(5S,6R,8R,8aS)-6,8-diethyl-5-pentyl-1,2,3,5,6,7,8,8a-octahydroindolizine

Details

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Internal ID d7832a4a-3fc1-48fd-814b-35e1b58966b0
Taxonomy Organoheterocyclic compounds > Indolizidines
IUPAC Name (5S,6R,8R,8aS)-6,8-diethyl-5-pentyl-1,2,3,5,6,7,8,8a-octahydroindolizine
SMILES (Canonical) CCCCCC1C(CC(C2N1CCC2)CC)CC
SMILES (Isomeric) CCCCC[C@H]1[C@@H](C[C@H]([C@H]2N1CCC2)CC)CC
InChI InChI=1S/C17H33N/c1-4-7-8-10-16-14(5-2)13-15(6-3)17-11-9-12-18(16)17/h14-17H,4-13H2,1-3H3/t14-,15-,16+,17+/m1/s1
InChI Key CWJWDXLGJFRHSV-NCOADZHNSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H33N
Molecular Weight 251.50 g/mol
Exact Mass 251.261300057 g/mol
Topological Polar Surface Area (TPSA) 3.20 Ų
XlogP 5.70
Atomic LogP (AlogP) 4.86
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (5S,6R,8R,8aS)-6,8-diethyl-5-pentyl-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 + 0.9894 98.94%
Caco-2 + 0.8846 88.46%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Lysosomes 0.5358 53.58%
OATP2B1 inhibitior - 0.8485 84.85%
OATP1B1 inhibitior + 0.9183 91.83%
OATP1B3 inhibitior + 0.9525 95.25%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior - 0.7685 76.85%
P-glycoprotein inhibitior - 0.9029 90.29%
P-glycoprotein substrate - 0.5052 50.52%
CYP3A4 substrate - 0.5533 55.33%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.6998 69.98%
CYP3A4 inhibition - 0.9730 97.30%
CYP2C9 inhibition - 0.8366 83.66%
CYP2C19 inhibition - 0.6205 62.05%
CYP2D6 inhibition - 0.7514 75.14%
CYP1A2 inhibition + 0.5693 56.93%
CYP2C8 inhibition - 0.8950 89.50%
CYP inhibitory promiscuity - 0.7413 74.13%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6899 68.99%
Eye corrosion - 0.8017 80.17%
Eye irritation + 0.6477 64.77%
Skin irritation - 0.5710 57.10%
Skin corrosion + 0.6058 60.58%
Ames mutagenesis - 0.8337 83.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5665 56.65%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.6808 68.08%
skin sensitisation - 0.8509 85.09%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity + 0.6202 62.02%
Acute Oral Toxicity (c) III 0.6028 60.28%
Estrogen receptor binding - 0.5598 55.98%
Androgen receptor binding - 0.4935 49.35%
Thyroid receptor binding - 0.5101 51.01%
Glucocorticoid receptor binding - 0.7349 73.49%
Aromatase binding - 0.7837 78.37%
PPAR gamma - 0.8316 83.16%
Honey bee toxicity - 0.9814 98.14%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6682 66.82%
Fish aquatic toxicity + 0.8763 87.63%

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 98.62% 97.25%
CHEMBL2581 P07339 Cathepsin D 96.53% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.31% 96.09%
CHEMBL1978 P11511 Cytochrome P450 19A1 94.19% 91.76%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.73% 97.09%
CHEMBL5203 P33316 dUTP pyrophosphatase 89.91% 99.18%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 89.57% 95.50%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 89.09% 91.81%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 88.75% 95.58%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 86.39% 100.00%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 85.59% 90.24%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 85.51% 92.86%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 84.47% 82.38%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 84.20% 98.33%
CHEMBL2996 Q05655 Protein kinase C delta 84.01% 97.79%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 83.63% 90.24%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 83.50% 90.71%
CHEMBL230 P35354 Cyclooxygenase-2 83.40% 89.63%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.39% 95.89%
CHEMBL228 P31645 Serotonin transporter 83.34% 95.51%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.96% 93.56%
CHEMBL240 Q12809 HERG 82.38% 89.76%
CHEMBL1871 P10275 Androgen Receptor 81.26% 96.43%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 80.79% 97.50%
CHEMBL226 P30542 Adenosine A1 receptor 80.38% 95.93%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.22% 92.08%

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.
Callitris columellaris

Cross-Links

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PubChem 162964490
LOTUS LTS0097455
wikiData Q105252353