8-epi-Halosaline

Details

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Internal ID 161eb972-e6f4-4744-bde0-0eb94c5f5ed9
Taxonomy Organoheterocyclic compounds > Piperidines
IUPAC Name (2R)-1-[(2S)-piperidin-2-yl]pentan-2-ol
SMILES (Canonical) CCCC(CC1CCCCN1)O
SMILES (Isomeric) CCC[C@H](C[C@@H]1CCCCN1)O
InChI InChI=1S/C10H21NO/c1-2-5-10(12)8-9-6-3-4-7-11-9/h9-12H,2-8H2,1H3/t9-,10+/m0/s1
InChI Key UNJGJWVJJMZDOT-VHSXEESVSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C10H21NO
Molecular Weight 171.28 g/mol
Exact Mass 171.162314293 g/mol
Topological Polar Surface Area (TPSA) 32.30 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.68
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8-epi-Halosaline

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9646 96.46%
Caco-2 + 0.7729 77.29%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.6670 66.70%
OATP2B1 inhibitior - 0.8474 84.74%
OATP1B1 inhibitior + 0.9573 95.73%
OATP1B3 inhibitior + 0.9443 94.43%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.8879 88.79%
P-glycoprotein inhibitior - 0.9693 96.93%
P-glycoprotein substrate - 0.7307 73.07%
CYP3A4 substrate - 0.6340 63.40%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.5555 55.55%
CYP3A4 inhibition - 0.9778 97.78%
CYP2C9 inhibition - 0.8964 89.64%
CYP2C19 inhibition - 0.9432 94.32%
CYP2D6 inhibition - 0.6484 64.84%
CYP1A2 inhibition - 0.8186 81.86%
CYP2C8 inhibition - 0.9551 95.51%
CYP inhibitory promiscuity - 0.9576 95.76%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6917 69.17%
Eye corrosion + 0.5222 52.22%
Eye irritation + 0.7441 74.41%
Skin irritation - 0.5673 56.73%
Skin corrosion - 0.5624 56.24%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6635 66.35%
Micronuclear - 0.7800 78.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.7808 78.08%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.7266 72.66%
Acute Oral Toxicity (c) III 0.7388 73.88%
Estrogen receptor binding - 0.8320 83.20%
Androgen receptor binding - 0.8008 80.08%
Thyroid receptor binding - 0.7427 74.27%
Glucocorticoid receptor binding - 0.7353 73.53%
Aromatase binding - 0.8707 87.07%
PPAR gamma - 0.8663 86.63%
Honey bee toxicity - 0.9835 98.35%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity - 0.9499 94.99%

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 97.03% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.91% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.76% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.24% 97.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.90% 93.56%
CHEMBL237 P41145 Kappa opioid receptor 89.01% 98.10%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.46% 94.45%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 86.91% 92.88%
CHEMBL213 P08588 Beta-1 adrenergic receptor 86.44% 95.56%
CHEMBL238 Q01959 Dopamine transporter 84.43% 95.88%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.94% 96.95%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 83.93% 100.00%
CHEMBL206 P03372 Estrogen receptor alpha 82.56% 97.64%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 82.40% 98.33%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.01% 93.03%
CHEMBL4105838 Q96GG9 DCN1-like protein 1 81.95% 95.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.89% 100.00%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 80.30% 97.50%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.28% 92.62%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.14% 95.50%

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.
Andrachne aspera

Cross-Links

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PubChem 11355750
LOTUS LTS0024333
wikiData Q105276003