohexane
SMILES (Canonical) CC(=CCCC(=C)C=C)CCC1C(=C)CCCC1(C)C
SMILES (Isomeric) CC(=CCCC(=C)C=C)CCC1C(=C)CCCC1(C)C
InChI InChI=1S/C20H32/c1-7-16(2)10-8-11-17(3)13-14-19-18(4)12-9-15-20(19,5)6/h7,11,19H,1-2,4,8-10,12-15H2,3,5-6H3
InChI Key JYLFEIJIZTXUNT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C20H32
Molecular Weight 272.50 g/mol
Exact Mass 272.250401021 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 7.60
Atomic LogP (AlogP) 6.62
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 1,1-Dimethyl-3-methylidene-2-(3-methyl-7-methylidenenona-3,8-dienyl)cyclohexane

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9879 98.79%
Caco-2 + 0.6896 68.96%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.5851 58.51%
OATP2B1 inhibitior - 0.8541 85.41%
OATP1B1 inhibitior + 0.8329 83.29%
OATP1B3 inhibitior - 0.3180 31.80%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.5104 51.04%
P-glycoprotein inhibitior - 0.8004 80.04%
P-glycoprotein substrate - 0.7823 78.23%
CYP3A4 substrate + 0.5615 56.15%
CYP2C9 substrate - 0.8128 81.28%
CYP2D6 substrate - 0.7875 78.75%
CYP3A4 inhibition - 0.8603 86.03%
CYP2C9 inhibition - 0.8620 86.20%
CYP2C19 inhibition - 0.8554 85.54%
CYP2D6 inhibition - 0.9480 94.80%
CYP1A2 inhibition - 0.8185 81.85%
CYP2C8 inhibition - 0.5854 58.54%
CYP inhibitory promiscuity - 0.6171 61.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Warning 0.4984 49.84%
Eye corrosion - 0.7992 79.92%
Eye irritation - 0.5562 55.62%
Skin irritation + 0.5405 54.05%
Skin corrosion - 0.9888 98.88%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6911 69.11%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6321 63.21%
skin sensitisation + 0.9059 90.59%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.5089 50.89%
Acute Oral Toxicity (c) III 0.8388 83.88%
Estrogen receptor binding - 0.8017 80.17%
Androgen receptor binding - 0.5922 59.22%
Thyroid receptor binding - 0.5637 56.37%
Glucocorticoid receptor binding + 0.5843 58.43%
Aromatase binding - 0.5491 54.91%
PPAR gamma + 0.6698 66.98%
Honey bee toxicity - 0.8418 84.18%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 1.0000 100.00%

Targets

Top

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 97.98% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.20% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.91% 97.25%
CHEMBL233 P35372 Mu opioid receptor 91.33% 97.93%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.75% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.28% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 88.90% 91.49%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 85.10% 95.50%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.34% 100.00%
CHEMBL1937 Q92769 Histone deacetylase 2 83.35% 94.75%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 82.90% 82.05%
CHEMBL325 Q13547 Histone deacetylase 1 80.56% 95.92%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 80.54% 97.50%

Plants that contains it

Top
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.
Bellardia trixago

Cross-Links

Top
PubChem 162851587
LOTUS LTS0036120
wikiData Q105137088