Status : experimental

Chemical Classification

This compound belongs to the class of organic compounds known as beta amino acids and derivatives. These are amino acids having a (-NH2) group attached to the beta carbon atom.

Beta amino acids and derivatives

Organic compounds

Organic acids and derivatives

Carboxylic acids and derivatives

Amino acids, peptides, and analogues

Calculated Property

kind Value Source
logP 0.16 ALOGPS
logS -3.1 ALOGPS
Water Solubility 2.20e-01 g/l ALOGPS
logP -1.6 ChemAxon
IUPAC Name (2R)-2,4-dihydroxy-3,3-dimethyl-N-(2-{[(E)-2-sulfanylethenyl]carbamoyl}ethyl)butanamide ChemAxon
Traditional IUPAC Name pantothenoylaminoethenethiol ChemAxon
Molecular Weight 276.353 ChemAxon
Monoisotopic Weight 276.114377828 ChemAxon
Molecular Formula C11H20N2O4S ChemAxon
InChI InChI=1S/C11H20N2O4S/c1-11(2,7-14)9(16)10(17)13-4-3-8(15)12-5-6-18/h5-6,9,14,16,18H,3-4,7H2,1-2H3,(H,12,15)(H,13,17)/b6-5+/t9-/m0/s1 ChemAxon
Polar Surface Area (PSA) 98.66 ChemAxon
Refractivity 70.12 ChemAxon
Polarizability 28.69 ChemAxon
Rotatable Bond Count 7 ChemAxon
H Bond Acceptor Count 4 ChemAxon
H Bond Donor Count 5 ChemAxon
pKa (strongest acidic) 8.47 ChemAxon
pKa (strongest basic) -2.8 ChemAxon
Physiological Charge 0 ChemAxon
Number of Rings 0 ChemAxon
Bioavailability 1 ChemAxon
Rule of Five 1 ChemAxon
Ghose Filter 0 ChemAxon
MDDR-Like Rule 0 ChemAxon

Target within organism

  • Phosphopantothenoylcysteine decarboxylase : in Human