1H-Indole-3-propanoic acid

HCID 3744CAS 830-96-6

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

3-Indolepropionic acid830-96-6Indole-3-propionic acid1H-Indole-3-propanoic acidIndolepropionic acid3-(3-Indolyl)propionic acid3-(3-Indolyl)propanoic acidOxigon3-(Indol-3-yl)propionic acid1H-INDOLE-3-PROPIONIC ACID3-(3-Indole)propionic acidbeta-(3-Indolyl)propionic acid
Show more names
PROPAN-2-OL3-(1H-INDOL-3-YL)PROPANOIC ACIDISOPROPYL ALCOHOISOPROPANEFEMA 2929ISOPROPANOISOPROPANOL ALCOHOL2-PPROPANOL
3-Indolepropionicacidindole-3-propanoic acidJF49U1Q7KN1H-Indole-3-proponoic acidVP-20629NSC-3252NSC-47831SHP622

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

Experimental & physicochemical properties

DrugsPharmaceuticals -> Listed in ZINC15
LogP1.75
Melting Point134 - 135 °C
Physical DescriptionSolid

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.)

Safety & regulation

GHS classification

GHS Classification · 5 items

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

Regulatory Information1H-Indole-3-propanoic acid: Does not have an individual approval but may be used under an appropriate group standard
Hazard Classes and CategoriesAcute Tox. 4 (18.2%)

Safety data

F
8-10-23
PPE
Eyeshields, Gloves, type N95 (US)
wgk
3
tsca
TSCA listed
rtecs
NM1329000
hs_code
29339990

Chemistry & industry

Pharmacology

Cellular LocationsMembrane

Uses & manufacturing

General Manufacturing Information1H-Indole-3-propanoic acid: INACTIVE
Applications · 4 items

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.

Suppliers50 total

国药集团化学试剂有限公司86-21-63210123 · [email protected]
梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
INTATRADE GmbH+49 3493/605464 · [email protected]
韶远科技(上海)有限公司021-50795510 4000665055 · [email protected]

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

63 records

Linked notes

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