Avenin

Details

Top
Internal ID 7710fe1e-77da-4c40-b6bf-b08a50ee188f
Taxonomy Organic acids and derivatives > Organic phosphoric acids and derivatives > Phosphate esters
IUPAC Name propan-2-yl N-dimethoxyphosphorylcarbamate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H14NO5P/c1-5(2)12-6(8)7-13(9,10-3)11-4/h5H,1-4H3,(H,7,8,9)
InChI Key XXRYFVCIMARHRS-UHFFFAOYSA-N
Popularity 388 references in papers

Physical and Chemical Properties

Top
Molecular Formula C6H14NO5P
Molecular Weight 211.15 g/mol
Exact Mass 211.06095954 g/mol
Topological Polar Surface Area (TPSA) 73.90 Ų
XlogP 0.20
Atomic LogP (AlogP) 1.52
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

Top
6309-98-4
Carbamic acid, (dimethoxyphosphinyl)-, 1-methylethyl ester
Isopropyl (dimethoxyphosphoryl)carbamate
Avenin (pesticide)
propan-2-yl N-dimethoxyphosphorylcarbamate
NSC 43003
BRN 1785625
Prolamins
AI3-31943
1-Methylethyl (dimethoxyphosphinyl)carbamate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Avenin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7044 70.44%
Caco-2 - 0.5427 54.27%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.7675 76.75%
OATP2B1 inhibitior - 0.8611 86.11%
OATP1B1 inhibitior + 0.9579 95.79%
OATP1B3 inhibitior + 0.9456 94.56%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9418 94.18%
P-glycoprotein inhibitior - 0.9255 92.55%
P-glycoprotein substrate - 0.9146 91.46%
CYP3A4 substrate - 0.5893 58.93%
CYP2C9 substrate - 0.8121 81.21%
CYP2D6 substrate - 0.8073 80.73%
CYP3A4 inhibition - 0.9466 94.66%
CYP2C9 inhibition - 0.8105 81.05%
CYP2C19 inhibition - 0.8403 84.03%
CYP2D6 inhibition - 0.9287 92.87%
CYP1A2 inhibition - 0.8270 82.70%
CYP2C8 inhibition - 0.9786 97.86%
CYP inhibitory promiscuity - 0.9504 95.04%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5963 59.63%
Carcinogenicity (trinary) Non-required 0.5862 58.62%
Eye corrosion - 0.8178 81.78%
Eye irritation - 0.5950 59.50%
Skin irritation - 0.6879 68.79%
Skin corrosion - 0.8715 87.15%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7814 78.14%
Micronuclear + 0.8400 84.00%
Hepatotoxicity - 0.5843 58.43%
skin sensitisation - 0.9053 90.53%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.7857 78.57%
Acute Oral Toxicity (c) I 0.3744 37.44%
Estrogen receptor binding - 0.8882 88.82%
Androgen receptor binding - 0.7224 72.24%
Thyroid receptor binding - 0.6881 68.81%
Glucocorticoid receptor binding - 0.9260 92.60%
Aromatase binding - 0.6940 69.40%
PPAR gamma - 0.9106 91.06%
Honey bee toxicity + 0.8735 87.35%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.7200 72.00%
Fish aquatic toxicity + 0.8128 81.28%

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 91.78% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.97% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.85% 94.45%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.09% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 81.89% 94.73%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.51% 94.33%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 81.44% 95.71%

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.
Alopecurus myosuroides

Cross-Links

Top
PubChem 95924
LOTUS LTS0106085
wikiData Q4055620