7 Results for "

Indoramin

" in MedChemExpress (MCE) Product Catalog:
Products (7)

7 Results for "Indoramin" in MCE Product Catalog:

Cat. No.: HY-12760
CAS No.: 26844-12-2
Purity:  99.80%
Synonyms: Indoramine; Wy 21901
Target:  

Adrenergic Receptor

Indoramin is an orally active antihypertensive agent. Indoramin is also selective for the α1A-adrenoceptor .
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1 Cited Publications
Cat. No.: HY-111208
CAS No.: 883098-58-6
Purity:  99.71%
Target:  

Phospholipase

Research Areas:  

Cancer

CCT129957 is an indole derivative and a potent phospholipase C-γ (PLC-γ) inhibitor with an IC50 of ~3 μM and a GC50 of 15 μM. CCT129957 inhibits Ca 2+ release in squamous carcinoma cells at ~15 μM .
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Cat. No.: HY-W009027
CAS No.: 38821-52-2
Synonyms: Indoramine hydrochloride; Wy 21901 hydrochloride
Target:  

Adrenergic Receptor

Research Areas:  

Cardiovascular Disease Others

Indoramin (hydrochloride) is a new hypotensive agent. Indoramin (hydrochloride) is also selective for the α1A-adrenoceptor .
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Cat. No.: HY-12760R
CAS No.: 26844-12-2
Synonyms: Indoramine (Standard); Wy 21901 (Standard)
Indoramin (Standard) is the analytical standard of Indoramin. This product is intended for research and analytical applications. Indoramin is an orally active antihypertensive agent. Indoramin is also selective for the α1A-adrenoceptor .
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Cat. No.: HY-12760S
CAS No.: 57165-41-0
Synonyms: Indoramine d5; Wy-21901 d5
Indoramin-d5 is deuterium labeled Indoramin, which is a piperidine antiadrenergic agent.
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Cat. No.: HY-111208R
CAS No.: 883098-58-6
Research Areas:  

Cancer

CCT129957 (Standard) is the analytical standard of CCT129957 (HY-111208). This product is intended for research and analytical applications. CCT129957 is an indole derivative and a potent phospholipase C-γ (PLC-γ) inhibitor with an IC50 of ~3 μM and a GC50 of 15 μM. CCT129957 inhibits Ca2+ release in squamous carcinoma cells at ~15 μM .
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Cat. No.: HY-119854
CAS No.: 89303-63-9
Synonyms: AY-28228
Atiprosine (AY-28228) is an orally effective selective α1-adrenergic receptor antagonist with a pA2 value of 8.11. Atiprosine exhibits antagonistic activity against α2-adrenergic receptors (α1-adrenergic receptor), 5-HT₂ receptors (5-HT₂ receptor), and H₁ receptors (H₁ receptor). The pA2 values for these receptors are 6.04, 6.87, and 7.32 respectively. Atiprosine has antihypertensive and hypotensive effects in rats, dogs, and monkeys. It can be used for research on cardiovascular and mental disorders.
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