1-Methylhexahydro-1H-pyrrolizine

Details

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Internal ID 7eb78356-72f4-41b3-83f5-b481ad6e5911
Taxonomy Organoheterocyclic compounds > Pyrrolizidines
IUPAC Name 1-methyl-2,3,5,6,7,8-hexahydro-1H-pyrrolizine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H15N/c1-7-4-6-9-5-2-3-8(7)9/h7-8H,2-6H2,1H3
InChI Key BFHBAQJJQJPDGF-UHFFFAOYSA-N
Popularity 17 references in papers

Physical and Chemical Properties

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Molecular Formula C8H15N
Molecular Weight 125.21 g/mol
Exact Mass 125.120449483 g/mol
Topological Polar Surface Area (TPSA) 3.20 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.49
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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100860-09-1
1-methyl-2,3,5,6,7,8-hexahydro-1H-pyrrolizine
1H-Pyrrolizine,2,3,5,7a-tetrahydro-7-methyl-(6CI)
1-methylpyrrolizidine
NoName_3457
SCHEMBL2618397
CHEMBL2448854
DTXSID90902882

2D Structure

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2D Structure of 1-Methylhexahydro-1H-pyrrolizine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9870 98.70%
Caco-2 + 0.8920 89.20%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.8626 86.26%
OATP2B1 inhibitior - 0.8456 84.56%
OATP1B1 inhibitior + 0.9595 95.95%
OATP1B3 inhibitior + 0.9541 95.41%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior + 0.5500 55.00%
BSEP inhibitior - 0.9393 93.93%
P-glycoprotein inhibitior - 0.9881 98.81%
P-glycoprotein substrate - 0.9059 90.59%
CYP3A4 substrate - 0.6711 67.11%
CYP2C9 substrate - 0.8388 83.88%
CYP2D6 substrate + 0.6443 64.43%
CYP3A4 inhibition - 0.9923 99.23%
CYP2C9 inhibition - 0.9184 91.84%
CYP2C19 inhibition - 0.7932 79.32%
CYP2D6 inhibition - 0.8592 85.92%
CYP1A2 inhibition - 0.8298 82.98%
CYP2C8 inhibition - 0.9909 99.09%
CYP inhibitory promiscuity - 0.9406 94.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5253 52.53%
Eye corrosion + 0.7939 79.39%
Eye irritation + 0.9558 95.58%
Skin irritation + 0.6104 61.04%
Skin corrosion + 0.8396 83.96%
Ames mutagenesis - 0.8054 80.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6497 64.97%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.9250 92.50%
skin sensitisation - 0.8848 88.48%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity + 0.5485 54.85%
Acute Oral Toxicity (c) III 0.5380 53.80%
Estrogen receptor binding - 0.9582 95.82%
Androgen receptor binding - 0.8159 81.59%
Thyroid receptor binding - 0.9154 91.54%
Glucocorticoid receptor binding - 0.9135 91.35%
Aromatase binding - 0.8997 89.97%
PPAR gamma - 0.9364 93.64%
Honey bee toxicity - 0.9753 97.53%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.7300 73.00%
Fish aquatic toxicity - 0.4141 41.41%

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
CHEMBL2581 P07339 Cathepsin D 89.01% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.86% 97.25%
CHEMBL5203 P33316 dUTP pyrophosphatase 87.58% 99.18%
CHEMBL264 Q9Y5N1 Histamine H3 receptor 85.61% 91.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.25% 95.89%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.91% 86.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.89% 97.09%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 80.56% 98.46%

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.
Crotalaria damarensis

Cross-Links

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PubChem 15559671
LOTUS LTS0022319
wikiData Q104250406