26 Results for "

endothelial NOS

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

26 Results for "endothelial NOS" in MCE Product Catalog:

29
29 Publications Verification
Referencia número: HY-18731
No. CAS: 214358-33-5
Target:  

NO Synthase Apoptosis

Áreas de investigación:  

Cardiovascular Disease Inflammation/Immunology Cancer

1400W dihydrochloride is the dihydrochloride form of 1400W (HY-18730). 1400W is a slow, tight binding, and highly selective inducible nitric-oxide synthase (iNOS) inhibitor, with a Kd value ≤ 7 nM. 1400W inhibits iNOS induction in microglial cells, and reduces generation of NO, thereby mitigating oxidative stress and neuronal cell apoptosis in the rat cerebral cortex, and improving the spatial memory dysfunction caused by acute hypobaric hypoxia-reoxygenation .
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29
29 Publications Verification
Referencia número: HY-18730
No. CAS: 180001-34-7
Synonyms: W1400
Target:  

NO Synthase Apoptosis

Áreas de investigación:  

Cardiovascular Disease Inflammation/Immunology Cancer

1400W is a slow, tight binding, and highly selective inducible nitric-oxide synthase (iNOS) inhibitor, with a Kd value ≤ 7 nM. 1400W inhibits iNOS induction in microglial cells, and reduces generation of NO, thereby mitigating oxidative stress and neuronal cell apoptosis in the rat cerebral cortex, and improving the spatial memory dysfunction caused by acute hypobaric hypoxia-reoxygenation .
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5
5 Cited Publications
Referencia número: HY-113216
No. CAS: 30315-93-6
Pureza:  ≥98.0%
Synonyms: NG,NG-Dimethylarginine
Asymmetric dimethylarginine is an endogenous inhibitor of nitric oxide synthase (NOS), and functions as a marker of endothelial dysfunction in a number of pathological states.
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2
2 Cited Publications
Referencia número: HY-100986
No. CAS: 159190-44-0
Pureza:  ≥97.0%
Target:  

NO Synthase

Áreas de investigación:  

Cardiovascular Disease

L-NIO dihydrochloride is a potent, non-selective and NADPH-dependent nitric oxide synthase (NOS) inhibitor, with Kis of 1.7, 3.9, 3.9 μM for neuronal (nNOS), endothelial (eNOS), and inducible (iNOS), respectively . L-NIO dihydrochloride induces a consistentfocal ischemic infarctin rats .
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2
2 Cited Publications
Referencia número: HY-12119
No. CAS: 210354-22-6
Pureza:  ≥98.0%
Target:  

NO Synthase

Áreas de investigación:  

Neurological Disease Inflammation/Immunology

GW274150 is a potent, selective, orally active and NADPH-dependent inhibitor of human inducible nitric oxide synthase (iNOS) (IC50=2.19 μM; Kd=40 nM) and rat iNOS (ED50=1.15 μM). GW274150 also displays less potency for both humans or rats endothelial NOS (eNOS) and neuronal NOS (nNOS). GW274150 exerts a protective role in an acute model of lung injury inflammation .
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2
2 Cited Publications
Referencia número: HY-12119A
No. CAS: 438542-15-5
Pureza:  99.85%
Target:  

NO Synthase

Áreas de investigación:  

Neurological Disease Inflammation/Immunology

GW274150 phosphate is a potent, selective, orally active and NADPH-dependent inhibitor of human inducible nitric oxide synthase (iNOS) (IC50=2.19 μM; Kd=40 nM) and rat iNOS (ED50=1.15 μM). GW274150 phosphate displays less potency for both humans or rats endothelial NOS (eNOS) and neuronal NOS (nNOS). GW274150 phosphate exerts a protective role in an acute model of lung injury inflammation .
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1
1 Cited Publications
Referencia número: HY-102062
No. CAS: 137361-05-8
Pureza:  98.62%
Synonyms: N-omega-Propyl-L-arginine
Target:  

NO Synthase

Áreas de investigación:  

Neurological Disease

Nω-Propyl-L-arginine (N-omega-Propyl-L-arginine) is a potent, competitive, and highly selective inhibitor of neuronal nitric oxide synthase (nNOS), with a Ki of 57 nM. Nω-Propyl-L-arginine displays a 149-fold selectivity for nNOS over endothelial NOS (eNOS) .
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1
1 Cited Publications
Referencia número: HY-102062A
No. CAS: 2321366-46-3
Pureza:  98.28%
Synonyms: N-omega-Propyl-L-arginine hydrochloride
Target:  

NO Synthase

Áreas de investigación:  

Neurological Disease

Nω-Propyl-L-arginine (N-omega-Propyl-L-arginine) hydrochloride is a potent, competitive, and highly selective inhibitor of neuronal nitric oxide synthase (nNOS), with a Ki of 57 nM. Nω-Propyl-L-arginine hydrochloride displays a 149-fold selectivity for nNOS over endothelial NOS (eNOS) .
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1
1 Cited Publications
Referencia número: HY-W022047
No. CAS: 945762-00-5
Target:  

NO Synthase

Áreas de investigación:  

Cardiovascular Disease Neurological Disease

nNOS-IN-1(Compound 14) is an inhibitor for nitric oxide synthases (NOS), that exhibits inhibitory activities against neuroal, inducible and endothelial NOS, with IC50s of 2.5, 5.7 and 13 μM, respectively .
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1
1 Cited Publications
Referencia número: HY-P81191
Synonyms: eNOS (phospho S1177); eNOS(phospho S1177); p-eNOS (phospho S1177); eNOS (Phospho-Ser1177); cNOS; Constitutive NOS; EC NOS; ecNOS; endothelial nitric oxidase synthase; endothelial nitric oxide synthase; endothelial nitric oxide synthase 3; endothelial NOS; Nitric oxide synthase 3 (endothelial cell); Nitric oxide synthase 3; Nitric oxide synthase 3 endothelial cell; Nitric oxide synthase endothelial; nitric oxide synthase, endothelial; NOS 3; NOS III; NOS type III; NOS3; NOSIII; NOS3_HUMAN.

Host:  

Rabbit

Application:  

WB, ELISA, IHC-P, IHC-F, FC, ICC/IF

Reactivity:  

Human, Mouse

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1
1 Cited Publications
Referencia número: HY-P80656
Synonyms: NOS3; Nitric oxide synthase; endothelial; Constitutive NOS; cNOS; EC-NOS; endothelial NOS; eNOS; NOS type III; NOSIII

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF, ELISA

Reactivity:  

Human, Mouse, Rat

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Referencia número: HY-135224
No. CAS: 157254-60-9
Synonyms: 1,4-PB-ITU dihydrobromide
Target:  

NO Synthase

Áreas de investigación:  

Cancer

1,4-PBIT (1,4-PB-ITU) dihydrobromide (compound 46) is a potent nitric oxide synthases (NOS) inhibitor, with Ki values of 7.6 nM, 360 nM, and 16 nM for the inducible (iNOS), endothelial (eNOS), and neuronal (nNOS) isozymes, respectively .
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Referencia número: HY-100986B
No. CAS: 36889-13-1
Target:  

NO Synthase

Áreas de investigación:  

Cardiovascular Disease

L-NIO is a potent, non-selective and NADPH-dependent nitric oxide synthase (NOS) inhibitor, with Kis of 1.7, 3.9, 3.9 μM for neuronal (nNOS), endothelial (eNOS), and inducible (iNOS), respectively . L-NIO induces a consistentfocal ischemic infarctin rats .
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Referencia número: HY-123823
No. CAS: 175033-36-0
Pureza:  98.57%
Synonyms: NCX 4016
Target:  

NO Synthase Apoptosis STAT

Áreas de investigación:  

Inflammation/Immunology Cancer

Nitroaspirin (NCX 4016) is an orally active inhibitor of ARG1 and NOS2. Nitroaspirin reduces ARG1 enzymatic activity via the STAT6-mediated signaling pathway, and feedback-inhibits the catalytic activity of NOS2 in a NO-releasing group-dependent manner. Nitroaspirin continuously releases intracellular NO, inducing redox-dependent loss of cell viability. Nitroaspirin also exerts anti-angiogenic effects by causing endothelial barrier dysfunction, and effectively inhibits the proliferation of Cisplatin (HY-17394)-resistant human ovarian cancer cells . Nitroaspirin can be used in research related to colon cancer, breast cancer and Cisplatin-resistant human ovarian cancer .
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Referencia número: HY-113216S
Synonyms: NG,NG-Dimethylarginine-d7 hydrochloride hydrate
Asymmetric dimethylarginine-d7 (hydrochloride hydrate) is the deuterium labeled Asymmetric dimethylarginine. Asymmetric dimethylarginine is an endogenous inhibitor of nitric oxide synthase (NOS), and functions as a marker of endothelial dysfunction in a num
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Referencia número: HY-170236
No. CAS: 2945955-27-9
Target:  

NO Synthase

Áreas de investigación:  

Neurological Disease

nNOS-IN-5 (Compound 9) is a potent human neuronal NOS (nNOS) inhibitor (Ki = 22 nM). nNOS-IN-5 exhibits excellent selectivity, with a 900-fold preference for human nNOS over human endothelial NOS (eNOS). nNOS-IN-5 can be used for neurodegenerative diseases study, such as Alzheimer's disease and Parkinson’s disease .
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Referencia número: HY-18731R
No. CAS: 214358-33-5
Target:  

NO Synthase Apoptosis

Áreas de investigación:  

Cardiovascular Disease Inflammation/Immunology Cancer

1400W (Dihydrochloride) (Standard) is the analytical standard of 1400W (Dihydrochloride). This product is intended for research and analytical applications. 1400W dihydrochloride is the dihydrochloride form of 1400W (HY-18730). 1400W is a slow, tight binding, and highly selective inducible nitric-oxide synthase (iNOS) inhibitor, with a Kd value ≤ 7 nM. 1400W inhibits iNOS induction in microglial cells, and reduces generation of NO, thereby mitigating oxidative stress and neuronal cell apoptosis in the rat cerebral cortex, and improving the spatial memory dysfunction caused by acute hypobaric hypoxia-reoxygenation .
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Referencia número: HY-101304
No. CAS: 4269-97-0
Pureza:  ≥98.0%
Synonyms: S-isopropyl ITU; IPTU
Target:  

NO Synthase

Áreas de investigación:  

Cardiovascular Disease Neurological Disease

S-Isopropylisothiourea hydrobromide (S-isopropyl ITU; IPTU) is a blood-brain barrier (BBB) penetrant NOS inhibitor with IC50 values of 0.66, 0.75 and 0.29 μM against mouse spinal cord, cerebellar, bovine aortic and porcine endothelial cell NOS. S-Isopropylisothiourea exhibits a significant blood pressure-raising effect without damaging the perfusion of vital organs and can also inhibit the late-phase pain response induced by formalin. S-Isopropylisothiourea hydrobromide is used in the researchs for hemorrhagic shock and pain response based on NOS .
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Referencia número: HY-12119B
No. CAS: 438542-17-7
Target:  

NO Synthase

Áreas de investigación:  

Neurological Disease Inflammation/Immunology

GW274150 (dihydrochloride) is a potent, selective, orally active and NADPH-dependent inhibitor of human inducible nitric oxide synthase (iNOS) (IC50=2.19 μM; Kd=40 nM) and rat iNOS (ED50=1.15 μM). GW274150 (dihydrochloride) displays less potency for both humans or rats endothelial NOS (eNOS) and neuronal NOS (nNOS). GW274150 (dihydrochloride) exerts a protective role in an acute model of lung injury inflammation .
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Referencia número: HY-P85301A
Synonyms: NOS3; Nitric oxide synthase; endothelial; Constitutive NOS; cNOS; EC-NOS; endothelial NOS; eNOS; NOS type III; NOSIII

Host:  

Mouse

Application:  

WB, IHC-P, IHC-F, IF-Tissue

Reactivity:  

Mouse, Rat

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