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Detail of "90-34-6"

  • CAS Number:
  • 90-34-6
  • Name:
  • 1,4-Pentanediamine,N4-(6-methoxy-8-quinolinyl)-

  • Superlist Name:
  • Primaquine
  • Molecular Structure:
  • Formula:
  • C15H21 N3 O
  • Molecular Weight:
  • 259.39
  • Synonyms:
  • Quinoline,8-[(4-amino-1-methylbutyl)amino]-6-methoxy- (6CI,8CI); (?à)-Primaquine;6-Methoxy-8-[4-amino-1-methylbutylamino]quinoline;8-(4-Amino-1-methylbutylamino)-6-methoxyquinoline; NSC 27296; Neo-Quipenyl;Primachin; Primaquin; Primaquine; SN 13272; WR 2975; dl-Primaquine
  • EINECS:
  • 201-987-2
  • Safety:
  • Poison by ingestion and intravenous routes. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx. Details

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CAS No.90-34-6 Primaquine

Assay:98%  Appearance:powder  Package:drum

Supplier:WU HAN ERELI Import and Export Co., Ltd [ China (Mainland)]

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CAS No.90-34-6 Primaquine

Supplier:ChemOrganic Limited [ China (Mainland)]

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1375Integral
1375

Tel:0571-28183299

Address:Room 608,Building B , Zhejiang University science park, #525 Xixi Road ,hangzhou,China.

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CAS No.90-34-6 Primaquine

Supplier:SHIJIAZHAUNG KUNLI CHEMICAL CO.LTD., [ China (Mainland)]

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1570Integral
1570

Tel:0311-85233798

Address:shijiazhuang

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CAS No.90-34-6 Primaquine

Supplier:Hangzhou Dayangchem Co., Ltd. [ China (Mainland)]

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ISO 3875Integral
3875

Tel:+86-571-88938639

Address:B/2601 Fuli Building, 328# WenEr Rd. Hangzhou City 310012 China

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CAS No.90-34-6 Primaquine

BP88

Supplier:ZHOU FANG PHARM CHEMICAL [ China (Mainland)]

620Integral
620

Tel:+86-134-8227-9455

Address:1230 Zhongshan Road, Shanghai, China.

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CAS No.90-34-6 Primaquine

Primaquine Phosphate???BP2002/USP29

Supplier:ChangZhou XiXiaLong International Co., Ltd [ China (Mainland)]

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500

Tel:+86-519-85120628

Address:Room 5002, Modern city,Huangshanlu, Xinbei district, Changzhou, China

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CAS No.90-34-6 Primaquine

Supplier:ecochem international chemical broker [ Denmark]

600Integral
600

Tel:+45 45 42 34 36

Address:ecochem international chemical broker

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Reference

In vitro metabolism of the antimalarial agent primaquine by mouse liver enzymes and identification of a methemoglobin-forming metabolite
In vitro metabolism of the antimalarial agent primaquine by mouse liver enzymes and identification of a methemoglobin-forming metabolite. Strother, A.; Allahyari, R.; Buchholz, J.; Fraser, I. M.; Tilton, B. E. (Sch. Med., Loma Linda Univ., Loma Linda, CA 92350, USA). Drug Metab. Dispos., 12(1), 35-44 (English) 1984. CODEN: DMDSAI. ISSN: 0090-9556. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacology) A metHb-forming metabolite of primaquine (I)(PQ) [90-34-6] was isolated and identified from a mouse liver microsomal system. Both O-dealkylationa nd hydroxylation of PQ to form a metabolite, 5,6-dihydroxy-8-(4-amino-1-methylbutylamino)quinoline [87321-06-0], which is highly active in forming metHb in both normal and glucose-6-phosphate dehydrogenase-deficient erythrocytes were obsd. The metabolite also actively decreases glutathione levels in glucose-6-phosphate dehydrogenase-deficient erythrocytes. The inhibitor SKF 525-A prevented metabolite formation, whereas iproniazid and CO did not inhibit metab. completely but may have resulted in formation of a different unidentified metabolite. This addnl. metabolite was identified indirectly via a blue compd. [89202-75-5] which results from extg.There are some commonly used reagents with their cas registry numbers 89202-75-5 and 90-34-6 in this article. the actual metabolite from the incubation mixt. with org. solvents under alk. conditions in the presence of light. The blue compd. was identified as a quinonimine in which the 8-amino side chain of PQ cyclizes to produce a 3 ring system. .
Effect of ascorbic acid on hemolysis induced by primaquine in vitro
Effect of ascorbic acid on hemolysis induced by primaquine in vitro. Grinberg, L. N.; Nguyen Kim Phong (Inst. 90-34-6 and 50-81-7 are also occured in this study. Med. Parazitol. Trop. Med., Moscow, USSR). Gematol. Transfuziol., 28(12), 50-2 (Russian) 1983. CODEN: GETRE8. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacology) Section cross-reference(s): 18 Ascorbic acid [50-81-7] (0.5-2.0 mM) inhibited primaquine [90-34-6] (3.0 mM)-induced accumulation of metHb and lysis of human erythrocytes during a 2-h incubation at 37°. The protective effect of ascorbate was greater than that of NaCHO2. NaCHO2 did not enhance the effect of ascorbate. .
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