10-Hydroxy-2,6,10-trimethyldodeca-2,6,11-trienal

Details

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Internal ID 1508b74a-c6aa-4059-a0e8-67947b59b643
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 10-hydroxy-2,6,10-trimethyldodeca-2,6,11-trienal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O2/c1-5-15(4,17)11-7-10-13(2)8-6-9-14(3)12-16/h5,9-10,12,17H,1,6-8,11H2,2-4H3
InChI Key YFRYWBKXJHBSNO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O2
Molecular Weight 236.35 g/mol
Exact Mass 236.177630004 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.58
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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10-HYDROXY-2,6,10-TRIMETHYLDODECA-2,6,11-TRIENAL
DTXSID80786855

2D Structure

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2D Structure of 10-Hydroxy-2,6,10-trimethyldodeca-2,6,11-trienal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9944 99.44%
Caco-2 + 0.6572 65.72%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.5434 54.34%
OATP2B1 inhibitior - 0.8536 85.36%
OATP1B1 inhibitior + 0.9239 92.39%
OATP1B3 inhibitior + 0.9393 93.93%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.4822 48.22%
P-glycoprotein inhibitior - 0.9577 95.77%
P-glycoprotein substrate - 0.9026 90.26%
CYP3A4 substrate + 0.5158 51.58%
CYP2C9 substrate - 0.8119 81.19%
CYP2D6 substrate - 0.8483 84.83%
CYP3A4 inhibition - 0.7759 77.59%
CYP2C9 inhibition - 0.8205 82.05%
CYP2C19 inhibition - 0.8647 86.47%
CYP2D6 inhibition - 0.9401 94.01%
CYP1A2 inhibition - 0.5884 58.84%
CYP2C8 inhibition - 0.8781 87.81%
CYP inhibitory promiscuity - 0.9130 91.30%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Non-required 0.6569 65.69%
Eye corrosion - 0.7606 76.06%
Eye irritation + 0.9152 91.52%
Skin irritation + 0.6737 67.37%
Skin corrosion - 0.9696 96.96%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5601 56.01%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5799 57.99%
skin sensitisation + 0.8215 82.15%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.8028 80.28%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.5574 55.74%
Acute Oral Toxicity (c) III 0.8957 89.57%
Estrogen receptor binding - 0.7642 76.42%
Androgen receptor binding - 0.8398 83.98%
Thyroid receptor binding - 0.6052 60.52%
Glucocorticoid receptor binding - 0.4845 48.45%
Aromatase binding - 0.6378 63.78%
PPAR gamma + 0.7255 72.55%
Honey bee toxicity - 0.7898 78.98%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9244 92.44%

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 90.93% 94.73%
CHEMBL2581 P07339 Cathepsin D 88.52% 98.95%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 86.70% 90.93%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.52% 89.34%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.14% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.51% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.07% 97.25%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 81.28% 92.08%

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.
Arctotis aspera

Cross-Links

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PubChem 71363283
LOTUS LTS0261716
wikiData Q82753323