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487-79-6

487-79-6 structure
487-79-6 structure
  • Name: Kainic acid
  • Chemical Name: kainic acid
  • CAS Number: 487-79-6
  • Molecular Formula: C10H15NO4
  • Molecular Weight: 213.230
  • Catalog: Research Areas Neurological Disease
  • Create Date: 2018-05-12 08:00:00
  • Modify Date: 2024-01-02 20:35:45
  • Kainic acid is a potent agonist at excitatory amino acid receptor subtypes in the CNS.

Name kainic acid
Synonyms KAINATE
helminal
kainic acid
Kainic
digenin
Dihydroergocristine mesylate
(3S,4S)-3-(Carboxymethyl)-4-isopropenyl-L-proline
digenicacid
(−)-Kainic Acid
L-Proline, 3-(carboxymethyl)-4-(1-methylethenyl)-, (3S,4S)-
Description Kainic acid is a potent agonist at excitatory amino acid receptor subtypes in the CNS.
Related Catalog
In Vivo Kainic acid is a potent agonist at excitatory amino acid receptor subtypes in the CNS. HO-I levels are significantly enhanced one, three and seven days after i.c.v, injection of Kainic acid. One day after i.c.v, injection of Kainic acid, the HO-I protein level reaches a maximum and then decreases, but is still significantly enhanced versus the vehicle-injected group. After i.c.v. injection of Kainic acid, HO-I-immunoreactivity is strongly induced not only in the CA3 but also widely in the whole hippocampus[1].
Animal Admin The rats are fasted over night with free access to water. For stereotaxic injection, rats are anaesthetized (sodium pentobarbital, 50 mg/kg, i.p.) and immobilized in a Kopf stereotaxic frame. The rats are microinjected with 1 μg Kainic acid in 2 μL of sterilized physiological saline into the right lateral ventricle, i.e., 0.2 mm caudal from the bregma, 1.2 mm right lateral and 3.8 mm ventral according to the rat brain atlas. For control, rats are injected with same amount (2 μL) of vehicle, sterilized physiological saline. Five rats in each group are used in this study[1].
References

[1]. Matsuoka Y, et al. Kainic acid induction of heme oxygenase in vivo and in vitro. Neuroscience. 1998 Aug;85(4):1223-33.

Density 1.2±0.1 g/cm3
Boiling Point 439.9±45.0 °C at 760 mmHg
Melting Point 253-254ºC
Molecular Formula C10H15NO4
Molecular Weight 213.230
Flash Point 219.8±28.7 °C
Exact Mass 213.100113
PSA 86.63000
LogP 0.50
Vapour Pressure 0.0±2.3 mmHg at 25°C
Index of Refraction 1.509
Storage condition 2-8℃

CHEMICAL IDENTIFICATION

RTECS NUMBER :
UX9665250
CHEMICAL NAME :
3-Pyrrolidineacetic acid, 2-carboxy-4-isopropenyl-
CAS REGISTRY NUMBER :
487-79-6
BEILSTEIN REFERENCE NO. :
0086660
LAST UPDATED :
199709
DATA ITEMS CITED :
5
MOLECULAR FORMULA :
C10-H15-N-O4
MOLECULAR WEIGHT :
213.26

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LDLo - Lowest published lethal dose
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
32 mg/kg
TOXIC EFFECTS :
Brain and Coverings - other degenerative changes Behavioral - somnolence (general depressed activity) Behavioral - convulsions or effect on seizure threshold
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Subcutaneous
DOSE :
3 mg/kg
SEX/DURATION :
female 14 day(s) after conception
TOXIC EFFECTS :
Reproductive - Effects on Newborn - growth statistics (e.g.%, reduced weight gain) Reproductive - Effects on Newborn - behavioral
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Subcutaneous
DOSE :
3 mg/kg
SEX/DURATION :
female 17-18 day(s) after conception
TOXIC EFFECTS :
Reproductive - Effects on Newborn - growth statistics (e.g.%, reduced weight gain) Reproductive - Effects on Newborn - behavioral
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Subcutaneous
DOSE :
3 mg/kg
SEX/DURATION :
female 19 day(s) after conception
TOXIC EFFECTS :
Reproductive - Effects on Newborn - growth statistics (e.g.%, reduced weight gain)

MUTATION DATA

TEST SYSTEM :
Rodent - mouse
DOSE/DURATION :
12 mg/kg
REFERENCE :
FOBGA8 Folia Biologica (Krakow). (Ars Polona, POB 1001, 00-068 Warsaw 1, Poland) V.1- 1953- Volume(issue)/page/year: 36,103,1988
Hazard Codes Xn
Risk Phrases R20/21/22
Safety Phrases 22-24/25-36
RTECS UX9665250