CAS 471-87-4|Stachydrine

Introduction:Basic information about CAS 471-87-4|Stachydrine, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameStachydrine
CAS Number471-87-4Molecular Weight143.18
Density1.1095 (rough estimate)Boiling Point261.28°C (rough estimate)
Molecular FormulaC7H13NO2Melting Point235°C
MSDS/Flash Point/

Names

NameL-proline betaine
SynonymMore Synonyms

Stachydrine BiologicalActivity

DescriptionStachydrine is a major constituent of Chinese herb leonurus heterophyllus sweet used to promote blood circulation and dispel blood stasis. Stachydrine can inhibit the NF-κB signal pathway.
Related CatalogResearch Areas >>Cardiovascular DiseaseNatural Products >>Others
Target

p65

Human Endogenous Metabolite

In VitroStachydrine can inhibit the NF-κB signal pathway, and this may be related to the mechanism of anti-hypertrophic. Intervention of stachydrine significantly suppresses the level of p-IκB protein in the cytosol and NF-κB protein in the nucleus [1]. Tissue factor mRNA is decreased in stachydrine-treated human umbilical vein endothelial cells. Stachydrine attenuates the decline of human umbilical vein endothelial cells viability and the increase of LDH activity induced by anoxia-reoxygenation[2]. A dose dependent decrease in expression of mRNA, and protein levels are observed in stachydrine-treated human prostate cancer cells (PC-3 and LNcaP)[3].
In VivoStachydrine attenuates norepinephrine-induced cardiomyocyte hypertrophy and has potential protective effects against β-adrenergic receptor induced Ca2+ mishandling[4]. Stachydrine treatment reduces the expressions of PERK, CHOP, and caspase-3 in the endoplasmic reticulum stress-related apoptosis pathway[5].
Cell AssayCytotoxicity is determined by colorimetric MTT cleavage assay. Briefly, human umbilical vein endothelial cells (HUVECs) are plated in triplicate in 96-well culture plates, and treated with different final concentrations (0.01, 0.1, 1, 10, 100 μM) of stachydrine respectively for 24 hours. After incubation, culture media are discarded and new culture media containing 0.5mg/mL of MTT are added. The plates are further incubated at 37°C for 4 hours. After the incubation, culture media are discarded and 0.1 mL of dimethyl sulfoxide (DMSO) is added to each well to solubilize the formazine crystals. The absorbance (OD) is measured at 540 nm using a microplate reader[3].
Animal AdminRats: Ventricular myocytes from 1-day-old Wistar rats are isolated and cultured in DMEM/F12 with 1 μM norepinephrine in the presence or absence of 10 μM stachydrine for 72 h. Cardiomyocytes hypertrophy is evaluated by cell surface area, total protein/DNA content, β/α-MHC mRNA ratio. While calcium handling function is evaluated by Ca2+-transient amplitude and decay, SERCA2a activity and expression, PLN expression and phosphorylation. β1-adrenergic receptor system activation is evaluated by the content of cAMP and the activation of PKA[5].
References

[1]. Guo W, et al. Effect of Leonurus stachydrine on myocardial cell hypertrophy. Zhong Yao Cai. 2012 Jun;35(6):940-3.

[2]. Yin J, et al. Stachydrine, a major constituent of the Chinese herb leonurus heterophyllus sweet, ameliorates human umbilical vein endothelial cells injury induced by anoxia-reoxygenation. Am J Chin Med. 2010;38(1):157-71.

[3]. Rathee P, et al. In vitro anticancer activity of stachydrine isolated from Capparis decidua on prostate cancer cell lines. Nat Prod Res. 2012;26(18):1737-40.

[4]. Zhang C, et al. Effects of stachydrine on norepinephrine-induced neonatal rat cardiac myocytes hypertrophy and intracellular calcium transients. BMC Complement Altern Med. 2014 Dec 8;14:474.

[5]. Zhang C, et al. Effect of stachydrine on endoplasmic reticulum stress-induced apoptosis in rat kidney after unilateral ureteral obstruction. J Asian Nat Prod Res. 2013;15(4):373-81.

Chemical & Physical Properties

Density1.1095 (rough estimate)
Boiling Point261.28°C (rough estimate)
Melting Point235°C
Molecular FormulaC7H13NO2
Molecular Weight143.18
PSA37.30000
LogP-2.97
Index of Refraction1.4150 (estimate)
InChIKeyCMUNUTVVOOHQPW-LURJTMIESA-N
SMILESC[N+]1(C)CCCC1C(=O)[O-]
Storage condition-20°C

Safety Information

HS Code29214980

Customs

HS Code29214980

Synonyms

proline betaine
stachydrine
N,N-Dimethyl-L-proline
Stachydrine hydrochloride
Methyl hygrate betaine
L-Proline betaine
(S)-2-Carboxy-1,1-dimethylpyrrolidinium Hydroxide Inner Salt
1-Methylproline methylbetaine
Pyrrolidinium, 2-carboxy-1,1-dimethyl-, inner salt, (2S)-
Cadabine
methyl hygrate βine
Hygric Acid Methylbetaine
(2S)-1,1-Dimethyl-2-pyrrolidiniumcarboxylate
1,1-dimethylpyrrolidinium-2-carboxylate
(S)-1,1-Dimethylpyrrolidin-1-ium-2-carboxylate
(2S)-1,1-Dimethylpyrrolidinium-2-carboxylate
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