(3S,4E,6E)-3,7,11-trimethyldodeca-1,4,6,10-tetraen-3-ol

Details

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Internal ID f37352fd-904a-43ce-8f00-b3760bc4a471
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (3S,4E,6E)-3,7,11-trimethyldodeca-1,4,6,10-tetraen-3-ol
SMILES (Canonical) CC(=CCCC(=CC=CC(C)(C=C)O)C)C
SMILES (Isomeric) CC(=CCC/C(=C/C=C/[C@](C)(C=C)O)/C)C
InChI InChI=1S/C15H24O/c1-6-15(5,16)12-8-11-14(4)10-7-9-13(2)3/h6,8-9,11-12,16H,1,7,10H2,2-5H3/b12-8+,14-11+/t15-/m0/s1
InChI Key UIMSQVVHHIUQOZ-QMHMUBQMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.17
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S,4E,6E)-3,7,11-trimethyldodeca-1,4,6,10-tetraen-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9835 98.35%
Caco-2 + 0.9414 94.14%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Nucleus 0.4733 47.33%
OATP2B1 inhibitior - 0.8624 86.24%
OATP1B1 inhibitior + 0.9143 91.43%
OATP1B3 inhibitior + 0.9076 90.76%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.5748 57.48%
P-glycoprotein inhibitior - 0.9659 96.59%
P-glycoprotein substrate - 0.9346 93.46%
CYP3A4 substrate - 0.5301 53.01%
CYP2C9 substrate - 0.6141 61.41%
CYP2D6 substrate - 0.7761 77.61%
CYP3A4 inhibition - 0.8723 87.23%
CYP2C9 inhibition - 0.8510 85.10%
CYP2C19 inhibition - 0.7993 79.93%
CYP2D6 inhibition - 0.9334 93.34%
CYP1A2 inhibition - 0.8011 80.11%
CYP2C8 inhibition - 0.9037 90.37%
CYP inhibitory promiscuity - 0.7627 76.27%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.5300 53.00%
Carcinogenicity (trinary) Non-required 0.6091 60.91%
Eye corrosion + 0.4723 47.23%
Eye irritation + 0.9052 90.52%
Skin irritation + 0.9153 91.53%
Skin corrosion - 0.8759 87.59%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4742 47.42%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation + 0.9024 90.24%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.5691 56.91%
Acute Oral Toxicity (c) III 0.8434 84.34%
Estrogen receptor binding - 0.8614 86.14%
Androgen receptor binding - 0.8093 80.93%
Thyroid receptor binding - 0.6564 65.64%
Glucocorticoid receptor binding - 0.5564 55.64%
Aromatase binding - 0.7188 71.88%
PPAR gamma + 0.5506 55.06%
Honey bee toxicity - 0.8097 80.97%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.8624 86.24%

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 87.64% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 87.52% 94.73%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.69% 92.08%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.59% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.32% 91.11%
CHEMBL1977 P11473 Vitamin D receptor 83.33% 99.43%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.96% 96.09%

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.
Austroeupatorium chaparense
Brickellia californica

Cross-Links

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PubChem 162945410
LOTUS LTS0082878
wikiData Q105273486