72 Results for "

ET-1

" in MedChemExpress (MCE) Product Catalog:
Products (72)

72 Results for "ET-1" in MCE Product Catalog:

15
15 Publications Verification
Cat. No.: HY-15894A
CAS No.: 173326-37-9
Purity:  98.66%
BQ-788 is a potent, selective ETB receptor antagonist with IC50 of 1.2 nM for inhibition of ET-1 binding to human Girardi heart cells, poorly inhibiting the binding to ETA receptors in human neuroblastoma cell line SK-N-MC cells with IC50 of 1300 nM [1].
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15
15 Publications Verification
Cat. No.: HY-15894
CAS No.: 156161-89-6
Purity:  99.33%
BQ-788 sodium salt is a potent and selective ETB receptor antagonist, inhibiting ET-1 binding to ETB receptors with an IC50 of 1.2 nM in human Girrardi heart cells [1].
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12
12 Cited Publications
Cat. No.: HY-B1100
CAS No.: 313-06-4
Estradiol cypionate is the 17β-cypionate ester of Estradiol, which inhibits ET-1 synthesis by acting on estrogen receptors [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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9
9 Cited Publications
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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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:  
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2
2 Cited Publications
Cat. No.: HY-N2575
CAS No.: 77029-83-5
Hypocrellin A is a PKC inhibitor that exerts antidiabetic activity by reversing the effects of high glucose on endothelin (ET-1) expression. Hypocrellin A is also a photosensitizer for photodynamic therapy (PDT) with anticancer, antibacterial and antiviral activities, especially against human immunodeficiency virus (HIV). In addition, Hypocrellin-A also possesses anti-Leishmania activity (IC50=0.27 μg/ml) [1] .
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2
2 Cited Publications
Cat. No.: HY-120295
CAS No.: 195529-54-5
Purity:  99.51%
A-192621, a chemical probe, is a potent, nonpeptide, orally active and selective endothelin B (ETB) receptor antagonist with an IC50 of 4.5 nM and a Ki of 8.8 nM. The selectivity of A-192621 is 636-fold higher than ETA (IC50 of 4280 nM and Ki of 5600 nM). A-192621 promotes apoptosis in PASMCs. A-192621 alos causes elevation of arterial blood pressure and an elevation in the plasma ET-1 level [1] .
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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-17352
CAS No.: 180384-56-9
Synonyms: Ro 61-1790; VML 588; AXV-034343
Target:  

Endothelin Receptor

Research Areas:  

Cardiovascular Disease

Clazosentan (Ro 61-1790) is a selective endothelin A (ETA) receptor antagonist. Clazosentan inhibits ET-1-mediated vasoconstriction. Clazosentan prevents cerebral vasospasm, vasospasm-related cerebral infarction [1] .
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1
1 Cited Publications
Cat. No.: HY-114367
CAS No.: 15674-58-5
Purity:  98.83%
Synonyms: Delphinidin 3-O-rutinoside chloride
Delphinidin 3-rutinoside chloride is an anthocyanin component. Delphinidin 3-rutinoside chloride is isolable from the fruits of blackcurrant Ribes nigrum L. Delphinidin 3-rutinoside chloride activates the ETB receptor and stimulates the NO/cGMP pathway. Delphinidin 3-rutinoside chloride increases cyclic guanosine monophosphate production and reduces the phosphorylation level of Myosin regulatory light chain. Delphinidin 3-rutinoside chloride stimulates GLP-1 secretion. It significantly induces relaxation of bovine ciliary muscle strips contracted by ET-1 and inhibits ET-1-induced contraction of bovine ciliary muscle strips. Delphinidin 3-rutinoside chloride is applicable to research related to type 2 diabetes [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-17352A
CAS No.: 503271-02-1
Synonyms: Ro 61-1790 disodium; VML 588 disodium; AXV-034343 disodium
Target:  

Endothelin Receptor

Research Areas:  

Cardiovascular Disease

Clazosentan disodium (Ro 61-1790) is a selective endothelin A (ETA) receptor antagonist. Clazosentan disodium inhibits ET-1-mediated vasoconstriction. Clazosentan disodium prevents cerebral vasospasm, vasospasm-related cerebral infarction [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:  
Source:  
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Cat. No.: HY-N7543
CAS No.: 64917-82-4
Schisantherin D is a lignan. Schisantherin D can be isolated from Kadsura interior. Schisantherin D downregulates the expression of ETBR and inhibits the secretion of ECM and ET-1. Schisantherin D alleviates EtOH + ET-1-induced hepatocyte cytotoxicity. Schisantherin D potently inhibits HIV replication in cells [1] .
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Cat. No.: HY-118060
CAS No.: 24587-37-9
Purity:  97.89%
Synonyms: N-Valyltryptophan; Val-Trp
Dipeptide 2 (N-Valyltryptophan) is an orally active, competitive angiotensin-converting enzyme (ACE) inhibitory peptide with an IC50 of 10.50 μM. Dipeptide 2 reduces intracellular Calcium ions. Dipeptide 2 significantly increases the content of NO, inhibits the production of ET-1, and induces the phosphorylation of eNOS. Dipeptide 2 decreases the systolic and diastolic blood pressure of spontaneously hypertensive rats [1].
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Cat. No.: HY-15195
CAS No.: 290815-26-8
Purity:  98.15%
Synonyms: Ro 67-0565; SPP-301
Target:  

Endothelin Receptor

Avosentan (Ro 67-0565; SPP-301) is an orally active endothelin (ETA) receptor antagonist. Avosentan can block the ETA receptor, thereby reducing vascular contraction and exerting a renal protective effect. Avosentan inhibits vascular contraction caused by ET-1 and alleviates the reduction in retinal and optic nerve head blood flow induced by it, lowering intraocular pressure in the glaucoma monkey model. Avosentan non-specifically blocks ETB receptors at high doses, inhibiting ETB-mediated diuresis and natriuresis, and may cause fluid retention. Avosentan can be used to reduce proteinuria with diabetic nephropathy, but induces significant fluid overload and congestive heart failure [1] .
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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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