CAS 392-12-1

Indole-3-pyruvic acid

Description:

Indole-3-pyruvic acid (IPA) is an organic compound that belongs to the class of indole derivatives, characterized by its structure which includes an indole ring and a pyruvic acid moiety. It is a naturally occurring compound found in various plants and is known for its role as a precursor in the biosynthesis of auxins, which are essential plant hormones that regulate growth and development. IPA is typically a white to off-white crystalline solid, soluble in water and organic solvents, and exhibits a melting point that varies depending on purity. The compound has garnered interest in research due to its potential applications in agriculture and medicine, particularly in plant growth regulation and as a possible therapeutic agent. Its biological activities include antioxidant properties and potential effects on cellular signaling pathways. As with many organic compounds, IPA should be handled with care, following appropriate safety guidelines to mitigate any risks associated with its use.

Formula: C₁₁H₉NO₃

InChI: InChI=1S/C11H9NO3/c13-10(11(14)15)5-7-6-12-9-4-2-1-3-8(7)9/h1-4,6,12H,5H2,(H,14,15)

InChI key: InChIKey=RSTKLPZEZYGQPY-UHFFFAOYSA-N

SMILES: C(C(C(O)=O)=O)C=1C=2C(NC1)=CC=CC2

Synonyms:

• 1H-Indole-3-propanoic acid, α-oxo-
• 1H-Indole-3-pyruvic acid
• 3-(1H-indol-3-yl)-2-oxopropanoate
• 3-(1H-indol-3-yl)-2-oxopropanoic acid
• 3-(3-Indolyl)-2-Oxopropanoic Acid
• 3-(3-Indolyl)pyruvic acid
• 3-Indolylpyroracemic acid
• 3-Indolylpyruvic acid
• 5-Iodophthalide
• Indole-3-(2-Oxo)-Propanoic Acid
• Indole-3-Pyruvic Acid Monohydrate
• Indole-3-pyruvate
• Indolepyruvic acid
• Indolyl-3-pyruvate
• NSC 88874
• Pol 240
• alpha-Oxo-1H-indole-3-propanoic acid
• α-Oxo-1H-indole-3-propanoic acid
• β-Indolepyruvic acid
• β-Indolylpyruvic acid

Indole-3-pyruvic acid

CAS: 392-12-1

3-(1H-Indol-3-yl)-2-oxopropanoic acid

Formula: C₁₁H₉NO₃

Purity: 95%

Molecular weight: 203.19

Ref: IN-DG13725

3-(1H-indol-3-yl)-2-oxopropanoic acid

CAS: 392-12-1

Formula: C₁₁H₉NO₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 203.1941

Ref: IN-DA003HZC

Indole-3-pyruvic acid

CAS: 392-12-1

Indole-3-pyruvic acid

Formula: C₁₁H₉NO₃

Color and Shape: Yellow Solid-Powder

Molecular weight: 203.19406

Ref: 54-BIB6079

Indole-3-pyruvic acid

CAS: 392-12-1

Ref: 7W-GK3116

3-(1H-indol-3-yl)-2-oxopropanoic acid

CAS: 392-12-1

3-(1H-indol-3-yl)-2-oxopropanoic acid

Formula: C₁₁H₉NO₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 203.19406

Ref: 54-OR24640

Indole-3-pyruvic acid

CAS: 392-12-1

Indole-3-pyruvic acid

Formula: C₁₁H₉NO₃

Purity: ≥98%

Molecular weight: 203.19

Ref: 54-BUP16180

Indole-3-pyruvic acid

CAS: 392-12-1

Indole-3-pyruvic acid is a precursor for the plant growth hormone indole-3-acetic acid.

Formula: C₁₁H₉NO₃

Purity: 98.08% - 99.21%

Color and Shape: Yellow Solid

Molecular weight: 203.19

Ref: TM-T4939

Indole-3-pyruvic Acid

CAS: 392-12-1

Applications Indole-3-pyruvic Acid is a compound involved in the biosynthesis of Indole-3-acetic acid, a plant hormone which plays important roles in regulating growth and responses to environmental changes.
References Kong, W., et al.: Plant Cell Physiol, 56, 715-726 (2015)

Formula: C₁₁H₉NO₃

Color and Shape: Neat

Molecular weight: 203.19

Ref: TR-I627180

Indole-3-pyruvic acid

CAS: 392-12-1

Thiostrepton is an antibiotic that inhibits the synthesis of proteins by binding to the α subunit of the bacterial ribosome. It also has a polymerase chain reaction (PCR) amplification activity. Thiostrepton's inhibitory effect on protein synthesis is due to its ability to bind to the α subunit of the ribosome, which results in inhibition of enzyme activities and physiological function. The thiostrepton-resistant mutants have been found in skin cells and plants. The resistant mutants are mostly due to point mutations in amino acid residues on the surface of the ribosomal target site, which alters its affinity for thiostrepton. This antibiotic has been shown to be active against wild-type strains of bacteria, as well as methicillin-resistant Staphylococcus aureus (MRSA). Thiostrepton's active form is metabolized through hydroxylation and conjugation with glutathione or glucur

Formula: C₁₁H₉NO₃

Purity: Area-% Min. 95 Area-%

Color and Shape: Off-White Yellow Powder

Molecular weight: 203.20 g/mol

Ref: 3D-FI30479

3-(1H-Indol-3-yl)-2-oxopropanoic acid

CAS: 392-12-1

Formula: C₁₁H₉NO₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 203.197

Ref: 10-F210523