(3E,5E,7S,8E)-3,7,11-trimethyldodeca-1,3,5,8,10-pentaene

Details

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Internal ID c82f8c6e-3168-4844-8076-3749a533f1dc
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (3E,5E,7S,8E)-3,7,11-trimethyldodeca-1,3,5,8,10-pentaene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22/c1-6-14(4)10-8-12-15(5)11-7-9-13(2)3/h6-12,15H,1H2,2-5H3/b11-7+,12-8+,14-10+/t15-/m0/s1
InChI Key DSZALOUXXLZEOV-UXKFGHTFSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22
Molecular Weight 202.33 g/mol
Exact Mass 202.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.90
Atomic LogP (AlogP) 4.83
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3E,5E,7S,8E)-3,7,11-trimethyldodeca-1,3,5,8,10-pentaene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9890 98.90%
Caco-2 + 0.9253 92.53%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Lysosomes 0.4778 47.78%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9204 92.04%
OATP1B3 inhibitior + 0.9530 95.30%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7181 71.81%
P-glycoprotein inhibitior - 0.9533 95.33%
P-glycoprotein substrate - 0.9396 93.96%
CYP3A4 substrate - 0.6170 61.70%
CYP2C9 substrate - 0.6141 61.41%
CYP2D6 substrate - 0.8047 80.47%
CYP3A4 inhibition - 0.9124 91.24%
CYP2C9 inhibition - 0.8899 88.99%
CYP2C19 inhibition - 0.8666 86.66%
CYP2D6 inhibition - 0.9303 93.03%
CYP1A2 inhibition - 0.8596 85.96%
CYP2C8 inhibition - 0.9786 97.86%
CYP inhibitory promiscuity - 0.7220 72.20%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6783 67.83%
Carcinogenicity (trinary) Warning 0.5909 59.09%
Eye corrosion + 0.9590 95.90%
Eye irritation + 0.9636 96.36%
Skin irritation + 0.7427 74.27%
Skin corrosion - 0.9684 96.84%
Ames mutagenesis - 0.7291 72.91%
Human Ether-a-go-go-Related Gene inhibition - 0.4716 47.16%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5557 55.57%
skin sensitisation + 0.8744 87.44%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.6214 62.14%
Nephrotoxicity + 0.5529 55.29%
Acute Oral Toxicity (c) III 0.5588 55.88%
Estrogen receptor binding - 0.6776 67.76%
Androgen receptor binding - 0.9287 92.87%
Thyroid receptor binding - 0.7218 72.18%
Glucocorticoid receptor binding - 0.7367 73.67%
Aromatase binding - 0.5195 51.95%
PPAR gamma - 0.7373 73.73%
Honey bee toxicity - 0.7428 74.28%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.8100 81.00%
Fish aquatic toxicity + 0.9366 93.66%

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 96.48% 83.82%
CHEMBL2581 P07339 Cathepsin D 87.54% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.86% 96.09%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 81.61% 82.05%
CHEMBL226 P30542 Adenosine A1 receptor 80.91% 95.93%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.70% 85.14%
CHEMBL2885 P07451 Carbonic anhydrase III 80.33% 87.45%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162885436
LOTUS LTS0240798
wikiData Q104988133