12-Hydroxy-6,10-dimethyl-2-(4-methylpent-3-enyl)dodeca-2,6,10-trienal

Details

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Internal ID bda4e7d1-34c6-440d-9c2f-b06b0c9f53bc
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name 12-hydroxy-6,10-dimethyl-2-(4-methylpent-3-enyl)dodeca-2,6,10-trienal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32O2/c1-17(2)8-5-12-20(16-22)13-7-11-18(3)9-6-10-19(4)14-15-21/h8-9,13-14,16,21H,5-7,10-12,15H2,1-4H3
InChI Key BVHBRLCYRXLBJQ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O2
Molecular Weight 304.50 g/mol
Exact Mass 304.240230259 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 5.20
Atomic LogP (AlogP) 5.30
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 12-Hydroxy-6,10-dimethyl-2-(4-methylpent-3-enyl)dodeca-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 + 0.9898 98.98%
Caco-2 + 0.7855 78.55%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.4582 45.82%
OATP2B1 inhibitior - 0.8539 85.39%
OATP1B1 inhibitior + 0.9145 91.45%
OATP1B3 inhibitior + 0.9158 91.58%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.8730 87.30%
P-glycoprotein inhibitior - 0.6857 68.57%
P-glycoprotein substrate - 0.9389 93.89%
CYP3A4 substrate - 0.5571 55.71%
CYP2C9 substrate - 0.8129 81.29%
CYP2D6 substrate - 0.8429 84.29%
CYP3A4 inhibition - 0.9171 91.71%
CYP2C9 inhibition - 0.8568 85.68%
CYP2C19 inhibition - 0.8851 88.51%
CYP2D6 inhibition - 0.9058 90.58%
CYP1A2 inhibition - 0.8192 81.92%
CYP2C8 inhibition - 0.9427 94.27%
CYP inhibitory promiscuity - 0.8221 82.21%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6400 64.00%
Carcinogenicity (trinary) Non-required 0.6821 68.21%
Eye corrosion + 0.5379 53.79%
Eye irritation + 0.6892 68.92%
Skin irritation + 0.7779 77.79%
Skin corrosion - 0.9509 95.09%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4002 40.02%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.7250 72.50%
skin sensitisation + 0.8309 83.09%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.9368 93.68%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.7094 70.94%
Acute Oral Toxicity (c) III 0.7642 76.42%
Estrogen receptor binding - 0.6590 65.90%
Androgen receptor binding - 0.8254 82.54%
Thyroid receptor binding + 0.6985 69.85%
Glucocorticoid receptor binding - 0.5698 56.98%
Aromatase binding + 0.5554 55.54%
PPAR gamma + 0.8181 81.81%
Honey bee toxicity - 0.9396 93.96%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9551 95.51%

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 93.53% 92.08%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 84.39% 91.24%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.88% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 82.50% 94.73%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.34% 89.34%

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.
Calocedrus formosana
Croton kerrii

Cross-Links

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PubChem 72751626
LOTUS LTS0125133
wikiData Q104946551