Cycloneran-3,7,11-triol

Details

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Internal ID e534252b-466c-465d-b665-ddfb21e126be
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2-[(1S,2R,3S)-3-hydroxy-2,3-dimethylcyclopentyl]-6-methylheptane-2,6-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H30O3/c1-11-12(7-10-14(11,4)17)15(5,18)9-6-8-13(2,3)16/h11-12,16-18H,6-10H2,1-5H3/t11-,12+,14+,15?/m1/s1
InChI Key VBPRGBNBDPONAI-JNZNFYPTSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H30O3
Molecular Weight 258.40 g/mol
Exact Mass 258.21949481 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.48
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Cycloneran-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 + 0.9879 98.79%
Caco-2 + 0.7711 77.11%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7138 71.38%
OATP2B1 inhibitior - 0.8481 84.81%
OATP1B1 inhibitior + 0.9266 92.66%
OATP1B3 inhibitior + 0.9625 96.25%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6956 69.56%
P-glycoprotein inhibitior - 0.9055 90.55%
P-glycoprotein substrate - 0.7411 74.11%
CYP3A4 substrate + 0.5221 52.21%
CYP2C9 substrate - 0.6084 60.84%
CYP2D6 substrate - 0.7417 74.17%
CYP3A4 inhibition - 0.9131 91.31%
CYP2C9 inhibition - 0.8546 85.46%
CYP2C19 inhibition - 0.9155 91.55%
CYP2D6 inhibition - 0.9582 95.82%
CYP1A2 inhibition - 0.8793 87.93%
CYP2C8 inhibition - 0.8325 83.25%
CYP inhibitory promiscuity - 0.9203 92.03%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.7324 73.24%
Eye corrosion - 0.9525 95.25%
Eye irritation - 0.7094 70.94%
Skin irritation + 0.5134 51.34%
Skin corrosion - 0.9456 94.56%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7552 75.52%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6640 66.40%
skin sensitisation + 0.6736 67.36%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.7768 77.68%
Acute Oral Toxicity (c) III 0.6076 60.76%
Estrogen receptor binding - 0.5054 50.54%
Androgen receptor binding - 0.6725 67.25%
Thyroid receptor binding + 0.5464 54.64%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding - 0.5128 51.28%
PPAR gamma - 0.8079 80.79%
Honey bee toxicity - 0.9383 93.83%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.8821 88.21%

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 98.51% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.30% 96.09%
CHEMBL206 P03372 Estrogen receptor alpha 90.85% 97.64%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.53% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.64% 97.09%
CHEMBL2996 Q05655 Protein kinase C delta 88.09% 97.79%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 84.75% 89.05%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 84.64% 91.03%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.50% 100.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.83% 100.00%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 82.71% 100.00%
CHEMBL2581 P07339 Cathepsin D 81.70% 98.95%
CHEMBL226 P30542 Adenosine A1 receptor 81.20% 95.93%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.60% 92.94%
CHEMBL3045 P05771 Protein kinase C beta 80.45% 97.63%

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 146682955
LOTUS LTS0190081
wikiData Q105283407