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3-Indoleacrylic acid

Names

[ CAS No. ]:
1204-06-4

[ Name ]:
3-Indoleacrylic acid

[Synonym ]:
3-(3-Indolyl)acrylic acid,IAA
2-Propenoic acid, 3-(1H-indol-2-yl)-, (2E)-
3-(3-Indolyl)acrylic acid IAA
(2E)-3-(1H-Indol-2-yl)acrylic acid
2-Propenoic acid,3-(1H-indol-3-yl)-
3-Indolylacrylic acid
3-Indoleacrylic Acid
3-(3-Indolyl)acrylic Acid
EINECS 214-872-7
MFCD00005633
(E)-3-(indol-2-yl)acrylic acid
3-(1H-Indol-3-yl)acrylic acid

Biological Activity

[Description]:

3-Indoleacrylic acid is a high-efficient antialgal agent. 3-Indoleacrylic acid increases reactive oxygen species (ROS) production, and inhibits the functions of all the nutrient assimilating genes, down-regulated ribulose-1,5-bisphosphate carboxylase/oxygenase II, and cytochrome f genes in P. donghaiense[1].

[Related Catalog]:

Research Areas >> Others

[References]

[1]. Kokoette Effiong, et al. 3-Indoleacrylic acid from canola straw as a promising antialgal agent - Inhibition effect and mechanism on bloom-forming Prorocentrum donghaiense. Mar Pollut Bull. 2022 May:178:113657.  

Chemical & Physical Properties

[ Density]:
1.4±0.1 g/cm3

[ Boiling Point ]:
432.8±20.0 °C at 760 mmHg

[ Melting Point ]:
180-186ºC

[ Molecular Formula ]:
C11H9NO2

[ Molecular Weight ]:
187.195

[ Flash Point ]:
215.6±21.8 °C

[ Exact Mass ]:
187.063324

[ PSA ]:
53.09000

[ LogP ]:
2.34

[ Vapour Pressure ]:
0.0±1.1 mmHg at 25°C

[ Index of Refraction ]:
1.750

[ Storage condition ]:
0-6°C

[ Water Solubility ]:
freely soluble

MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
NL3680000
CHEMICAL NAME :
Indole-3-acrylic acid
CAS REGISTRY NUMBER :
1204-06-4
BEILSTEIN REFERENCE NO. :
0006317
LAST UPDATED :
199701
DATA ITEMS CITED :
6
MOLECULAR FORMULA :
C11-H9-N-O2
MOLECULAR WEIGHT :
187.21
WISWESSER LINE NOTATION :
T56 BMJ D1U1VQ

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
1600 mg/kg/8W-I
TOXIC EFFECTS :
Tumorigenic - Carcinogenic by RTECS criteria Kidney, Ureter, Bladder - tumors
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - guinea pig
DOSE/DURATION :
1100 mg/kg/13W-I
TOXIC EFFECTS :
Tumorigenic - equivocal tumorigenic agent by RTECS criteria Gastrointestinal - tumors Blood - leukemia
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - hamster
DOSE/DURATION :
1600 mg/kg/10W-I
TOXIC EFFECTS :
Tumorigenic - neoplastic by RTECS criteria Endocrine - adrenal cortex tumors Blood - tumors

MUTATION DATA

TEST SYSTEM :
Primate - monkey
DOSE/DURATION :
15 mg/kg/2D (Intermittent)
REFERENCE :
TSITAQ Tsitologiya. Cytology. (V/O Mezhdunarodnaya Kniga, 113095 Moscow, USSR) V.1- 1959- Volume(issue)/page/year: 15,1505,1973

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ RTECS ]:
NL3680000

[ HS Code ]:
2933990090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2933990090

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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Structural insight into the inhibition of human kynurenine aminotransferase I/glutamine transaminase K.

J. Med. Chem. 52 , 2786-93, (2009)

Human kynurenine aminotransferase I (hKAT I) catalyzes the formation of kynurenic acid, a neuroactive compound. Here, we report three high-resolution crystal structures (1.50-1.55 A) of hKAT I that ar...

NMR studies of the mode of binding of corepressors and inducers to Escherichia coli trp repressor.

Eur. J. Biochem. 235(3) , 804-13, (1996)

The binding of the corepressors tryptophan and 5-methyltryptophan and of the inducers 3-indolepropionate, 3-indoleacrylate and 5-methylindole to the Escherichia coli trp repressor have been studied by...


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Related Compounds

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