(Hexahydro-2,4-methano-4H-furo[3,2-B]pyrrol-3-YL)methylcarbamic acid [6-acetylamino-4-chloro-1-azabicyclo[3.3.0]octan-7-YL] ester

Details

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Internal ID 09bfb740-53b2-4267-b5d1-79ef1bb016d9
Taxonomy Organoheterocyclic compounds > Pyrrolizidines
IUPAC Name (1-acetamido-7-chloro-2,3,5,6,7,8-hexahydro-1H-pyrrolizin-2-yl) N-(2-oxa-6-azatricyclo[4.2.1.03,7]nonan-8-ylmethyl)carbamate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H27ClN4O4/c1-9(24)21-15-14(8-23-4-2-11(19)17(15)23)27-18(25)20-6-10-13-7-22-5-3-12(26-13)16(10)22/h10-17H,2-8H2,1H3,(H,20,25)(H,21,24)
InChI Key MEQYZLVMLXTKEV-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H27ClN4O4
Molecular Weight 398.90 g/mol
Exact Mass 398.1720830 g/mol
Topological Polar Surface Area (TPSA) 83.10 Ų
XlogP 0.10
Atomic LogP (AlogP) -0.25
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (Hexahydro-2,4-methano-4H-furo[3,2-B]pyrrol-3-YL)methylcarbamic acid [6-acetylamino-4-chloro-1-azabicyclo[3.3.0]octan-7-YL] ester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9247 92.47%
Caco-2 - 0.5992 59.92%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Lysosomes 0.6124 61.24%
OATP2B1 inhibitior - 0.8579 85.79%
OATP1B1 inhibitior + 0.8605 86.05%
OATP1B3 inhibitior + 0.9376 93.76%
MATE1 inhibitior - 0.7217 72.17%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7094 70.94%
P-glycoprotein inhibitior - 0.6202 62.02%
P-glycoprotein substrate + 0.6208 62.08%
CYP3A4 substrate + 0.6763 67.63%
CYP2C9 substrate - 0.8177 81.77%
CYP2D6 substrate - 0.7235 72.35%
CYP3A4 inhibition - 0.7729 77.29%
CYP2C9 inhibition - 0.7173 71.73%
CYP2C19 inhibition + 0.5682 56.82%
CYP2D6 inhibition - 0.8453 84.53%
CYP1A2 inhibition - 0.7116 71.16%
CYP2C8 inhibition - 0.7009 70.09%
CYP inhibitory promiscuity + 0.5552 55.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.5605 56.05%
Eye corrosion - 0.9847 98.47%
Eye irritation - 0.9748 97.48%
Skin irritation - 0.7674 76.74%
Skin corrosion - 0.9325 93.25%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.8900 89.00%
Hepatotoxicity + 0.7426 74.26%
skin sensitisation - 0.8659 86.59%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity + 0.7521 75.21%
Acute Oral Toxicity (c) III 0.5781 57.81%
Estrogen receptor binding - 0.6953 69.53%
Androgen receptor binding - 0.5250 52.50%
Thyroid receptor binding + 0.5296 52.96%
Glucocorticoid receptor binding - 0.5315 53.15%
Aromatase binding + 0.5208 52.08%
PPAR gamma + 0.5805 58.05%
Honey bee toxicity - 0.5482 54.82%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.7661 76.61%

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 95.99% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.25% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 94.16% 96.95%
CHEMBL2581 P07339 Cathepsin D 91.79% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.22% 97.25%
CHEMBL4588 P22894 Matrix metalloproteinase 8 90.51% 94.66%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 88.67% 97.21%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 88.60% 92.29%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 87.51% 94.33%
CHEMBL340 P08684 Cytochrome P450 3A4 86.99% 91.19%
CHEMBL3437 Q16853 Amine oxidase, copper containing 86.12% 94.00%
CHEMBL4208 P20618 Proteasome component C5 84.42% 90.00%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 83.38% 80.33%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 83.08% 98.33%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 82.87% 95.50%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.67% 94.45%
CHEMBL5028 O14672 ADAM10 81.73% 97.50%
CHEMBL5255 O00206 Toll-like receptor 4 81.64% 92.50%
CHEMBL2413 P32246 C-C chemokine receptor type 1 81.49% 89.50%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 81.41% 97.50%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.28% 97.28%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 81.02% 95.58%
CHEMBL3691 Q13822 Autotaxin 80.58% 96.39%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.41% 95.89%

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.
Lolium temulentum

Cross-Links

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PubChem 101316803
LOTUS LTS0187792
wikiData Q105162376