22-Hydroxy-1-(3-hydroxypiperidin-1-yl)docosa-2,4-dien-1-one

Details

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Internal ID 9ac54118-4d68-4357-b9ea-0153d87e1eac
Taxonomy Organoheterocyclic compounds > Piperidines > N-acylpiperidines
IUPAC Name 22-hydroxy-1-(3-hydroxypiperidin-1-yl)docosa-2,4-dien-1-one
SMILES (Canonical) C1CC(CN(C1)C(=O)C=CC=CCCCCCCCCCCCCCCCCCO)O
SMILES (Isomeric) C1CC(CN(C1)C(=O)C=CC=CCCCCCCCCCCCCCCCCCO)O
InChI InChI=1S/C27H49NO3/c29-24-19-17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-18-22-27(31)28-23-20-21-26(30)25-28/h14,16,18,22,26,29-30H,1-13,15,17,19-21,23-25H2
InChI Key NRAYLTGUCYPLFK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H49NO3
Molecular Weight 435.70 g/mol
Exact Mass 435.37124443 g/mol
Topological Polar Surface Area (TPSA) 60.80 Ų
XlogP 8.00
Atomic LogP (AlogP) 6.32
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 19

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 22-Hydroxy-1-(3-hydroxypiperidin-1-yl)docosa-2,4-dien-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9594 95.94%
Caco-2 - 0.8468 84.68%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.8199 81.99%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior + 0.9182 91.82%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior + 0.7045 70.45%
P-glycoprotein inhibitior - 0.6091 60.91%
P-glycoprotein substrate - 0.7104 71.04%
CYP3A4 substrate + 0.5442 54.42%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8623 86.23%
CYP3A4 inhibition - 0.9655 96.55%
CYP2C9 inhibition - 0.9390 93.90%
CYP2C19 inhibition - 0.8863 88.63%
CYP2D6 inhibition - 0.9477 94.77%
CYP1A2 inhibition - 0.9281 92.81%
CYP2C8 inhibition - 0.8693 86.93%
CYP inhibitory promiscuity - 0.9706 97.06%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6267 62.67%
Eye corrosion - 0.9620 96.20%
Eye irritation - 0.7807 78.07%
Skin irritation - 0.6503 65.03%
Skin corrosion - 0.8825 88.25%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8287 82.87%
Micronuclear - 0.5500 55.00%
Hepatotoxicity + 0.5532 55.32%
skin sensitisation - 0.9083 90.83%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.6491 64.91%
Acute Oral Toxicity (c) III 0.5216 52.16%
Estrogen receptor binding + 0.6715 67.15%
Androgen receptor binding - 0.5855 58.55%
Thyroid receptor binding + 0.5523 55.23%
Glucocorticoid receptor binding + 0.6011 60.11%
Aromatase binding - 0.6134 61.34%
PPAR gamma + 0.6184 61.84%
Honey bee toxicity - 0.9383 93.83%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.6476 64.76%
Fish aquatic toxicity - 0.9761 97.61%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.00% 96.09%
CHEMBL4394 Q9NYA1 Sphingosine kinase 1 91.69% 96.03%
CHEMBL4588 P22894 Matrix metalloproteinase 8 91.54% 94.66%
CHEMBL230 P35354 Cyclooxygenase-2 90.06% 89.63%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 89.58% 97.47%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.24% 99.17%
CHEMBL2581 P07339 Cathepsin D 87.93% 98.95%
CHEMBL3023 Q9NRA0 Sphingosine kinase 2 87.81% 95.61%
CHEMBL237 P41145 Kappa opioid receptor 86.76% 98.10%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.54% 92.94%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 85.87% 100.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 85.71% 95.50%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 85.59% 98.33%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 85.31% 98.46%
CHEMBL3105 P09874 Poly [ADP-ribose] polymerase-1 85.27% 93.90%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 84.91% 97.34%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 84.28% 82.05%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.47% 95.89%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 83.38% 92.95%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 83.37% 95.27%
CHEMBL5255 O00206 Toll-like receptor 4 81.11% 92.50%
CHEMBL5103 Q969S8 Histone deacetylase 10 80.14% 90.08%
CHEMBL1744525 P43490 Nicotinamide phosphoribosyltransferase 80.00% 96.25%

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.
Clusia columnaris
Clusia sandiensis
Haloxylon salicornicum

Cross-Links

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PubChem 72967383
LOTUS LTS0107029
wikiData Q104399757