n-(Hexahydro-1h-1,6-epoxypyrrolizin-7-yl)-n-methylformamide

Details

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Internal ID 18f95812-169a-4802-aff9-b22aedffc5b5
Taxonomy Alkaloids and derivatives > Loline alkaloids and derivatives
IUPAC Name N-methyl-N-(2-oxa-6-azatricyclo[4.2.1.03,7]nonan-8-yl)formamide
SMILES (Canonical) CN(C=O)C1C2CN3C1C(O2)CC3
SMILES (Isomeric) CN(C=O)C1C2CN3C1C(O2)CC3
InChI InChI=1S/C9H14N2O2/c1-10(5-12)8-7-4-11-3-2-6(13-7)9(8)11/h5-9H,2-4H2,1H3
InChI Key YHLKXYXFUCTURZ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C9H14N2O2
Molecular Weight 182.22 g/mol
Exact Mass 182.105527694 g/mol
Topological Polar Surface Area (TPSA) 32.80 Ų
XlogP -0.40
Atomic LogP (AlogP) -0.70
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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DTXSID60959808

2D Structure

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2D Structure of n-(Hexahydro-1h-1,6-epoxypyrrolizin-7-yl)-n-methylformamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9666 96.66%
Caco-2 + 0.8025 80.25%
Blood Brain Barrier + 0.9129 91.29%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.4035 40.35%
OATP2B1 inhibitior - 0.8554 85.54%
OATP1B1 inhibitior + 0.9419 94.19%
OATP1B3 inhibitior + 0.9476 94.76%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.9836 98.36%
P-glycoprotein inhibitior - 0.9705 97.05%
P-glycoprotein substrate - 0.7672 76.72%
CYP3A4 substrate + 0.5656 56.56%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate + 0.4478 44.78%
CYP3A4 inhibition - 0.9634 96.34%
CYP2C9 inhibition - 0.9147 91.47%
CYP2C19 inhibition - 0.8196 81.96%
CYP2D6 inhibition - 0.9343 93.43%
CYP1A2 inhibition - 0.8356 83.56%
CYP2C8 inhibition - 0.9764 97.64%
CYP inhibitory promiscuity - 0.9264 92.64%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6700 67.00%
Eye corrosion - 0.9601 96.01%
Eye irritation - 0.8364 83.64%
Skin irritation - 0.7222 72.22%
Skin corrosion - 0.8275 82.75%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4219 42.19%
Micronuclear + 0.6100 61.00%
Hepatotoxicity + 0.8052 80.52%
skin sensitisation - 0.8667 86.67%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity + 0.7724 77.24%
Acute Oral Toxicity (c) III 0.7046 70.46%
Estrogen receptor binding - 0.8729 87.29%
Androgen receptor binding - 0.7382 73.82%
Thyroid receptor binding - 0.6839 68.39%
Glucocorticoid receptor binding - 0.7770 77.70%
Aromatase binding - 0.8481 84.81%
PPAR gamma - 0.8291 82.91%
Honey bee toxicity - 0.7455 74.55%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity - 0.9564 95.64%

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 94.16% 96.09%
CHEMBL274 P51681 C-C chemokine receptor type 5 89.24% 98.77%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 87.82% 97.47%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.59% 93.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 81.59% 90.08%
CHEMBL4588 P22894 Matrix metalloproteinase 8 81.32% 94.66%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 81.20% 94.78%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.53% 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.
Argyreia mollis
Festuca rubra
Lolium temulentum

Cross-Links

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PubChem 107859
LOTUS LTS0233743
wikiData Q82940713