(8S,9aS)-6,8-dimethyl-1,2,3,4,7,8,9,9a-octahydroquinolizin-5-ium

Details

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Internal ID a15850e0-ee42-4362-9af9-523e50bbe675
Taxonomy Organoheterocyclic compounds > Quinolizines
IUPAC Name (8S,9aS)-6,8-dimethyl-1,2,3,4,7,8,9,9a-octahydroquinolizin-5-ium
SMILES (Canonical) CC1CC2CCCC[N+]2=C(C1)C
SMILES (Isomeric) C[C@H]1C[C@@H]2CCCC[N+]2=C(C1)C
InChI InChI=1S/C11H20N/c1-9-7-10(2)12-6-4-3-5-11(12)8-9/h9,11H,3-8H2,1-2H3/q+1/t9-,11+/m1/s1
InChI Key KLLZPXJSGZTYCM-KOLCDFICSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H20N+
Molecular Weight 166.28 g/mol
Exact Mass 166.159574642 g/mol
Topological Polar Surface Area (TPSA) 3.00 Ų
XlogP 1.50
Atomic LogP (AlogP) 2.44
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (8S,9aS)-6,8-dimethyl-1,2,3,4,7,8,9,9a-octahydroquinolizin-5-ium

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8374 83.74%
Caco-2 + 0.8786 87.86%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.6078 60.78%
OATP2B1 inhibitior - 0.8386 83.86%
OATP1B1 inhibitior + 0.9409 94.09%
OATP1B3 inhibitior + 0.9491 94.91%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior - 0.9495 94.95%
P-glycoprotein inhibitior - 0.9592 95.92%
P-glycoprotein substrate - 0.8695 86.95%
CYP3A4 substrate - 0.5797 57.97%
CYP2C9 substrate - 0.8052 80.52%
CYP2D6 substrate - 0.7493 74.93%
CYP3A4 inhibition - 0.9501 95.01%
CYP2C9 inhibition - 0.8483 84.83%
CYP2C19 inhibition - 0.7372 73.72%
CYP2D6 inhibition - 0.6660 66.60%
CYP1A2 inhibition - 0.8015 80.15%
CYP2C8 inhibition - 0.8749 87.49%
CYP inhibitory promiscuity - 0.9384 93.84%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.7017 70.17%
Eye corrosion - 0.6152 61.52%
Eye irritation + 0.8345 83.45%
Skin irritation + 0.5261 52.61%
Skin corrosion + 0.7850 78.50%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6612 66.12%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.6407 64.07%
skin sensitisation - 0.8363 83.63%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.6571 65.71%
Acute Oral Toxicity (c) III 0.6405 64.05%
Estrogen receptor binding - 0.8621 86.21%
Androgen receptor binding - 0.6154 61.54%
Thyroid receptor binding - 0.8770 87.70%
Glucocorticoid receptor binding - 0.9089 90.89%
Aromatase binding - 0.7604 76.04%
PPAR gamma - 0.8982 89.82%
Honey bee toxicity - 0.9356 93.56%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity + 0.8700 87.00%
Fish aquatic toxicity + 0.7988 79.88%

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
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 91.78% 86.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.46% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.82% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.55% 96.09%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 86.43% 90.71%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 84.69% 95.27%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.18% 94.80%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 81.75% 98.99%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.01% 95.89%
CHEMBL2039 P27338 Monoamine oxidase B 80.12% 92.51%

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.
Huperzia miyoshiana

Cross-Links

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PubChem 10241161
LOTUS LTS0006688
wikiData Q105142693