(5R,8R,8aS)-5-ethyl-8-methyl-1,2,3,5,6,7,8,8a-octahydroindolizine

Details

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Internal ID 1c500c80-eaf5-4bef-b1f8-0532397286e0
Taxonomy Organoheterocyclic compounds > Indolizidines
IUPAC Name (5R,8R,8aS)-5-ethyl-8-methyl-1,2,3,5,6,7,8,8a-octahydroindolizine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H21N/c1-3-10-7-6-9(2)11-5-4-8-12(10)11/h9-11H,3-8H2,1-2H3/t9-,10-,11+/m1/s1
InChI Key VHPIYWFQNXKJPH-MXWKQRLJSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H21N
Molecular Weight 167.29 g/mol
Exact Mass 167.167399674 g/mol
Topological Polar Surface Area (TPSA) 3.20 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.66
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (5R,8R,8aS)-5-ethyl-8-methyl-1,2,3,5,6,7,8,8a-octahydroindolizine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9914 99.14%
Caco-2 + 0.9112 91.12%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.6559 65.59%
OATP2B1 inhibitior - 0.8447 84.47%
OATP1B1 inhibitior + 0.9384 93.84%
OATP1B3 inhibitior + 0.9542 95.42%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.9256 92.56%
P-glycoprotein inhibitior - 0.9739 97.39%
P-glycoprotein substrate - 0.7695 76.95%
CYP3A4 substrate - 0.6485 64.85%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.6998 69.98%
CYP3A4 inhibition - 0.9813 98.13%
CYP2C9 inhibition - 0.8702 87.02%
CYP2C19 inhibition - 0.6916 69.16%
CYP2D6 inhibition - 0.7422 74.22%
CYP1A2 inhibition - 0.5096 50.96%
CYP2C8 inhibition - 0.9459 94.59%
CYP inhibitory promiscuity - 0.7947 79.47%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7182 71.82%
Eye corrosion - 0.6494 64.94%
Eye irritation + 0.9553 95.53%
Skin irritation - 0.5544 55.44%
Skin corrosion + 0.6740 67.40%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4563 45.63%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.7875 78.75%
skin sensitisation - 0.8382 83.82%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.7150 71.50%
Acute Oral Toxicity (c) III 0.5748 57.48%
Estrogen receptor binding - 0.9181 91.81%
Androgen receptor binding - 0.7597 75.97%
Thyroid receptor binding - 0.8356 83.56%
Glucocorticoid receptor binding - 0.8984 89.84%
Aromatase binding - 0.8305 83.05%
PPAR gamma - 0.9226 92.26%
Honey bee toxicity - 0.9853 98.53%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.8153 81.53%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.81% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.85% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.06% 98.95%
CHEMBL5203 P33316 dUTP pyrophosphatase 89.89% 99.18%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.49% 97.09%
CHEMBL1978 P11511 Cytochrome P450 19A1 86.23% 91.76%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.52% 95.89%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 81.21% 86.00%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 81.19% 98.46%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 163106292
LOTUS LTS0039514
wikiData Q105286551