1-(1-Methylpyrrolidin-1-ium-2-yl)propan-2-one

Details

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Internal ID 7eb14335-dcba-41ee-a870-2c28685d9d2a
Taxonomy Alkaloids and derivatives
IUPAC Name 1-(1-methylpyrrolidin-1-ium-2-yl)propan-2-one
SMILES (Canonical) CC(=O)CC1CCC[NH+]1C
SMILES (Isomeric) CC(=O)CC1CCC[NH+]1C
InChI InChI=1S/C8H15NO/c1-7(10)6-8-4-3-5-9(8)2/h8H,3-6H2,1-2H3/p+1
InChI Key ADKXZIOQKHHDNQ-UHFFFAOYSA-O
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H16NO+
Molecular Weight 142.22 g/mol
Exact Mass 142.123189134 g/mol
Topological Polar Surface Area (TPSA) 21.50 Ų
XlogP 0.50
Atomic LogP (AlogP) -0.36
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(1-Methylpyrrolidin-1-ium-2-yl)propan-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8841 88.41%
Caco-2 + 0.9177 91.77%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.8385 83.85%
OATP2B1 inhibitior - 0.8358 83.58%
OATP1B1 inhibitior + 0.9527 95.27%
OATP1B3 inhibitior + 0.9396 93.96%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior - 0.9553 95.53%
P-glycoprotein inhibitior - 0.9792 97.92%
P-glycoprotein substrate - 0.9121 91.21%
CYP3A4 substrate - 0.5853 58.53%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3665 36.65%
CYP3A4 inhibition - 0.9814 98.14%
CYP2C9 inhibition - 0.9434 94.34%
CYP2C19 inhibition - 0.9109 91.09%
CYP2D6 inhibition - 0.8784 87.84%
CYP1A2 inhibition - 0.8715 87.15%
CYP2C8 inhibition - 0.9662 96.62%
CYP inhibitory promiscuity - 0.9868 98.68%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.7041 70.41%
Eye corrosion - 0.8800 88.00%
Eye irritation + 0.9050 90.50%
Skin irritation - 0.6576 65.76%
Skin corrosion - 0.5203 52.03%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6180 61.80%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.6458 64.58%
skin sensitisation - 0.8897 88.97%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.5763 57.63%
Acute Oral Toxicity (c) III 0.6474 64.74%
Estrogen receptor binding - 0.9358 93.58%
Androgen receptor binding - 0.8921 89.21%
Thyroid receptor binding - 0.9089 90.89%
Glucocorticoid receptor binding - 0.9083 90.83%
Aromatase binding - 0.8019 80.19%
PPAR gamma - 0.9360 93.60%
Honey bee toxicity - 0.9396 93.96%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity - 0.8217 82.17%

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 95.63% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 91.84% 83.82%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.82% 95.50%
CHEMBL2581 P07339 Cathepsin D 82.14% 98.95%
CHEMBL340 P08684 Cytochrome P450 3A4 81.84% 91.19%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.49% 94.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.12% 97.09%

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.
Dendrobium chrysanthum
Rosmarinus officinalis

Cross-Links

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PubChem 25200410
NPASS NPC190245