goralatide

Modify Date: 2024-01-02 17:09:25

goralatide structure	Common Name	goralatide
	CAS Number	127103-11-1	Molecular Weight	487.504
	Density	1.4±0.1 g/cm3	Boiling Point	992.0±65.0 °C at 760 mmHg
	Molecular Formula	C₂₀H₃₃N₅O₉	Melting Point	N/A
	MSDS	N/A	Flash Point	553.7±34.3 °C

Use of goralatide

N-Acetyl-Ser-Asp-Lys-Pro is a natural and specific substrate for the N-terminal site of ACE.

Name	1-[2-[[2-[(2-acetamido-3-hydroxypropanoyl)amino]-3-carboxypropanoyl]amino]-6-aminohexanoyl]pyrrolidine-2-carboxylic acid
Synonym	More Synonyms

Description	N-Acetyl-Ser-Asp-Lys-Pro is a natural and specific substrate for the N-terminal site of ACE.
Related Catalog	Signaling Pathways >> Metabolic Enzyme/Protease >> Angiotensin-converting Enzyme (ACE) Research Areas >> Cardiovascular Disease Research Areas >> Inflammation/Immunology Peptides
In Vitro	N-Acetyl-Ser-Asp-Lys-Pro is an endogenous tetrapeptide secreted by bone marrow and is ubiquitously found in plasma and various tissues. N-Acetyl-Ser-Asp-Lys-Pro is degraded specifically by ACE, and its plasma level rises substantially during ACE inhibitor therapy. N-Acetyl-Ser-Asp-Lys-Pro inhibits the proliferation of isolated cardiac fibroblasts but significantly stimulates the proliferation of vascular smooth muscle cells. Flow cytometry of rat cardiac fibroblasts treated with N-Acetyl-Ser-Asp-Lys-Pro shows significant inhibition of the progression of cells from G0/G1 phase to S phase of the cell cycle. In cardiac fibroblasts transfected with a Smad-sensitive luciferase reporter construct, N-Acetyl-Ser-Asp-Lys-Pro decreases luciferase activity by 55%. Moreover, phosphorylation and nuclear translocation of Smad2 is decreased in cardiac fibroblasts treated with N-Acetyl-Ser-Asp-Lys-Pro[1]. N-acetyl-seryl-aspartyl-lysyl-proline is a negative regulator of hematopoietic stem cell proliferation. N-acetyl-seryl-aspartyl-lysyl-proline is involved in the control of hematopoietic stem cell proliferation by preventing their recruitment into S-phase. N-acetyl-seryl-aspartyl-lysyl-proline appears to exert this function by blocking the action of a stem cell-specific proliferation stimulator and acts selectively on quiescent progenitors[2]. N-Acetyl-Ser-Asp-Lys-Pro inhibits collagenase expression and activation is associated with increased expression of TIMP-1 and TIMP-2. N-Acetyl-Ser-Asp-Lys-Pro does not alter collagenase or gelatinase activity in cardiac fibroblasts under basal conditions, but blunts the IL-1β-induced increase in total collagenase activity. Similarly, N-Acetyl-Ser-Asp-Lys-Pro normalizes the IL-1β-mediated increase in MMP-2 and MMP-9 activities and MMP-13 expression[3].
In Vivo	N-Acetyl-Ser-Asp-Lys-Pro prevents hypertension-induced inflammatory cell infiltration, collagen deposition, nephrin downregulation and albuminuria, which could lead to renoprotection in hypertensive mice[4].
Kinase Assay	The kinetics of N-Acetyl-Ser-Asp-Lys-Pro hydrolysis are determined by incubating enzymes (0.4 nM wild-type ACE, 0.3 nM ACE K959 963, and 9 nM ACE K361 365) with N-Acetyl-Ser-Asp-Lys-Pro over a concentration range of 0.35-40 μM, added to [3H]N-Acetyl-Ser-Asp-Lys-Pro (5 μCi). The reaction is stopped by freezing on dry ice, and samples are then analyzed[2].
Animal Admin	Mice: 16-week-old C57BL/6J mice are treated with either placebo, DCOA (10 mg/10 g body weight subcutaneous) and 1% sodium chloride with 0.2% potassium chloride in drinking water (DOCA-salt) or DOCA-salt with Ac-SDKP (800 μg/kg per day) for 12 weeks. Bloof pressure, urine albumin, glomerular matrix, renal collagen content, monocyte/macrophage infiltration and glomerular nephrin expression are measured[4].
References	[1]. Rousseau A, et al. The hemoregulatory peptide N-acetyl-Ser-Asp-Lys-Pro is a natural and specificsubstrate of the N-terminal active site of human angiotensin-converting enzyme. J Biol Chem. 1995 Feb 24;270(8):3656-61. [2]. Pokharel S, et al. N-acetyl-Ser-Asp-Lys-Pro inhibits phosphorylation of Smad2 in cardiac fibroblasts. Hypertension. 2002 Aug;40(2):155-61. [3]. Rhaleb NE, et al. N-acetyl-Ser-Asp-Lys-Pro inhibits interleukin-1β-mediated matrix metalloproteinase activation in cardiac fibroblasts. Pflugers Arch. 2013 Oct;465(10):1487-95. [4]. Rhaleb NE, et al. Renal protective effects of N-acetyl-Ser-Asp-Lys-Pro in deoxycorticosterone acetate-salt hypertensive mice. J Hypertens. 2011 Feb;29(2):330-8.

Density	1.4±0.1 g/cm3
Boiling Point	992.0±65.0 °C at 760 mmHg
Molecular Formula	C₂₀H₃₃N₅O₉
Molecular Weight	487.504
Flash Point	553.7±34.3 °C
Exact Mass	487.227814
PSA	238.93000
LogP	-1.91
Appearance of Characters	Solid \| White to off-white
Vapour Pressure	0.0±0.6 mmHg at 25°C
Index of Refraction	1.565
Storage condition	−20°C
Water Solubility	Soluble in water at 2mg/ml

goralatide MSDS(Chinese)

WGK Germany	3

NAcSer(OBzl)DAsp(OBzl)Lys(Z)ProOBzl structure

NAcSer(OBzl)DAs...

CAS#:127129-86-6

~%

goralatide Structure

goralatide

CAS#:127103-11-1

Literature: Journal of Medicinal Chemistry, , vol. 33, # 8 p. 2122 - 2127

1-acetylimidazole structure

1-acetylimidazole

CAS#:2466-76-4

~%

goralatide Structure

goralatide

CAS#:127103-11-1

Literature: Journal of Medicinal Chemistry, , vol. 33, # 8 p. 2122 - 2127

BocS(OBzl)-D-D(OBzl)K(Z)P-OBzl structure

BocS(OBzl)-D-D(...

CAS#:127103-29-1

~%

goralatide Structure

goralatide

CAS#:127103-11-1

Literature: Journal of Medicinal Chemistry, , vol. 33, # 8 p. 2122 - 2127

Precursor 3
CAS#:127129-86-6 NAcSer(OBzl)DAs... CAS#:2466-76-4 1-acetylimidazole CAS#:127103-29-1 BocS(OBzl)-D-D(...
DownStream 0

goralatide

L-Proline, N-acetyl-L-seryl-L-α-aspartyl-L-lysyl-

Acetyl-Ser-Asp-Lys-Pro

NAcSerDAspLysPro

N-Acetyl-L-seryl-L-α-aspartyl-L-lysyl-L-proline

MFCD00133611

1-(N2-(N-(N-Acetyl-L-seryl)-L-a-aspartyl)-L-lysyl)-L-proline

Ac-Ser-Asp-Lys-Pro-OH

Thymosin β4 (1-4)

N-Acetyl-Ser-Asp-Lys-Pro

Zhejiang Hangyu API Co., Ltd
China
Product Name: Goralatide
Price: $Inquiry/1kg
Purity: 99.0%
Stocking Period: 1 Day
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Price: $60/1mg

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