Methylisopelletierine

Details

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Internal ID b8912a7f-b7b1-40bd-a0f3-fcb2b189ce21
Taxonomy Organoheterocyclic compounds > Piperidines
IUPAC Name 1-(1-methylpiperidin-2-yl)propan-2-one
SMILES (Canonical) CC(=O)CC1CCCCN1C
SMILES (Isomeric) CC(=O)CC1CCCCN1C
InChI InChI=1S/C9H17NO/c1-8(11)7-9-5-3-4-6-10(9)2/h9H,3-7H2,1-2H3
InChI Key TYHJMEIBGDDCPA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H17NO
Molecular Weight 155.24 g/mol
Exact Mass 155.131014166 g/mol
Topological Polar Surface Area (TPSA) 20.30 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.45
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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18747-42-7
1-(1-methylpiperidin-2-yl)propan-2-one
N-Methylisopelletierine
1-(1-Methyl-2-piperidinyl)acetone
Methylisopunicine
(+/-)-N-Methylpelletierine
(+/-)-1-Methylpelletierine
N-Methylpelletierine, (+/-)-
UNII-7A42OMR1WL
7A42OMR1WL
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Methylisopelletierine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9463 94.63%
Caco-2 + 0.9216 92.16%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6428 64.28%
OATP2B1 inhibitior - 0.8357 83.57%
OATP1B1 inhibitior + 0.9593 95.93%
OATP1B3 inhibitior + 0.9469 94.69%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior + 0.6500 65.00%
BSEP inhibitior - 0.9332 93.32%
P-glycoprotein inhibitior - 0.9804 98.04%
P-glycoprotein substrate - 0.7883 78.83%
CYP3A4 substrate - 0.5996 59.96%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.5193 51.93%
CYP3A4 inhibition - 0.9891 98.91%
CYP2C9 inhibition - 0.9341 93.41%
CYP2C19 inhibition - 0.8344 83.44%
CYP2D6 inhibition - 0.9207 92.07%
CYP1A2 inhibition - 0.6191 61.91%
CYP2C8 inhibition - 0.9957 99.57%
CYP inhibitory promiscuity - 0.9849 98.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.7044 70.44%
Eye corrosion - 0.8743 87.43%
Eye irritation + 0.8588 85.88%
Skin irritation + 0.5465 54.65%
Skin corrosion + 0.6677 66.77%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6199 61.99%
Micronuclear - 0.8600 86.00%
Hepatotoxicity + 0.5161 51.61%
skin sensitisation - 0.8405 84.05%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.8027 80.27%
Acute Oral Toxicity (c) III 0.7993 79.93%
Estrogen receptor binding - 0.9391 93.91%
Androgen receptor binding - 0.8787 87.87%
Thyroid receptor binding - 0.8607 86.07%
Glucocorticoid receptor binding - 0.8732 87.32%
Aromatase binding - 0.7775 77.75%
PPAR gamma - 0.9235 92.35%
Honey bee toxicity - 0.9669 96.69%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity - 0.8591 85.91%

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 98.46% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.56% 97.25%
CHEMBL2581 P07339 Cathepsin D 91.75% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 88.78% 83.82%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 88.72% 93.04%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 84.67% 95.50%
CHEMBL4072 P07858 Cathepsin B 83.22% 93.67%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 81.87% 98.33%
CHEMBL5203 P33316 dUTP pyrophosphatase 81.60% 99.18%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.64% 95.56%

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.
Phedimus aizoon
Picea breweriana
Punica granatum

Cross-Links

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PubChem 86786
NPASS NPC224116
LOTUS LTS0082336
wikiData Q27107473