9-Cycloneren-3,7,11-triol

Details

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Internal ID bc733096-77f9-470b-b3d3-780abb996396
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (E,6R)-6-[(1R,2S,3R)-3-hydroxy-2,3-dimethylcyclopentyl]-2-methylhept-3-ene-2,6-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H28O3/c1-11-12(7-10-14(11,4)17)15(5,18)9-6-8-13(2,3)16/h6,8,11-12,16-18H,7,9-10H2,1-5H3/b8-6+/t11-,12+,14+,15+/m0/s1
InChI Key GXIOKIVWOMSPIP-CKUBQHFVSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H28O3
Molecular Weight 256.38 g/mol
Exact Mass 256.20384475 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.25
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 9-Cycloneren-3,7,11-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9904 99.04%
Caco-2 + 0.7126 71.26%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6937 69.37%
OATP2B1 inhibitior - 0.8513 85.13%
OATP1B1 inhibitior + 0.8975 89.75%
OATP1B3 inhibitior + 0.9576 95.76%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.6216 62.16%
P-glycoprotein inhibitior - 0.9241 92.41%
P-glycoprotein substrate - 0.8383 83.83%
CYP3A4 substrate + 0.5366 53.66%
CYP2C9 substrate - 0.7759 77.59%
CYP2D6 substrate - 0.7764 77.64%
CYP3A4 inhibition - 0.8732 87.32%
CYP2C9 inhibition - 0.8787 87.87%
CYP2C19 inhibition - 0.8658 86.58%
CYP2D6 inhibition - 0.9540 95.40%
CYP1A2 inhibition - 0.8524 85.24%
CYP2C8 inhibition - 0.8020 80.20%
CYP inhibitory promiscuity - 0.8599 85.99%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9028 90.28%
Carcinogenicity (trinary) Non-required 0.7093 70.93%
Eye corrosion - 0.9676 96.76%
Eye irritation - 0.8644 86.44%
Skin irritation + 0.5493 54.93%
Skin corrosion - 0.9538 95.38%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7170 71.70%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5027 50.27%
skin sensitisation + 0.6821 68.21%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.7064 70.64%
Acute Oral Toxicity (c) I 0.3939 39.39%
Estrogen receptor binding - 0.5905 59.05%
Androgen receptor binding - 0.7541 75.41%
Thyroid receptor binding + 0.5413 54.13%
Glucocorticoid receptor binding + 0.5576 55.76%
Aromatase binding - 0.5544 55.44%
PPAR gamma - 0.7557 75.57%
Honey bee toxicity - 0.9067 90.67%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9470 94.70%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.87% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.25% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.20% 96.09%
CHEMBL206 P03372 Estrogen receptor alpha 83.01% 97.64%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.43% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.41% 100.00%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 80.81% 100.00%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 80.63% 91.03%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.45% 95.89%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139590988
LOTUS LTS0035968
wikiData Q105023079