Methyl (1R,8R)-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1-carboxylate

Details

Top
Internal ID 28343326-2654-406d-9b44-557920e2ba42
Taxonomy Organoheterocyclic compounds > Pyrrolizidines
IUPAC Name methyl (1R,8R)-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H15NO2/c1-12-9(11)7-4-6-10-5-2-3-8(7)10/h7-8H,2-6H2,1H3/t7-,8-/m1/s1
InChI Key CFWZLIYRMYFCIH-HTQZYQBOSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C9H15NO2
Molecular Weight 169.22 g/mol
Exact Mass 169.110278721 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.64
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
22269-11-0
Methyl (1R,8R)-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1-carboxylate
AKOS040735297

2D Structure

Top
2D Structure of Methyl (1R,8R)-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1-carboxylate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9837 98.37%
Caco-2 + 0.8337 83.37%
Blood Brain Barrier + 0.8881 88.81%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.4954 49.54%
OATP2B1 inhibitior - 0.8360 83.60%
OATP1B1 inhibitior + 0.9634 96.34%
OATP1B3 inhibitior + 0.9517 95.17%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior + 0.5500 55.00%
BSEP inhibitior - 0.9199 91.99%
P-glycoprotein inhibitior - 0.9818 98.18%
P-glycoprotein substrate - 0.8353 83.53%
CYP3A4 substrate - 0.5679 56.79%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4591 45.91%
CYP3A4 inhibition - 0.9403 94.03%
CYP2C9 inhibition - 0.8829 88.29%
CYP2C19 inhibition - 0.8717 87.17%
CYP2D6 inhibition - 0.8287 82.87%
CYP1A2 inhibition - 0.6071 60.71%
CYP2C8 inhibition - 0.9763 97.63%
CYP inhibitory promiscuity - 0.9465 94.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5670 56.70%
Eye corrosion - 0.7998 79.98%
Eye irritation + 0.7043 70.43%
Skin irritation - 0.6664 66.64%
Skin corrosion - 0.7502 75.02%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5538 55.38%
Micronuclear - 0.7000 70.00%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation - 0.8616 86.16%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.6843 68.43%
Acute Oral Toxicity (c) III 0.4573 45.73%
Estrogen receptor binding - 0.9137 91.37%
Androgen receptor binding - 0.5994 59.94%
Thyroid receptor binding - 0.8981 89.81%
Glucocorticoid receptor binding - 0.8480 84.80%
Aromatase binding - 0.7469 74.69%
PPAR gamma - 0.9066 90.66%
Honey bee toxicity - 0.9601 96.01%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity - 0.8079 80.79%

Targets

Top

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 92.76% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.67% 98.95%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 85.94% 93.03%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.70% 94.45%
CHEMBL340 P08684 Cytochrome P450 3A4 84.46% 91.19%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.33% 94.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.31% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.35% 95.56%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 81.34% 95.50%

Plants that contains it

Top
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.
Osyris alba

Cross-Links

Top
PubChem 12345304
LOTUS LTS0016587
wikiData Q104376026