(2R,3R,6S)-2-methyl-6-(9-phenylnonyl)piperidin-3-ol

Details

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Internal ID 271171d4-a9fd-4415-8f2d-fd5d7d57dd57
Taxonomy Alkaloids and derivatives
IUPAC Name (2R,3R,6S)-2-methyl-6-(9-phenylnonyl)piperidin-3-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H35NO/c1-18-21(23)17-16-20(22-18)15-11-6-4-2-3-5-8-12-19-13-9-7-10-14-19/h7,9-10,13-14,18,20-23H,2-6,8,11-12,15-17H2,1H3/t18-,20+,21-/m1/s1
InChI Key XFSGJROMOFEUFI-HLAWJBBLSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C21H35NO
Molecular Weight 317.50 g/mol
Exact Mass 317.271864740 g/mol
Topological Polar Surface Area (TPSA) 32.30 Ų
XlogP 6.10
Atomic LogP (AlogP) 4.85
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,3R,6S)-2-methyl-6-(9-phenylnonyl)piperidin-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9847 98.47%
Caco-2 + 0.6008 60.08%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6216 62.16%
OATP2B1 inhibitior - 0.8566 85.66%
OATP1B1 inhibitior + 0.9125 91.25%
OATP1B3 inhibitior + 0.9531 95.31%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.5434 54.34%
P-glycoprotein inhibitior - 0.7980 79.80%
P-glycoprotein substrate + 0.6239 62.39%
CYP3A4 substrate + 0.5000 50.00%
CYP2C9 substrate - 0.7945 79.45%
CYP2D6 substrate + 0.6811 68.11%
CYP3A4 inhibition - 0.8187 81.87%
CYP2C9 inhibition - 0.9401 94.01%
CYP2C19 inhibition - 0.8597 85.97%
CYP2D6 inhibition - 0.5763 57.63%
CYP1A2 inhibition - 0.7826 78.26%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity - 0.8890 88.90%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6996 69.96%
Eye corrosion - 0.9315 93.15%
Eye irritation - 0.9525 95.25%
Skin irritation - 0.5640 56.40%
Skin corrosion - 0.5795 57.95%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7874 78.74%
Micronuclear - 0.5100 51.00%
Hepatotoxicity - 0.5374 53.74%
skin sensitisation - 0.7832 78.32%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.8302 83.02%
Acute Oral Toxicity (c) III 0.7220 72.20%
Estrogen receptor binding + 0.7376 73.76%
Androgen receptor binding - 0.6980 69.80%
Thyroid receptor binding + 0.7001 70.01%
Glucocorticoid receptor binding - 0.6943 69.43%
Aromatase binding - 0.5133 51.33%
PPAR gamma + 0.7122 71.22%
Honey bee toxicity - 0.9663 96.63%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.5850 58.50%
Fish aquatic toxicity - 0.6527 65.27%

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 98.20% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.79% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.39% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.95% 97.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 88.12% 94.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.36% 95.56%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 85.51% 91.71%
CHEMBL226 P30542 Adenosine A1 receptor 85.38% 95.93%
CHEMBL3202 P48147 Prolyl endopeptidase 85.33% 90.65%
CHEMBL5805 Q9NR97 Toll-like receptor 8 85.30% 96.25%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 85.25% 97.64%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.20% 86.33%
CHEMBL2959 Q08881 Tyrosine-protein kinase ITK/TSK 83.20% 95.00%

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.
Arisarum vulgare

Cross-Links

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PubChem 10925178
LOTUS LTS0172422
wikiData Q105327250