7-Hydroxy-1-(2-pyridin-3-ylpyrrolidin-1-yl)octan-1-one

Details

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Internal ID b060cba2-e119-443d-b663-e693d5eeaca6
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Pyrrolidinylpyridines
IUPAC Name 7-hydroxy-1-(2-pyridin-3-ylpyrrolidin-1-yl)octan-1-one
SMILES (Canonical) CC(CCCCCC(=O)N1CCCC1C2=CN=CC=C2)O
SMILES (Isomeric) CC(CCCCCC(=O)N1CCCC1C2=CN=CC=C2)O
InChI InChI=1S/C17H26N2O2/c1-14(20)7-3-2-4-10-17(21)19-12-6-9-16(19)15-8-5-11-18-13-15/h5,8,11,13-14,16,20H,2-4,6-7,9-10,12H2,1H3
InChI Key AAIYOWLBULBBDR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H26N2O2
Molecular Weight 290.40 g/mol
Exact Mass 290.199428076 g/mol
Topological Polar Surface Area (TPSA) 53.40 Ų
XlogP 2.00
Atomic LogP (AlogP) 3.08
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Hydroxy-1-(2-pyridin-3-ylpyrrolidin-1-yl)octan-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 + 0.9912 99.12%
Caco-2 + 0.7033 70.33%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.8260 82.60%
OATP2B1 inhibitior - 0.8586 85.86%
OATP1B1 inhibitior + 0.9403 94.03%
OATP1B3 inhibitior + 0.9373 93.73%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.9372 93.72%
P-glycoprotein inhibitior - 0.8652 86.52%
P-glycoprotein substrate + 0.5094 50.94%
CYP3A4 substrate + 0.5368 53.68%
CYP2C9 substrate - 0.7850 78.50%
CYP2D6 substrate - 0.8225 82.25%
CYP3A4 inhibition - 0.7034 70.34%
CYP2C9 inhibition - 0.8053 80.53%
CYP2C19 inhibition - 0.6997 69.97%
CYP2D6 inhibition - 0.8973 89.73%
CYP1A2 inhibition - 0.8932 89.32%
CYP2C8 inhibition - 0.7803 78.03%
CYP inhibitory promiscuity - 0.7660 76.60%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6788 67.88%
Eye corrosion - 0.9903 99.03%
Eye irritation - 0.9482 94.82%
Skin irritation - 0.7455 74.55%
Skin corrosion - 0.8360 83.60%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4835 48.35%
Micronuclear - 0.5100 51.00%
Hepatotoxicity + 0.6284 62.84%
skin sensitisation - 0.9156 91.56%
Respiratory toxicity + 0.9000 90.00%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.8555 85.55%
Acute Oral Toxicity (c) III 0.5834 58.34%
Estrogen receptor binding + 0.6103 61.03%
Androgen receptor binding - 0.7665 76.65%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.5886 58.86%
Aromatase binding - 0.6604 66.04%
PPAR gamma + 0.6349 63.49%
Honey bee toxicity - 0.9636 96.36%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5976 59.76%
Fish aquatic toxicity - 0.4489 44.89%

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 99.32% 96.09%
CHEMBL2581 P07339 Cathepsin D 98.44% 98.95%
CHEMBL5203 P33316 dUTP pyrophosphatase 93.22% 99.18%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.30% 94.45%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 90.89% 90.71%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 90.00% 98.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.78% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.54% 85.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.26% 95.89%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.15% 93.56%
CHEMBL4040 P28482 MAP kinase ERK2 87.50% 83.82%
CHEMBL1744525 P43490 Nicotinamide phosphoribosyltransferase 87.21% 96.25%
CHEMBL3524 P56524 Histone deacetylase 4 85.01% 92.97%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.60% 95.89%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 83.77% 100.00%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 83.59% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.91% 86.33%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.97% 93.03%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.83% 99.17%
CHEMBL1907589 P17787 Neuronal acetylcholine receptor; alpha4/beta2 80.50% 94.55%
CHEMBL274 P51681 C-C chemokine receptor type 5 80.43% 98.77%

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.
Nicotiana tabacum

Cross-Links

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PubChem 162934667
LOTUS LTS0156407
wikiData Q104907946