Propionate

Details

Top
Internal ID 827f4d41-a892-49f6-b2c0-c3abf2fd4eff
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acids
IUPAC Name propanoate
SMILES (Canonical) CCC(=O)[O-]
SMILES (Isomeric) CCC(=O)[O-]
InChI InChI=1S/C3H6O2/c1-2-3(4)5/h2H2,1H3,(H,4,5)/p-1
InChI Key XBDQKXXYIPTUBI-UHFFFAOYSA-M
Popularity 15,626 references in papers

Physical and Chemical Properties

Top
Molecular Formula C3H5O2-
Molecular Weight 73.07 g/mol
Exact Mass 73.028954398 g/mol
Topological Polar Surface Area (TPSA) 40.10 Ų
XlogP 0.90
Atomic LogP (AlogP) -0.85
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
propanoate
72-03-7
Propanoic acid, ion(1-)
Propanoic acid anion
Propionate ion
EtCO2 anion
AKW5EM890C
ANION STANDARD - PROPIONATE
metacetonate
propanate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Propionate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9850 98.50%
Caco-2 + 0.6440 64.40%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.5848 58.48%
OATP2B1 inhibitior - 0.8637 86.37%
OATP1B1 inhibitior + 0.9468 94.68%
OATP1B3 inhibitior + 0.9491 94.91%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9395 93.95%
P-glycoprotein inhibitior - 0.9889 98.89%
P-glycoprotein substrate - 0.9910 99.10%
CYP3A4 substrate - 0.7974 79.74%
CYP2C9 substrate + 0.6276 62.76%
CYP2D6 substrate - 0.8931 89.31%
CYP3A4 inhibition - 0.9774 97.74%
CYP2C9 inhibition - 0.9147 91.47%
CYP2C19 inhibition - 0.9546 95.46%
CYP2D6 inhibition - 0.9559 95.59%
CYP1A2 inhibition - 0.7849 78.49%
CYP2C8 inhibition - 0.9923 99.23%
CYP inhibitory promiscuity - 0.9608 96.08%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6354 63.54%
Carcinogenicity (trinary) Non-required 0.6164 61.64%
Eye corrosion + 1.0000 100.00%
Eye irritation + 0.9832 98.32%
Skin irritation + 0.9223 92.23%
Skin corrosion + 0.8949 89.49%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8258 82.58%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.5324 53.24%
skin sensitisation - 0.8830 88.30%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.4879 48.79%
Acute Oral Toxicity (c) III 0.8611 86.11%
Estrogen receptor binding - 0.9554 95.54%
Androgen receptor binding - 0.9389 93.89%
Thyroid receptor binding - 0.8968 89.68%
Glucocorticoid receptor binding - 0.9318 93.18%
Aromatase binding - 0.9111 91.11%
PPAR gamma - 0.8545 85.45%
Honey bee toxicity - 0.9813 98.13%
Biodegradation + 1.0000 100.00%
Crustacea aquatic toxicity - 0.8500 85.00%
Fish aquatic toxicity - 0.6428 64.28%

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 92.83% 96.09%
CHEMBL2581 P07339 Cathepsin D 84.46% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.67% 94.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.27% 96.95%

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.
Pogostemon cablin
Zingiber officinale

Cross-Links

Top
PubChem 104745
NPASS NPC238637