化合物信息

02101997 

Hydrochloride
Slowly decomposes when moist.
Purity: 96% minimum

02152528 

Hydrochloride
ACS Reagent Grade
Purity: ≥96.0%

05213650 

MP Biomedicals Rare Chemical collection

H2391 

Biochem/physiol Actions
MAO 抑制剂;抑制血小板聚集。

379921 

Biochem/physiol Actions
MAO 抑制剂;抑制血小板聚集。
包装
5, 25 g in poly bottle
Application
Reactant for preparation of:
• Organosilane amines as potent inhibitors and structural probes of influenza A virus M2 proton channel1
• Lamellarin D analogues as inibitors of topoisomerase I and potential antitumor agents2
• Azapeptide tocolytic agents as inhibitors of prostaglandin F2α receptor for preventing preterm labor3
• Thiazolidinones spiro-fused to indolin-2-ones as potent and selective inhibitors of Mycobacterium tuberculosis protein tyrosine phosphatase B4
• Orally bioavailable quinoline-based antidiabetic dipeptidyl peptidase IV inhibitors targeting Lys5545
• Pyrimidine nucleoside derivatives with nitric oxide donors as antiviral agents6
• Benzyladenosine compounds targeting adenosine A2A receptor and adenosine transporter for neuroprotection7
• Naphthol derivatives as inhibitors of the vanilloid receptor TRPV1 with improved potency in rat cystometry models of urinary incontinence8

431362 

Biochem/physiol Actions
MAO 抑制剂;抑制血小板聚集。
Features and Benefits
符合 A.C.S. 的试剂规范。
包装
50, 250 g in poly bottle
Application
Reactant for preparation of:
• Organosilane amines as potent inhibitors and structural probes of influenza A virus M2 proton channel1
• Lamellarin D analogues as inibitors of topoisomerase I and potential antitumor agents2
• Azapeptide tocolytic agents as inhibitors of prostaglandin F2a receptor for preventing preterm labor3
• Thiazolidinones spiro-fused to indolin-2-ones as potent and selective inhibitors of Mycobacterium tuberculosis protein tyrosine phosphatase B4
• Orally bioavailable quinoline-based antidiabetic dipeptidyl peptidase IV inhibitors targeting Lys5545
• Pyrimidine nucleoside derivatives with nitric oxide donors as antiviral agents6
• Benzyladenosine compounds targeting adenosine A2A receptor and adenosine transporter for neuroprotection7
• Naphthol derivatives as inhibitors of the vanilloid receptor TRPV1 with improved potency in rat cystometry models of urinary incontinence8

55469 

Biochem/physiol Actions
MAO 抑制剂;抑制血小板聚集。

11514 

Biochem/physiol Actions
MAO 抑制剂;抑制血小板聚集。
法律信息
TraceSELECT 注册商标 Sigma-Aldrich Co. LLC

55459 

Biochem/physiol Actions
MAO 抑制剂;抑制血小板聚集。

255580 

Application
强还原剂。可将醛和酮转化为肟，将酰基氯转化为氧肟酸。可用作催化剂、溶胀剂和共聚反应抑制剂。
Biochem/physiol Actions
MAO 抑制剂;抑制血小板聚集。
包装
100, 500 g in poly bottle
5 g in glass bottle

159417 

Biochem/physiol Actions
MAO 抑制剂;抑制血小板聚集。
包装
100, 500 g in poly bottle
3 kg in poly drum
3kg 开口塑料桶包装；100g、500g 塑料瓶包装
法律信息
ReagentPlus 注册商标 Sigma-Aldrich Co. LLC

55460 

Biochem/physiol Actions
MAO 抑制剂;抑制血小板聚集。

13-2290 

Biochem/physiol Actions
MAO 抑制剂;抑制血小板聚集。

13-2291 

Biochem/physiol Actions
MAO 抑制剂;抑制血小板聚集。

13-2280 

Biochem/physiol Actions
MAO 抑制剂;抑制血小板聚集。