64 Results for "

AT1 receptor antagonist

" in MedChemExpress (MCE) Product Catalog:
Products (64)

64 Results for "AT1 receptor antagonist" in MCE Product Catalog:

60
60 Publications Verification
Cat. No.: HY-17512
CAS No.: 114798-26-4
Synonyms: DuP-753
Losartan is an angiotensin II receptor antagonist, competing with the binding of angiotensin II to AT1 receptors with IC50 of 20 nM.
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60
60 Publications Verification
Cat. No.: HY-17512A
CAS No.: 124750-99-8
Synonyms: DuP-753 potassium
Losartan potassium (DuP-753 potassium) is an angiotensin II receptor type 1 (AT1) antagonist, competing with the binding of angiotensin II to AT1 with an IC50 of 20 nM.
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17
17 Cited Publications
Cat. No.: HY-13955
CAS No.: 144701-48-4
Purity:  99.79%
Synonyms: BIBR 277
Telmisartan is a potent, long lasting antagonist of angiotensin II type 1 receptor (AT1), selectively inhibiting the binding of 125I-AngII to AT1 receptors with IC50 of 9.2 nM.
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6
6 Cited Publications
Cat. No.: HY-14914
CAS No.: 147403-03-0
Purity:  99.68%
Synonyms: TAK-536
Azilsartan (TAK-536) is an orally active, potent, selective and specific angiotensin II type 1 receptor (AT1) antagonist. Azilsartan induces ROS formation and apoptosis in HepG2 cells. Azilsartan shows neuroprotective and anticancer activity. Azilsartan can be used for hypertension and stroke research .
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5
5 Cited Publications
Cat. No.: HY-B0780
CAS No.: 247257-48-3
Synonyms: BR-A-657
Fimasartan (BRA-657) is an orally effective angiotensin receptor AT1 non-peptide antagonist. Fimasartan has antihypertensive effects. Fimasartan improves neuroinflammation and brain injury mediated by NLRP3 inflammatome after intracerebral hemorrhage, and has neuroprotective effect. Fimasartan inhibits the expression of inducible nitric oxide synthase through the inactivation of NF-κB and activator protein-1 .
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1
1 Cited Publications
Cat. No.: HY-102093
CAS No.: 146709-78-6
Purity:  99.88%
ZD 7155 hydrochloride is an angiotensin II receptor type 1 (AT1 receptor) antagonist.
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Cat. No.: HY-12765
CAS No.: 124750-92-1
Purity:  98.95%
Synonyms: E-3174; EXP-3174
Losartan Carboxylic Acid (E-3174), an active carboxylic acid metabolite of Losartan, is an angiotensin II receptor type 1 (AT1) antagonist. The Ki values are 0.97, 0.57, 0.67 nM for rat AT1B/AT1A and human AT1, respectively. Losartan Carboxylic Acid blocks the angiotensin II-induced responses in vascular smoothmuscle cells (VSMC). Losartan Carboxylic Acid elevates plasma renin activities and reduces mean arterial pressure .
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Cat. No.: HY-17512AR
CAS No.: 124750-99-8
Synonyms: DuP-753 potassium (Standard)
Losartan (potassium) (Standard) is the analytical standard of Losartan (potassium). This product is intended for research and analytical applications. Losartan potassium (DuP-753 potassium) is an angiotensin II receptor type 1 (AT1) antagonist, competing with the binding of angiotensin II to AT1 with an IC50 of 20 nM.
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Cat. No.: HY-17512S
CAS No.: 1030937-27-9
Synonyms: DuP-753 d4
Losartan-d4 is the deuterium labeled Losartan. Losartan is an angiotensin II receptor antagonist, competing with the binding of angiotensin II to AT1 receptors with IC50 of 20 nM.
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Cat. No.: HY-12765S
CAS No.: 1246820-62-1
Purity:  98.17%
Synonyms: E-3174 d4; EXP-3174 d4
Losartan-d4 carboxylic acid (E-3174-d4) is the deuterium labeled Losartan Carboxylic Acid (HY-12765). Losartan Carboxylic Acid (E-3174), an active carboxylic acid metabolite of Losartan, is an angiotensin II receptor type 1 (AT1) antagonist. The Ki values are 0.97, 0.57, 0.67 nM for rat AT1B/AT1A and human AT1, respectively. Losartan Carboxylic Acid blocks the angiotensin II-induced responses in vascular smoothmuscle cells (VSMC). Losartan Carboxylic Acid elevates plasma renin activities and reduces mean arterial pressure.
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Cat. No.: HY-B0202S1
Irbesartan-d6 is the deuterium labeled Irbesartan. Irbesartan is a highly potent and specific angiotensin II type 1 (AT1) receptor antagonist with IC50 of 1.3 nM.
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Cat. No.: HY-13955S2
CAS No.: 1261396-33-1
Synonyms: BIBR 277-13C,d3
Telmisartan- 13C,d3 is the 13C- and deuterium labeled Telmisartan. Telmisartan is a potent, long lasting antagonist of angiotensin II type 1 receptor (AT1), selectively inhibiting the binding of 125I-AngII to AT1 receptors with IC50 of 9.2 nM.
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Cat. No.: HY-19732
CAS No.: 133085-33-3
Target:  

Angiotensin Receptor

Research Areas:  

Cardiovascular Disease

BIBS 39 is a non-peptide angiotensin II receptor antagonist with antihypertensive activity, with higher affinity for the AT1 receptor than for the AT2 receptor. BIBS 39 competitively blocks AT1-mediated vasoconstriction and pressor responses, and effectively inhibits the activity of the renin-angiotensin-aldosterone system. BIBS 39 reduces diastolic blood pressure and induces mild, transient reflex tachycardia, with no off-target functional activity on the norepinephrine, K +/Cl or vasopressin pathways. BIBS 39 can be used in research related to hypertension and renal hypertension [1][2 ][3].
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Cat. No.: HY-19165
CAS No.: 150438-02-1
Target:  

Angiotensin Receptor

Research Areas:  

Cardiovascular Disease

CI-996 is a potent, selective, orally active angiotensin II (Ang II) type 1 (AT1) receptor antagonist. In rat liver membranes CI-996 displaces specifically bind [ 125I]Ang II with an IC50 of 0.8 nM. CI-996 has blood pressure-lowering activity .
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Cat. No.: HY-13955S
CAS No.: 1189889-44-8
Purity:  99.77%
Telmisartan-d3 is the deuterium labeled Telmisartan. Telmisartan is a potent, long lasting antagonist of angiotensin II type 1 receptor (AT1), selectively inhibiting the binding of 125I-AngII to AT1 receptors with IC50 of 9.2 nM .
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Cat. No.: HY-13955S3
CAS No.: 1794754-60-1
Synonyms: BIBR 277-d7
Telmisartan-d7 (BIBR 277-d7) is a deuterium labeled Telmisartan (HY-13955). Telmisartan is a potent, long lasting antagonist of angiotensin II type 1 receptor (AT1), selectively inhibiting the binding of 125I-AngII to AT1 receptors with IC50 of 9.2 nM.
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Cat. No.: HY-17512S3
CAS No.: 1030936-22-1
Synonyms: DuP-753-d2
Losartan-d2 is the deuterium labeled Losartan . Losartan is an angiotensin II receptor antagonist, competing with the binding of angiotensin II to AT1 receptors with IC50 of 20 nM.
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Cat. No.: HY-101618
CAS No.: 169281-53-2
Target:  

Angiotensin Receptor

Research Areas:  

Cardiovascular Disease

L162389 is a potent antagonist of angiotensin AT1 receptor with Ki of 28 nM.
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Cat. No.: HY-A0229
CAS No.: 146623-69-0
Synonyms: GR 138950
Target:  

Angiotensin Receptor

Research Areas:  

Others

Saprisartan (GR 138950) is a selective, long-acting AT1 receptor antagonist with low receptor dissociation kinetics.
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Cat. No.: HY-105506
CAS No.: 114798-27-5
Target:  

Angiotensin Receptor

Research Areas:  

Cardiovascular Disease

EXP-7711 is a non peptide angiotensin II (Ang II) AT1 receptor antagonist. EXP-7711’s affinity for wild-type AT1 receptor (Ki =180 nM) is lower than peptide antagonists, but higher than losartan (Ki = 12 nM). EXP-7711 can be used for research on cardiovascular conditions .
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