Calibration Solution Certified Reference Material for Homoanatoxin-a

Details

Top
Internal ID d5521afb-7763-4ae3-bc2c-ad7113638680
Taxonomy Alkaloids and derivatives > Anatoxins
IUPAC Name 1-(9-azabicyclo[4.2.1]non-2-en-2-yl)propan-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H17NO/c1-2-11(13)9-5-3-4-8-6-7-10(9)12-8/h5,8,10,12H,2-4,6-7H2,1H3
InChI Key VVMQRZZXKNDPOT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C11H17NO
Molecular Weight 179.26 g/mol
Exact Mass 179.131014166 g/mol
Topological Polar Surface Area (TPSA) 29.10 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.81
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Calibration Solution Certified Reference Material for Homoanatoxin-a

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8508 85.08%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.4431 44.31%
OATP2B1 inhibitior - 0.8450 84.50%
OATP1B1 inhibitior + 0.9439 94.39%
OATP1B3 inhibitior + 0.9499 94.99%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior + 0.5750 57.50%
BSEP inhibitior - 0.8513 85.13%
P-glycoprotein inhibitior - 0.9731 97.31%
P-glycoprotein substrate - 0.8313 83.13%
CYP3A4 substrate - 0.6062 60.62%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7774 77.74%
CYP3A4 inhibition - 0.9183 91.83%
CYP2C9 inhibition - 0.7447 74.47%
CYP2C19 inhibition - 0.6821 68.21%
CYP2D6 inhibition - 0.8343 83.43%
CYP1A2 inhibition + 0.5812 58.12%
CYP2C8 inhibition - 0.9083 90.83%
CYP inhibitory promiscuity + 0.5700 57.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.6404 64.04%
Eye corrosion - 0.9370 93.70%
Eye irritation + 0.7869 78.69%
Skin irritation - 0.6909 69.09%
Skin corrosion - 0.8624 86.24%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4198 41.98%
Micronuclear - 0.7200 72.00%
Hepatotoxicity - 0.5822 58.22%
skin sensitisation - 0.7628 76.28%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6780 67.80%
Acute Oral Toxicity (c) III 0.6647 66.47%
Estrogen receptor binding - 0.9183 91.83%
Androgen receptor binding - 0.7944 79.44%
Thyroid receptor binding - 0.7570 75.70%
Glucocorticoid receptor binding - 0.8936 89.36%
Aromatase binding - 0.8485 84.85%
PPAR gamma - 0.8880 88.80%
Honey bee toxicity - 0.9530 95.30%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity - 0.6508 65.08%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.51% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.62% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.32% 97.09%
CHEMBL4040 P28482 MAP kinase ERK2 90.84% 83.82%
CHEMBL1907589 P17787 Neuronal acetylcholine receptor; alpha4/beta2 86.16% 94.55%
CHEMBL2581 P07339 Cathepsin D 85.35% 98.95%
CHEMBL4208 P20618 Proteasome component C5 85.15% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.63% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.40% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.26% 91.11%

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 20056049
LOTUS LTS0147991
wikiData Q104199819