Nerylgeraniol-18-oic acid

Details

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Internal ID 7a44e3b8-a20a-41c7-8df4-0ee461e56473
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name (2E,6E,10E)-12-hydroxy-6,10-dimethyl-2-(4-methylpent-3-enyl)dodeca-2,6,10-trienoic acid
SMILES (Canonical) CC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C(=O)O)C
SMILES (Isomeric) CC(=CCC/C(=C\CC/C(=C/CC/C(=C/CO)/C)/C)/C(=O)O)C
InChI InChI=1S/C20H32O3/c1-16(2)8-5-12-19(20(22)23)13-7-11-17(3)9-6-10-18(4)14-15-21/h8-9,13-14,21H,5-7,10-12,15H2,1-4H3,(H,22,23)/b17-9+,18-14+,19-13+
InChI Key USXGDFAHMRCBBX-PFZXPCEQSA-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 5.30
Atomic LogP (AlogP) 5.19
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 11

Synonyms

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AKOS040736068
126794-69-2

2D Structure

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2D Structure of Nerylgeraniol-18-oic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9820 98.20%
Caco-2 + 0.6943 69.43%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.6916 69.16%
OATP2B1 inhibitior - 0.8531 85.31%
OATP1B1 inhibitior + 0.9189 91.89%
OATP1B3 inhibitior + 0.9029 90.29%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.8628 86.28%
P-glycoprotein inhibitior - 0.7324 73.24%
P-glycoprotein substrate - 0.9570 95.70%
CYP3A4 substrate - 0.5760 57.60%
CYP2C9 substrate - 0.5754 57.54%
CYP2D6 substrate - 0.9111 91.11%
CYP3A4 inhibition - 0.8419 84.19%
CYP2C9 inhibition - 0.7712 77.12%
CYP2C19 inhibition - 0.8953 89.53%
CYP2D6 inhibition - 0.8983 89.83%
CYP1A2 inhibition - 0.8071 80.71%
CYP2C8 inhibition - 0.9579 95.79%
CYP inhibitory promiscuity - 0.8239 82.39%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7023 70.23%
Carcinogenicity (trinary) Non-required 0.6721 67.21%
Eye corrosion - 0.8071 80.71%
Eye irritation + 0.6604 66.04%
Skin irritation - 0.6399 63.99%
Skin corrosion - 0.9806 98.06%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5332 53.32%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.8625 86.25%
skin sensitisation + 0.5548 55.48%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.8642 86.42%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.6000 60.00%
Acute Oral Toxicity (c) IV 0.6918 69.18%
Estrogen receptor binding - 0.5824 58.24%
Androgen receptor binding - 0.6852 68.52%
Thyroid receptor binding + 0.6576 65.76%
Glucocorticoid receptor binding - 0.5113 51.13%
Aromatase binding + 0.5224 52.24%
PPAR gamma + 0.8692 86.92%
Honey bee toxicity - 0.9518 95.18%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity + 0.9877 98.77%

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 91.87% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.92% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.72% 96.09%
CHEMBL2581 P07339 Cathepsin D 84.05% 98.95%
CHEMBL340 P08684 Cytochrome P450 3A4 80.40% 91.19%

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.
Diplostephium ericoides
Glaucium oxylobum

Cross-Links

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PubChem 11186287
NPASS NPC127654
LOTUS LTS0171533
wikiData Q104399931