Basic information
- Standard SMILES
O=C(O)CCc1c[nH]c2ccccc12- InChIKey
GOLXRNDWAUTYKT-UHFFFAOYSA-N- Molecular formula
- C11H11NO2
- Average molar mass
- 189.21 g/mol
- Monoisotopic mass
- 189.07897859
Overview
3-(1H-indol-3-yl)propanoic acid is an indol-3-yl carboxylic acid that is propionic acid substituted by a 1H-indol-3-yl group at position 3. It has a role as an auxin, a plant metabolite and a human metabolite. It is functionally related to a propionic acid. It is a conjugate acid of a 3-(1H-indol-3-yl)propanoate.
Names & identifiers
- Preferred name
- 1H-Indole-3-propanoic acid
- IUPAC
- 3-(1H-indol-3-yl)propanoic acid
- English name
- 3-Indolepropionic acid
- Molecular formula
- C11H11NO2
- Molecular weight
- 189.21
Names & synonyms
Show more names
Database identifiers
- CAS
830-96-6- PubChem CID
- 3744
- DTXSID
DTXSID7061192- ChEMBL
CHEMBL207225- ChEBI
CHEBI:43580- UNII
- JF49U1Q7KN
- EC Number
- 212-600-1
- Nikkaji
- J7.131E
Properties
Computed structural properties
- XLogP
- 1.8
- Topological polar surface area
- 53.1 Ų
- Hydrogen bond donors
- 2
- Hydrogen bond acceptors
- 2
- Rotatable bonds
- 3
- Heavy atoms
- 14
- Formal charge
- 0
- Complexity
- 217
Experimental & physicochemical properties
Physicochemical properties
- Melting point
- 133 °C · ~133 °C
- Boiling point
- 82 °C · 82 °C(lit.)
- Density
- 0.96 g/mL · 0.960 g/mL at 20 °C
- vapor density
- 2.1 · 2.1 (vs air)
- vapor pressure
- 33 mm · 33 mm Hg ( 20 °C)
- refractive index
- 20 · n20/D 1.377(lit.)
- Flash point
- 53 °F · 53 °F
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- 50 mg/mL, · ethanol: soluble50mg/mL, clear, yellow to orange
- pka
- 4.77 · 4.77±0.10(Predicted)
- form
- crystalline
- color
- light yellow
- Water Solubility
- slightly soluble
- BRN
- 147733 · 147733
- InChI
- 1S/C11H11NO2/c13-11(14)6-5-8-7-12-10-4-2-1-3-9(8)10/h1-4,7,12H,5-6H2,(H,13,14)
- InChIKey
- GOLXRNDWAUTYKT-UHFFFAOYSA-N
- SMILES
- OC(=O)CCc1c[nH]c2ccccc12
- CAS DataBase Reference
- 830 · 830-96-6(CAS DataBase Reference)
- EWG's Food Scores
- 1 · 1
- FDA UNII
- 49 U1Q7KN · JF49U1Q7KN
- NIST Chemistry Reference
- -3 · Indole-3-propionic acid(830-96-6)
- EPA Substance Registry System
- 1 H-Indole-3-propanoic · 1H-Indole-3-propanoic acid (830-96-6)
- UNSPSC Code
- 12352106 · 12352106
- NACRES
- 77 · NA.77
- Symbol(GHS)
- 7 · GHS07
- Signal word
- Warning
- Hazard statements
- 315 · H315-H319-H335
- Precautionary statements
- 261 · P261-P280a-P304+P340-P305+P351+P338-P405-P501a
- PPE
- 95 · Eyeshields, Gloves, type N95 (US)
- Hazard Codes
- Xi
- Risk Statements
- 22 · 22-36/37/38
- Safety Statements
- 26 · 26-37/39
- WGK Germany
- 3 · 3
- RTECS
- 1329000 · NM1329000
- F
- 8 · 8-10-23
- TSCA
- TSCA listed
- HS Code
- 29339990 · 29339990
- Storage Class
- 11 · 11 - Combustible Solids
- Toxicity
- 100 mg/kg · LDLo intraperitoneal in mouse: 100mg/kg
Safety & regulation
GHS classification
GHS Classification
This chemical does not meet GHS hazard criteria for 18.2% (2 of 11) of reports.
Warning
H302 (18.2%): Harmful if swallowed [Warning Acute toxicity, oral]
P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 11 reports by companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard information
Safety data
- F
- 8-10-23
- PPE
- Eyeshields, Gloves, type N95 (US)
- wgk
- 3
- tsca
- TSCA listed
- rtecs
- NM1329000
- hs_code
- 29339990
- Toxicity
- LDLo intraperitoneal in mouse: 100mg/kg
- risk_code
- 22-36/37/38
- Signal word
- Warning
- Symbol(GHS)
- GHS07
- hazard_code
- Xi
- safety_code
- 26-37/39
- Storage Class
- 11 - Combustible Solids
- Hazard statements
- H315-H319-H335
- Precautionary statements
- P261-P280a-P304+P340-P305+P351+P338-P405-P501a
Chemistry & industry
Pharmacology
Uses & manufacturing
Applications
Description3-Indolepropionic acid is a bacterial metabolite that has antioxidant and neuroprotective activities. It scavenges ABTS radicals in a cell-free assay when used at concentrations ranging from 50 to 150 μM and decreases hydrogen peroxide-induced malondialdehyde (MDA) levels in rat striatal membranes (IC50 = 180 μM). Indole-3-propionic acid also decreases increases in MDA levels induced by amyloid β (1-42) in PC12 cells. It decreases ischemia-induced increases in cell death of pyramidal neurons and levels of 4-hydroxy nonenal (HNE; ) and glial fibrillary acidic protein (GFAP) in the hippocampal CA1 region in gerbils when administered at a dose of 10 mg/kg per day.
Uses3-Indolepropionic acid is a deamination product of Tryptophan (T947200) that protects the hippocampus (studied in gerbils) from ischemic damage and oxidative stress. It’s ability to protect the neurons in this way is attributed to its potent antioxidative effects. 3-Indolepropionic acid is also hypothesized to have protective effects on the thyroid gland.
UsesReactant for preparation of:Fluorescent analogues of strigolactonesAnti-tumor agentsMelanocortin receptors ligandsImmunosuppressive agentsIinhibitors of hepatitis C virusHistamine H4 receptor agonistsNR2B/NMDA receptor antagonistsCB1 antagonist for the treatment of obesityAntibacterial agentsInhibitor of TGF-β receptor bindingIndole-3-propionic acid may be used in the synthesis of oxindole-3-propionic acid via reaction with N-bromosuccinimide in acetic acid followed by treatment with H2/Pd catalyst.
General Description3-Indolepropionic acid is an effective inhibitor of aggregation of misfolded β-amyloid protein (Abeta). Three-component one-pot procedure has been reported to assemble 3-indolepropionic acids.
Upstream & downstream products
Upstream raw materials
Downstream products
Suppliers50 total
Additional notes
DefinitionChEBI: An indol-3-yl carboxylic acid that is propionic acid substituted by a 1H-indol-3-yl group at position 3.
Related reactions
Linked notes
Loading…