Gephyrotoxin 207a

Details

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Internal ID 2634aeac-8846-4f95-9a32-d7a5987d49d7
Taxonomy Organoheterocyclic compounds > Indolizidines
IUPAC Name 8-methyl-5-pent-4-enyl-1,2,3,5,6,7,8,8a-octahydroindolizine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H25N/c1-3-4-5-7-13-10-9-12(2)14-8-6-11-15(13)14/h3,12-14H,1,4-11H2,2H3
InChI Key OHDBFRJCRJQLRN-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H25N
Molecular Weight 207.35 g/mol
Exact Mass 207.198699802 g/mol
Topological Polar Surface Area (TPSA) 3.20 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.61
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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OHDBFRJCRJQLRN-UHFFFAOYSA-N
8-Methyl-5-(4-pentenyl)octahydroindolizine #

2D Structure

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2D Structure of Gephyrotoxin 207a

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9890 98.90%
Caco-2 + 0.9134 91.34%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.4545 45.45%
OATP2B1 inhibitior - 0.8522 85.22%
OATP1B1 inhibitior + 0.9163 91.63%
OATP1B3 inhibitior + 0.9492 94.92%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior + 0.5500 55.00%
BSEP inhibitior - 0.8270 82.70%
P-glycoprotein inhibitior - 0.9615 96.15%
P-glycoprotein substrate - 0.6873 68.73%
CYP3A4 substrate - 0.5144 51.44%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.6494 64.94%
CYP3A4 inhibition - 0.9873 98.73%
CYP2C9 inhibition - 0.8644 86.44%
CYP2C19 inhibition - 0.6222 62.22%
CYP2D6 inhibition - 0.7586 75.86%
CYP1A2 inhibition - 0.5474 54.74%
CYP2C8 inhibition - 0.8581 85.81%
CYP inhibitory promiscuity - 0.7884 78.84%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6303 63.03%
Eye corrosion - 0.7392 73.92%
Eye irritation + 0.6453 64.53%
Skin irritation + 0.5182 51.82%
Skin corrosion + 0.6628 66.28%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4662 46.62%
Micronuclear - 0.8900 89.00%
Hepatotoxicity + 0.7065 70.65%
skin sensitisation - 0.7784 77.84%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.5911 59.11%
Acute Oral Toxicity (c) III 0.6806 68.06%
Estrogen receptor binding - 0.8137 81.37%
Androgen receptor binding - 0.7985 79.85%
Thyroid receptor binding - 0.6833 68.33%
Glucocorticoid receptor binding - 0.5660 56.60%
Aromatase binding - 0.6957 69.57%
PPAR gamma - 0.7256 72.56%
Honey bee toxicity - 0.9483 94.83%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9318 93.18%

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 93.90% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.76% 98.95%
CHEMBL5203 P33316 dUTP pyrophosphatase 91.96% 99.18%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.18% 97.25%
CHEMBL1978 P11511 Cytochrome P450 19A1 89.15% 91.76%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 87.38% 86.00%
CHEMBL1902 P62942 FK506-binding protein 1A 87.04% 97.05%
CHEMBL264 Q9Y5N1 Histamine H3 receptor 85.50% 91.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.74% 95.89%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 84.06% 95.50%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.49% 91.11%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 83.47% 98.33%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 83.34% 82.38%
CHEMBL1871 P10275 Androgen Receptor 83.33% 96.43%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 83.10% 93.40%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.94% 97.09%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.23% 93.00%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 81.86% 90.24%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.05% 86.33%

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 586750
LOTUS LTS0249610
wikiData Q105192013