26 Results for "

endothelin-1 (ET-1)

" in MedChemExpress (MCE) Product Catalog:
Products (26)

26 Results for "endothelin-1 (ET-1)" in MCE Product Catalog:

12
12 Publications Verification
Cat. No.: HY-113046
CAS No.: 134-35-0
Purity:  99.77%
Synonyms: 5-Methyl THF; 5-MTHF
5-Methyltetrahydrofolic acid (5-Methyl THF) is the main circulating form of folic acid in the body and is involved in a variety of biochemical reactions. 5-Methyltetrahydrofolic acid regulates cardiovascular function by increasing the production of endothelin-1 (ET-1) in low-density lipoprotein-treated endothelial cells and can be used in the study of cardiovascular diseases [1] .
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10
10 Cited Publications
Cat. No.: HY-P0202
CAS No.: 117399-94-7
Synonyms: ET-1 (swine, human)
Endothelin 1 (swine, human) (ET-1) is a synthetic peptide with the sequence of human and swine Endothelin 1, which is a potent endogenous vasoconstrictor. Endothelin 1 acts through two types of receptors ETA and ETB [1].
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10
10 Cited Publications
Cat. No.: HY-P0202A
CAS No.: 394693-38-0
Synonyms: ET-1 (swine, human) TFA
Target:  

Endothelin Receptor

Research Areas:  

Cardiovascular Disease

Endothelin 1 (swine, human) (ET-1) TFA is a synthetic peptide with the sequence of human and swine Endothelin 1, which is a potent endogenous vasoconstrictor. Endothelin 1 TFA acts through two types of receptors ETA and ETB [1].
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4
4 Cited Publications
Cat. No.: HY-P71446
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: EDN1; PPET1; endothelin 1; ARCND3; endothelin-1; HDLCQ7; ET1; QME; Preproendothelin-1
Species:  
Rat
Source:  
E. coli
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1
1 Cited Publications
Cat. No.: HY-P4159
CAS No.: 133972-52-8
Target:  

ERK

Research Areas:  

Cardiovascular Disease

Endothelin-1 (1-31) (Human) is a potent vasoconstrictor and hypertensive agent. Endothelin-1 (1-31) (Human) is derived from the selective hydrolysis of big ET-1 by chymase [1].
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1
1 Cited Publications
Cat. No.: HY-P4159A
Target:  

ERK

Research Areas:  

Cardiovascular Disease

Endothelin-1 (1-31) (Human) TFA is a potent vasoconstrictor and hypertensive agent. Endothelin-1 (1-31) (Human) TFA is derived from the selective hydrolysis of big ET-1 by chymase [1].
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1
1 Cited Publications
Cat. No.: HY-P700460
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: EDN1; PPET1; endothelin 1; ARCND3; endothelin-1; HDLCQ7; ET1; QME; Preproendothelin-1
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P2538
CAS No.: 120796-97-6
Target:  

Vasopressin Receptor

Research Areas:  

Cardiovascular Disease

Big Endothelin-1 (1-38), human is the precursor of endothelin-1. Endothelin-1 (ET-1) is a potent vasopressor peptide [1].
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Cat. No.: HY-P4641
CAS No.: 6686-02-8
Synonyms: Trp-Phe
H-Trp-Phe-OH (Trp-Phe) is an ACE inhibitor and endothelial function regulator, with an ACE IC50 of 0.318 mg/mL. H-Trp-Phe-OH increases nitric oxide concentration, reduces endothelin-1 (ET-1) levels, and reverses norepinephrine-mediated endothelial cell dysfunction. H-Trp-Phe-OH exhibits antihypertensive activity. H-Trp-Phe-OH can be used in studies related to hypertension and atherosclerosis [1].
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Cat. No.: HY-113046S1
CAS No.: 212248-92-5
Synonyms: 5-Methyl THF-13C6; 5-MTHF-13C6
5-Methyltetrahydrofolic acid- 13C6 (5-Methyl THF- 13C6) is 13C labeled 5-Methyltetrahydrofolic acid. 5-Methyltetrahydrofolic acid (5-Methyl THF) is the main circulating form of folic acid in the body and is involved in a variety of biochemical reactions. 5-Methyltetrahydrofolic acid regulates cardiovascular function by increasing the production of endothelin-1 (ET-1) in low-density lipoprotein-treated endothelial cells and can be used in the study of cardiovascular diseases [1] .
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Cat. No.: HY-15538
CAS No.: 100981-43-9
Purity:  98.51%
Synonyms: FI3542
Ebrotidine (FI3542) is a competitive histamine H2 receptor (histamine H2 receptor) antagonist with gastric acid secretion inhibitory and gastric mucosal protective effects. Ebrotidine alleviates gastric mucosal injury and epithelial cell apoptosis induced by Indomethacin (HY-14397) and Helicobacter pylori LPS (HY-D1056), and accelerates chronic gastric ulcer healing by promoting rapid recovery of IL-4 and inhibiting TNF-α, endothelin-1 (ET-1) and NOS-2. Ebrotidine can be used in studies on gastric ulcer healing, NSAID-induced gastric mucosal injury, Helicobacter pylori-associated gastritis, and H2 receptor-mediated gastric mucosal protection mechanisms [1] .
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Cat. No.: HY-P3733
CAS No.: 124932-61-2
Target:  

Endothelin Receptor

Research Areas:  

Cardiovascular Disease

Big Endothelin-1 (22-38), human is derived from human, is the 22-38 fragment of Big Endothelin-1 (ET-1) (1-38). Big ET-1 (1-38) is a propeptide of ET-1, which has potent and long-lasting vasoconstrictor effects, equips a specific enzymatic cleavage of the 38 amino acid chain to form ET-1 (1-21) and the C-terminal fragment Big ET-1 (22-38) [1].
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Cat. No.: HY-19890
CAS No.: 14748-94-8
Synonyms: Aminaftone; Aminaphthone
Target:  

Endothelin Receptor

Aminaftone, a derivative of 4-aminobenzoic acid, downregulates endothelin-1 (ET-1) production in vitro by interfering with the transcription of the pre-pro-ET-1 gene.
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Cat. No.: HY-133829
CAS No.: 75176-37-3
Zofenoprilat is an angiotensin-converting enzyme (ACE) inhibitor with an IC50 of 1.7 nM. Zofenoprilat exerts cardioprotective and renoprotective effects by inhibiting angiotensin II expression and lowering blood pressure. Zofenoprilat promotes NO production and reduces endothelin-1 (ET-1) expression. Zofenoprilat decreases TNFα-induced ROS production and protects vascular endothelial function. Zofenoprilat regulates oxidative stress-related molecules and possesses antioxidant activity. Zofenoprilat can be used in studies related to hypertension and congestive heart failure [1] .
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Cat. No.: HY-15402
CAS No.: 210891-04-6
Synonyms: BMS 207940
Target:  

Endothelin Receptor

Research Areas:  

Cardiovascular Disease

Edonentan (BMS 207940) is an orally active, highly selective endothelin A receptor (ETA receptor) antagonist with a Ki value of 0.01 nM against human targets. Edonentan blocks the pressor response induced by Big Endothelin-1 in conscious normotensive rats and the pressor response induced by ET-1 in conscious normotensive cynomolgus monkeys. Edonentan can be used in research related to cardiovascular diseases [1].
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Cat. No.: HY-P4159B
Target:  

ERK

Research Areas:  

Cardiovascular Disease

Endothelin-1 (1-31) (Human) acetate is a potent vasoconstrictor and hypertensive agent. Endothelin-1 (1-31) (Human) acetate is derived from the selective hydrolysis of big ET-1 by chymase [1].
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Cat. No.: HY-10383
CAS No.: 198279-45-7
J-104132 (L-753037) is a potent, orally active, selective and competitive ETA/ETB receptor antagonist with Ki of 0.034 nM for ETA and 0.104 nM for ETB receptors. J-104132 inhibits Endothelin-1 (ET-1) (HY-P71446)-induced signaling and vascular contractions in vitro. J-104132 alleviates hypertension, vascular remodeling, and diabetic endothelial dysfunction in vivo by dual ETA/ETB blockade. J-104132 can be used for research on diabetic vascular complications [1][3].
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Cat. No.: HY-15402D
CAS No.: 264609-13-4
Synonyms: BMS 207940 hydrate
Target:  

Endothelin Receptor

Research Areas:  

Cardiovascular Disease

Edonentan hydrate (BMS 207940 hydrate) is an orally active, highly selective endothelin A receptor (ETA receptor) antagonist with a Ki value of 0.01 nM against human targets. Edonentan hydrate blocks the pressor response induced by Big Endothelin-1 in conscious normotensive rats and the pressor response induced by ET-1 in conscious normotensive cynomolgus monkeys. Edonentan hydrate can be used in research related to cardiovascular diseases [1].
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Cat. No.: HY-P2539
CAS No.: 120796-99-8
Target:  

Vasopressin Receptor

Research Areas:  

Cardiovascular Disease

Big Endothelin-1 (1-39), porcine is the precursor of endothelin-1. Endothelin-1 (ET-1) is a potent vasopressor peptide. Big Endothelin-1 (1-39), porcine has similar pressor effects in vivo [1].
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Cat. No.: HY-N5170
CAS No.: 156223-06-2
Aselacin A targets endothelin-1 receptor (ET-1 receptor), inhibits the the binding of ET-1 to ETA receptor and ETB receptor. Aselacin A inhibits the ET-1 binding to bovine atrial membrane and porcine cerebral membrane with IC50 of 22 μg/mL and 20 μg/mL. Aselacin A can be used for research of cardiovascular diseases [1].
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