18-Oxo-19-hydroxynerylgeraniol

Details

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Internal ID d7df9696-4bbe-4e0f-9b69-6486f1083a37
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name (2E,6Z,10E)-12-hydroxy-6-(hydroxymethyl)-10-methyl-2-(4-methylpent-3-enyl)dodeca-2,6,10-trienal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32O3/c1-17(2)7-4-9-19(15-22)11-6-12-20(16-23)10-5-8-18(3)13-14-21/h7,10-11,13,15,21,23H,4-6,8-9,12,14,16H2,1-3H3/b18-13+,19-11+,20-10-
InChI Key UUFWIQNOFSEUPP-RHGHSNSYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O3
Molecular Weight 320.50 g/mol
Exact Mass 320.23514488 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 4.00
Atomic LogP (AlogP) 4.28
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 18-Oxo-19-hydroxynerylgeraniol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9776 97.76%
Caco-2 + 0.5792 57.92%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.6107 61.07%
OATP2B1 inhibitior - 0.8551 85.51%
OATP1B1 inhibitior + 0.8965 89.65%
OATP1B3 inhibitior + 0.9304 93.04%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.7541 75.41%
BSEP inhibitior + 0.8553 85.53%
P-glycoprotein inhibitior - 0.7354 73.54%
P-glycoprotein substrate - 0.8794 87.94%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8129 81.29%
CYP2D6 substrate - 0.8429 84.29%
CYP3A4 inhibition - 0.8323 83.23%
CYP2C9 inhibition - 0.8160 81.60%
CYP2C19 inhibition - 0.8754 87.54%
CYP2D6 inhibition - 0.8885 88.85%
CYP1A2 inhibition - 0.8283 82.83%
CYP2C8 inhibition - 0.8950 89.50%
CYP inhibitory promiscuity - 0.8543 85.43%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6923 69.23%
Carcinogenicity (trinary) Non-required 0.6633 66.33%
Eye corrosion - 0.7410 74.10%
Eye irritation + 0.5781 57.81%
Skin irritation - 0.6831 68.31%
Skin corrosion - 0.9684 96.84%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5613 56.13%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6875 68.75%
skin sensitisation + 0.6049 60.49%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.8865 88.65%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.7319 73.19%
Acute Oral Toxicity (c) IV 0.7184 71.84%
Estrogen receptor binding + 0.5609 56.09%
Androgen receptor binding - 0.8027 80.27%
Thyroid receptor binding + 0.6630 66.30%
Glucocorticoid receptor binding - 0.5173 51.73%
Aromatase binding + 0.5847 58.47%
PPAR gamma + 0.8413 84.13%
Honey bee toxicity - 0.9180 91.80%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.9709 97.09%

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 87.38% 92.08%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.50% 89.34%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 84.53% 91.24%
CHEMBL3401 O75469 Pregnane X receptor 83.30% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.38% 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.
Vittadinia gracilis

Cross-Links

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PubChem 14138924
LOTUS LTS0007440
wikiData Q105279300