2-Dodecanone, 12-(5-hydroxy-1,6-dimethyl-2-piperidinyl)-, (2S-(2alpha,5alpha,6alpha))-

Details

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Internal ID 8dce7559-eac8-4ba3-b9b5-c0750485202f
Taxonomy Alkaloids and derivatives
IUPAC Name 12-[(2S,5S,6S)-5-hydroxy-1,6-dimethylpiperidin-2-yl]dodecan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H37NO2/c1-16(21)12-10-8-6-4-5-7-9-11-13-18-14-15-19(22)17(2)20(18)3/h17-19,22H,4-15H2,1-3H3/t17-,18-,19-/m0/s1
InChI Key AHRLVMHWPCQOGN-FHWLQOOXSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H37NO2
Molecular Weight 311.50 g/mol
Exact Mass 311.282429423 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.32
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 11

Synonyms

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75664-18-5
N-methylcassine
DTXSID70226578

2D Structure

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2D Structure of 2-Dodecanone, 12-(5-hydroxy-1,6-dimethyl-2-piperidinyl)-, (2S-(2alpha,5alpha,6alpha))-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9728 97.28%
Caco-2 + 0.5679 56.79%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.6581 65.81%
OATP2B1 inhibitior - 0.8519 85.19%
OATP1B1 inhibitior + 0.9527 95.27%
OATP1B3 inhibitior + 0.9423 94.23%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior + 0.8302 83.02%
P-glycoprotein inhibitior - 0.8465 84.65%
P-glycoprotein substrate - 0.6226 62.26%
CYP3A4 substrate + 0.5121 51.21%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.5089 50.89%
CYP3A4 inhibition - 0.8836 88.36%
CYP2C9 inhibition - 0.9503 95.03%
CYP2C19 inhibition - 0.9288 92.88%
CYP2D6 inhibition - 0.7001 70.01%
CYP1A2 inhibition - 0.7996 79.96%
CYP2C8 inhibition - 0.9735 97.35%
CYP inhibitory promiscuity - 0.9822 98.22%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7029 70.29%
Eye corrosion - 0.9637 96.37%
Eye irritation - 0.6439 64.39%
Skin irritation - 0.6123 61.23%
Skin corrosion - 0.6783 67.83%
Ames mutagenesis - 0.7937 79.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5712 57.12%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.5967 59.67%
skin sensitisation - 0.8416 84.16%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6392 63.92%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.8256 82.56%
Acute Oral Toxicity (c) III 0.7678 76.78%
Estrogen receptor binding - 0.5955 59.55%
Androgen receptor binding - 0.8833 88.33%
Thyroid receptor binding + 0.5906 59.06%
Glucocorticoid receptor binding - 0.5942 59.42%
Aromatase binding - 0.7280 72.80%
PPAR gamma - 0.5743 57.43%
Honey bee toxicity - 0.9544 95.44%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.5876 58.76%
Fish aquatic toxicity - 0.8864 88.64%

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 98.81% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.39% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 96.21% 83.82%
CHEMBL220 P22303 Acetylcholinesterase 91.97% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.84% 99.17%
CHEMBL325 Q13547 Histone deacetylase 1 87.74% 95.92%
CHEMBL217 P14416 Dopamine D2 receptor 87.15% 95.62%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.79% 85.14%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 85.45% 95.17%
CHEMBL5255 O00206 Toll-like receptor 4 85.42% 92.50%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.53% 95.89%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 84.41% 98.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.17% 97.25%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.76% 97.21%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.09% 97.09%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.95% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.64% 91.11%

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.
Neltuma nigra

Cross-Links

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PubChem 156624
LOTUS LTS0040929
wikiData Q83106048