(3S,6E,9E)-3,7,11-trimethyldodeca-1,6,9,11-tetraen-3-ol

Details

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Internal ID 8d92474b-46a1-494f-b4a9-10bca11073e9
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (3S,6E,9E)-3,7,11-trimethyldodeca-1,6,9,11-tetraen-3-ol
SMILES (Canonical) CC(=C)C=CCC(=CCCC(C)(C=C)O)C
SMILES (Isomeric) CC(=C)/C=C/C/C(=C/CC[C@@](C)(C=C)O)/C
InChI InChI=1S/C15H24O/c1-6-15(5,16)12-8-11-14(4)10-7-9-13(2)3/h6-7,9,11,16H,1-2,8,10,12H2,3-5H3/b9-7+,14-11+/t15-/m1/s1
InChI Key UNWOAULNQCFIRQ-ARUOWJMMSA-N
Popularity 0 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 4.70
Atomic LogP (AlogP) 4.17
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S,6E,9E)-3,7,11-trimethyldodeca-1,6,9,11-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 + 0.9903 99.03%
Caco-2 + 0.8029 80.29%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.4787 47.87%
OATP2B1 inhibitior - 0.8560 85.60%
OATP1B1 inhibitior + 0.9051 90.51%
OATP1B3 inhibitior + 0.9488 94.88%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6600 66.00%
P-glycoprotein inhibitior - 0.9672 96.72%
P-glycoprotein substrate - 0.8910 89.10%
CYP3A4 substrate - 0.5117 51.17%
CYP2C9 substrate - 0.6141 61.41%
CYP2D6 substrate - 0.7761 77.61%
CYP3A4 inhibition - 0.8327 83.27%
CYP2C9 inhibition - 0.8121 81.21%
CYP2C19 inhibition - 0.8459 84.59%
CYP2D6 inhibition - 0.9451 94.51%
CYP1A2 inhibition - 0.6497 64.97%
CYP2C8 inhibition - 0.8011 80.11%
CYP inhibitory promiscuity - 0.8653 86.53%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.6488 64.88%
Eye corrosion - 0.8062 80.62%
Eye irritation + 0.8939 89.39%
Skin irritation + 0.6732 67.32%
Skin corrosion - 0.9752 97.52%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4446 44.46%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5674 56.74%
skin sensitisation + 0.8759 87.59%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.8830 88.30%
Mitochondrial toxicity - 0.8071 80.71%
Nephrotoxicity + 0.6194 61.94%
Acute Oral Toxicity (c) III 0.9106 91.06%
Estrogen receptor binding - 0.8580 85.80%
Androgen receptor binding - 0.8369 83.69%
Thyroid receptor binding - 0.6871 68.71%
Glucocorticoid receptor binding - 0.4934 49.34%
Aromatase binding - 0.6432 64.32%
PPAR gamma + 0.5978 59.78%
Honey bee toxicity - 0.8043 80.43%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9164 91.64%

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
CHEMBL3401 O75469 Pregnane X receptor 89.94% 94.73%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 87.00% 90.93%
CHEMBL1977 P11473 Vitamin D receptor 84.33% 99.43%
CHEMBL2885 P07451 Carbonic anhydrase III 83.00% 87.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.15% 96.95%

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.
Fokienia hodginsii

Cross-Links

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PubChem 23649314
LOTUS LTS0199440
wikiData Q105276177