| Weight | 189.214 g/mol |
|---|---|
| Formula | C11H11NO2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
3-Indolepropionic acid (830-96-6)
indolepropionic acid · indole propionate · indole-3-propanoic acid
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- Indole-3-propionate: A potent hydroxyl radical scavenger in rat brain (Brain Research, 1999)
- Spectroscopy of complexes of tryptamine and 3-indolepropionic acid with various solvents (The Journal of Physical Chemistry, 1988)
- The Origin of Indoleacetic Acid and Indolepropionic Acid in Rat and Human Cerebrospinal Fluid (Journal of Neurochemistry, 1980)
- The structure of trp pseudorepressor at 1.65 shows why indole propionate acts as a trp 'inducer' (Nature, 1988)
- Preparation, structure and discrimination of a chiral bimolecular crystal by the self-assembly of 3-indolepropionic acid and phenanthridine (Tetrahedron Letters, 1997)
- Meldrum's Acid in Organic Synthesis. V. Versatile One-pot Synthesis of Indolepropionic Esters via Simultaneous Condensation of Three Different Carbon Components, Indole, Aldehydes and Meldrum's Acid (Chemical & Pharmaceutical Bulletin, 1982)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - indolepropionic acid
- indole propionate
- indole-3-propanoic acid
-
SMILESC1=CC=C2C(=C1)C(=CN2)CCC(=O)O
-
InChIKeyGOLXRNDWAUTYKT-UHFFFAOYSA-N
- Pubchem - 3-Indolepropionic acid
- Wikipedia - 3-indolepropionic acid
3-Indolepropionic acid (IPA), or indole-3-propionic acid, is a potent neuroprotective antioxidant and plant auxin that is being studied for therapeutic use in Alzheimer's disease. It is endogenously produced by human microbiota and has only been detected in vivo when the species Clostridium sporogenes is present in the gastrointestinal tract. As of April 2016, C.
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3-Indolepropionic acid
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