4-Oxohomoanatoxin-A

Details

Top
Internal ID f4a03c1c-6451-4304-8432-4684559bd3ba
Taxonomy Alkaloids and derivatives > Anatoxins
IUPAC Name (1S,6R)-5-propanoyl-9-azabicyclo[4.2.1]non-4-en-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H15NO2/c1-2-11(14)9-6-8(13)5-7-3-4-10(9)12-7/h6-7,10,12H,2-5H2,1H3/t7-,10+/m0/s1
InChI Key OQSWFCINTWWZIB-OIBJUYFYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

Top
Molecular Formula C11H15NO2
Molecular Weight 193.24 g/mol
Exact Mass 193.110278721 g/mol
Topological Polar Surface Area (TPSA) 46.20 Ų
XlogP 0.10
Atomic LogP (AlogP) 0.99
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

Top
823234-71-5
DTXSID80838363

2D Structure

Top
2D Structure of 4-Oxohomoanatoxin-A

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8561 85.61%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.5206 52.06%
OATP2B1 inhibitior - 0.8539 85.39%
OATP1B1 inhibitior + 0.9155 91.55%
OATP1B3 inhibitior + 0.9526 95.26%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.8704 87.04%
P-glycoprotein inhibitior - 0.9592 95.92%
P-glycoprotein substrate - 0.6926 69.26%
CYP3A4 substrate - 0.5661 56.61%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7774 77.74%
CYP3A4 inhibition - 0.8850 88.50%
CYP2C9 inhibition - 0.7446 74.46%
CYP2C19 inhibition - 0.7412 74.12%
CYP2D6 inhibition - 0.8408 84.08%
CYP1A2 inhibition - 0.6192 61.92%
CYP2C8 inhibition - 0.9390 93.90%
CYP inhibitory promiscuity - 0.5998 59.98%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5947 59.47%
Eye corrosion - 0.9583 95.83%
Eye irritation + 0.7388 73.88%
Skin irritation - 0.7615 76.15%
Skin corrosion - 0.9120 91.20%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6416 64.16%
Micronuclear - 0.6200 62.00%
Hepatotoxicity + 0.5087 50.87%
skin sensitisation - 0.8031 80.31%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.5997 59.97%
Acute Oral Toxicity (c) III 0.6627 66.27%
Estrogen receptor binding - 0.7747 77.47%
Androgen receptor binding - 0.6248 62.48%
Thyroid receptor binding - 0.6126 61.26%
Glucocorticoid receptor binding - 0.8260 82.60%
Aromatase binding - 0.8595 85.95%
PPAR gamma - 0.8182 81.82%
Honey bee toxicity - 0.9383 93.83%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity - 0.6365 63.65%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.04% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.85% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.55% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.92% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.33% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.16% 96.95%
CHEMBL255 P29275 Adenosine A2b receptor 84.70% 98.59%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.30% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.49% 94.45%
CHEMBL1907589 P17787 Neuronal acetylcholine receptor; alpha4/beta2 82.24% 94.55%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.51% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 80.38% 90.17%

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.
There are no matching plants.

Cross-Links

Top
PubChem 71419096
LOTUS LTS0004158
wikiData Q82826819