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Detail of "14919-77-8"

  • CAS Number:
  • 14919-77-8
  • Name:
  • Benserazide hydrochloride

  • Molecular Structure:
  • Formula:
  • C10H15N3O5.HCl
  • Molecular Weight:
  • 293.74
  • Deleted CAS:
  • 14046-64-1|31796-68-6
  • Synonyms:
  • Serine,2-[(2,3,4-trihydroxyphenyl)methyl]- hydrazide,monohydrochloride;Ro 4-4602;Benserazide HCl;Serinehydrazide hydrochloride;Benserazide hydrochloride 98.5%;2'-(2,3,4-trihydroxybenzyl)-DL-serinohydrazide monohydrochloride;
  • EINECS:
  • 238-991-9
  • Melting Point:
  • 146 °C
  • Boiling Point:
  • 574.2 °C at 760 mmHg
  • Flash Point:
  • 301 °C
  • Appearance:
  • white crystalline solid
  • Hazard Symbols:
  • IrritantXi
  • Risk Codes:
  • 36/37/38
  • Safety:
  • 26-36 Details

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CAS No.14919-77-8 Benserazide hydrochlorideCompetitive Product

Molecular Formula C10H15N3O5.HCl Molecular Weight 293.71 CAS Registry Number 14919-77-8 EINECS 238-991-9 Quantity standard EP7 EDMF

Supplier:Wuhan Shiji Pharmaceutical Co., Ltd [ China (Mainland)]

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CAS No.14919-77-8 Benserazide hydrochlorideCompetitive Product

  Package:in tin

Name: Benserazide Hydrochloride Standard: EP

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CAS No.14919-77-8 Benserazide hydrochlorideCompetitive Product

Benserazide Hydrochloride EP5.0

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CAS No.14919-77-8 Benserazide hydrochlorideCompetitive Product

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CAS No.14919-77-8 Benserazide hydrochloride

(RS)-2-amino-3-hydroxy-2'(2,3,4-trihydroxhbenzyl)

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CAS No.14919-77-8 Benserazide hydrochloride

Assay:99%  Appearance:powder  Package:25kg/drum

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CAS No.14919-77-8 Benserazide hydrochloride

Assay:98%  Appearance:White or alm...

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CAS No.14919-77-8 Benserazide hydrochloride

Assay:98%

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CAS No.14919-77-8 Benserazide hydrochloride

Benserazide Hydrochloride ---We supply this product in very competitive price.

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CAS No.14919-77-8 Benserazide hydrochloride

Assay:99%  Appearance:white crysta...  Package:1kg/foil bagStorage:5kg  Transportation:by sea/air/e...  Application:pharmaceutic...

product Name: Benserazide hydrochloride Molecular Formula: C9H14ClN3O5 Molecular Weight: 279.67756 Melting point :146℃ CAS No:14046-64-1;14919-77-8

Min. Order:1Kilogram

Supplier:Hubei Yuancheng Pharmaceutical Co.,Ltd [ China (Mainland)]

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CAS No.14919-77-8 Benserazide hydrochloride

Benserazide Hydrochloride (HCL) Molecular Formula:C10H15N3O5.HCl Molecular Weight:293.71 CAS NO:14919-77-8 EINECS:238-991-9 Quality standard:EP/BP Assay(HPLC):98.5% min Appearance:White or similar to white crystalinel powder, freely soluble in water, very slightl

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Benserazide HCL

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CAS No.14919-77-8 Benserazide hydrochloride

Appearance]White or similar to white crystal powder [Identification]Infra-red IR [Specific optical rotation ]-0.05°-+0.05° [Drying loss]≤1.0%

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CAS No.14919-77-8 Benserazide hydrochloride

Benserazide hydrochloride Molecular formula:C10H15N3O5.HCL CAS No:14919-77-8 Property:white or similar to white crystal powder Assay: Min98.5% Quality standard:EP5.0

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CAS No.14919-77-8 Benserazide hydrochloride

Benserazide hydrochloride(Serazide) is a peripherally-acting aromatic L-amino acid decarboxylase (AAAD) or DOPA decarboxylase inhibitor.

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CAS No.14919-77-8 Benserazide hydrochloride

benserazide hydrochloride

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Supplier:Hubei Nanxing Pharmaceutical Co.,Ltd. [ China (Mainland)]

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Supplier:Hubei Hengluyuang Technology Co.,Ltd [ China (Mainland)]

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Supplier:RA Chem Pharma Limited [ India]

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Supplier:Clearsynth Labs (P) Ltd. [ India]

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CAS No.14919-77-8 Benserazide hydrochloride

Benserazide hydrochloride

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Reference

Pharmacological studies on L-DOPA and DOPA decarboxylase inhibitors
Pharmacological studies on L-DOPA and DOPA decarboxylase inhibitors. Effect on the central nervous system with a combination of L-DOPA and benserazide hydrochloride. Takahashi, Noriyuki (Dep. Pharmacol., Tokyo Med. Coll., Tokyo, Japan). Tokyo Ika Daigaku Zasshi, 35(4), 715-30 (Japanese) 1977. CODEN: TIDZAH. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacodynamics) L-Dopa [59-92-7] and a dopa decarboxylase inhibitor, benserazide-HCl (I-HCl) [14919-77-8], in combination (500 and 200 mg/kg, resp.,) administered orally to monkeys induced abnormal behavior, although the administration of each compd. alone was without effect. The combination of dopa and I (100 and 25 mg/kg, orally) given to rats decreased body temp. and 200 and 50 mg/kg, resp., markedly increased dopamine [51-61-6] level in the brain, suggesting that the dose of dopa for the treatment of parkinsonism may be reduced if it is combined with I.
Pineal aryl acylamidase: effects of melatonin, serotonin-related compounds, B-carbolines, RO4-4602 and antidepressants
Pineal aryl acylamidase: effects of melatonin, serotonin-related compounds, B-carbolines, RO4-4602 and antidepressants. Hsu, Louise L. (Dep. Psychiatry Behav. Sci., Univ. Texas, Galveston, TX 77550, USA). 14919-77-8 and 51-41-2 are also occured in this study. Res. Commun. Chem. Pathol. Pharmacol., 43(2), 223-34 (English) 1984. CODEN: RCOCB8. ISSN: 0034-5164. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacology) Section cross-reference(s): 2, 7 The pineal aryl acylamidase (AAA) [9025-18-7] activity has been demonstrated and characterized for the first time using ONAc as a substrate. The pineal AAA activity in the presence of 0.05% Triton X-100 was linear with protein concn. up to 1 mg and with incubation time up to 1 h. Both the rat and bovine pineal showed a pH optimum at 5.0. The in vitro and in vivo effects of several classes of drugs on the pineal AAA activity were examd. At 0.1 mM, 5-HT creatinine sulfate [971-74-4], N-acetyl-5HT [1210-83-9], melatonin [73-31-4], d-LSD [50-37-3], l-LSD [2126-78-5], methiothepin [20229-30-5], dopamine [51-61-6], chlorimipramine [303-49-1], imipramine [50-49-7], pargyline [555-57-7], tetrahydro-b-carboline (THBC) [16502-01-5], and harmaline [304-21-2] significantly inhibited the rat pineal AAA activity by 19-51%. N-acetyl-5-HT was the most potent in vitro inhibitor. However, at the same concn., norepinephrine [51-41-2], 6-MeO-harman [3589-72-8] and eserine [57-47-6] did not show any effect on the enzyme activity. Lineweaver-Burk plots indicated a competitive type of in vitro inhibition of the pineal AAA activity by melatonin. Acute s.c. injection of low doses (25-50 mg/kg) THBC, harmaline, desipramine [50-47-5], and protryptyline [438-60-8] markedly inhibited the rat pineal AAA activity, but at higher doses (75-700 mg/kg) the inhibition was reduced. On the contrary, RO4-4602 [14919-77-8] (200-800 mg/kg) enhanced 1.5-2.3-fold the enzyme activity, inversely proportional to the doses given. In view of the differential effects of these drugs on brain AAA and pineal AAA, it seems unlikely that they would be the same enzyme. .
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