13-Methyltetradeca-2,9-diene

Details

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Internal ID c1bcb632-5cd9-40fa-811b-8d869f9e8e5d
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Acyclic olefins > Alkadienes
IUPAC Name 13-methyltetradeca-2,9-diene
SMILES (Canonical) CC=CCCCCCC=CCCC(C)C
SMILES (Isomeric) CC=CCCCCCC=CCCC(C)C
InChI InChI=1S/C15H28/c1-4-5-6-7-8-9-10-11-12-13-14-15(2)3/h4-5,11-12,15H,6-10,13-14H2,1-3H3
InChI Key SZHOGKYPRQCASK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H28
Molecular Weight 208.38 g/mol
Exact Mass 208.219100893 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.30
Atomic LogP (AlogP) 5.51
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 13-Methyltetradeca-2,9-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9899 98.99%
Caco-2 + 0.8769 87.69%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Nucleus 0.3537 35.37%
OATP2B1 inhibitior - 0.8531 85.31%
OATP1B1 inhibitior + 0.8560 85.60%
OATP1B3 inhibitior + 0.9392 93.92%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6429 64.29%
P-glycoprotein inhibitior - 0.9075 90.75%
P-glycoprotein substrate - 0.8829 88.29%
CYP3A4 substrate - 0.6220 62.20%
CYP2C9 substrate - 0.8071 80.71%
CYP2D6 substrate - 0.7561 75.61%
CYP3A4 inhibition - 0.9848 98.48%
CYP2C9 inhibition - 0.9294 92.94%
CYP2C19 inhibition - 0.9385 93.85%
CYP2D6 inhibition - 0.9585 95.85%
CYP1A2 inhibition - 0.6992 69.92%
CYP2C8 inhibition - 0.9821 98.21%
CYP inhibitory promiscuity - 0.8115 81.15%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.5503 55.03%
Eye corrosion + 0.9616 96.16%
Eye irritation + 0.8300 83.00%
Skin irritation + 0.8930 89.30%
Skin corrosion - 0.9755 97.55%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4553 45.53%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5467 54.67%
skin sensitisation + 0.9600 96.00%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.7007 70.07%
Acute Oral Toxicity (c) III 0.8572 85.72%
Estrogen receptor binding - 0.8707 87.07%
Androgen receptor binding - 0.8381 83.81%
Thyroid receptor binding + 0.5641 56.41%
Glucocorticoid receptor binding - 0.6505 65.05%
Aromatase binding - 0.7712 77.12%
PPAR gamma - 0.5301 53.01%
Honey bee toxicity - 0.9409 94.09%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.9880 98.80%

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
CHEMBL2581 P07339 Cathepsin D 91.44% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.08% 99.17%
CHEMBL1907 P15144 Aminopeptidase N 89.73% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.63% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 87.50% 97.29%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 86.23% 96.47%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.85% 92.86%
CHEMBL2885 P07451 Carbonic anhydrase III 83.37% 87.45%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 82.38% 92.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.97% 93.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.22% 96.00%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 80.43% 95.17%

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.
Echinacea angustifolia

Cross-Links

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PubChem 54332465
NPASS NPC252762