(2E,6E)-3,7,11-trimethyl-10-tritiododeca-2,6,10-trienal

Details

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Internal ID 52ce4be2-5880-4fc2-8c63-6a02e546c778
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2E,6E)-3,7,11-trimethyl-10-tritiododeca-2,6,10-trienal
SMILES (Canonical) CC(=CCCC(=CCCC(=CC=O)C)C)C
SMILES (Isomeric) [3H]C(=C(C)C)CC/C(=C/CC/C(=C/C=O)/C)/C
InChI InChI=1S/C15H24O/c1-13(2)7-5-8-14(3)9-6-10-15(4)11-12-16/h7,9,11-12H,5-6,8,10H2,1-4H3/b14-9+,15-11+/i7T
InChI Key YHRUHBBTQZKMEX-HGWNXUHISA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 222.36 g/mol
Exact Mass 222.190939634 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.60
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2E,6E)-3,7,11-trimethyl-10-tritiododeca-2,6,10-trienal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9931 99.31%
Caco-2 + 0.8276 82.76%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Nucleus 0.5313 53.13%
OATP2B1 inhibitior - 0.8566 85.66%
OATP1B1 inhibitior + 0.8984 89.84%
OATP1B3 inhibitior + 0.9193 91.93%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.5947 59.47%
P-glycoprotein inhibitior - 0.9380 93.80%
P-glycoprotein substrate - 0.8884 88.84%
CYP3A4 substrate - 0.5480 54.80%
CYP2C9 substrate + 0.5960 59.60%
CYP2D6 substrate - 0.8615 86.15%
CYP3A4 inhibition - 0.9808 98.08%
CYP2C9 inhibition - 0.9026 90.26%
CYP2C19 inhibition - 0.9236 92.36%
CYP2D6 inhibition - 0.9630 96.30%
CYP1A2 inhibition - 0.6663 66.63%
CYP2C8 inhibition - 0.9284 92.84%
CYP inhibitory promiscuity - 0.7472 74.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.5749 57.49%
Eye corrosion + 0.7826 78.26%
Eye irritation - 0.5163 51.63%
Skin irritation + 0.8885 88.85%
Skin corrosion - 0.8908 89.08%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6571 65.71%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation + 0.9506 95.06%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.6932 69.32%
Acute Oral Toxicity (c) III 0.7371 73.71%
Estrogen receptor binding - 0.8487 84.87%
Androgen receptor binding - 0.7279 72.79%
Thyroid receptor binding - 0.6367 63.67%
Glucocorticoid receptor binding - 0.5453 54.53%
Aromatase binding - 0.7502 75.02%
PPAR gamma + 0.5209 52.09%
Honey bee toxicity - 0.8708 87.08%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9839 98.39%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.15% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.13% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 87.22% 94.73%
CHEMBL2581 P07339 Cathepsin D 85.09% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.92% 99.17%

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.
Lonicera japonica
Rhodiola crenulata

Cross-Links

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PubChem 10537023
NPASS NPC144249