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CAS No 100324-81-0 , 1H-Purine-2,6-dione,3,7-dihydro-1-[(5R)-5-hydroxyhexyl]-3,7-dimethyl- Search by region : China

  • Name: 1H-Purine-2,6-dione,3,7-dihydro-1-[(5R)-5-hydroxyhexyl]-3,7-dimethyl-
  • Synonyms: 1H-Purine-2,6-dione,3,7-dihydro-1-[(5R)-5-hydroxyhexyl]-3,7-dimethyl-; ProTec; CT 1501R;Lisophylline;1H-Purine-2,6-dione,3,7-dihydro-1-(5-hydroxyhexyl)-3,7-dimethyl-, (R)-; Lisofylline;
  • CAS Registry Number:
  • Flash Point: 263°C
  • Boiling Point: 511.2°C at 760 mmHg
  • Density: 1.32g/cm3
  • Refractive index: 1.62
  • Flash Point: 263°C
  • Molecular Weight: 0
  • InChI: InChI=1/C13H20N4O3/c1-9(18)6-4-5-7-17-12(19)10-11(14-8-15(10)2)16(3)13(17)20/h8-9,18H,4-7H2,1-3H3/t9-/m1/s1
  • Molecular Formula: C13H20 N4 O3
  • Molecular Structure:CAS No:100324-81-0 1H-Purine-2,6-dione,3,7-dihydro-1-[(5R)-5-hydroxyhexyl]-3,7-dimethyl-

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100324-81-0 LISOFYLLINE ( 3,7-DIHYDRO-1-[(5R)-5-HYDROXYHEXYL]-3,7-DIMETHYL-1H-PURINE-2,6-DIONE )

  • China Nanjing Chemlin Chemical Industry Co.,Ltd. [Manufacturer]
  • Tel: +86 25 8369-7070/ +86 138 51816776 (Mobile)
  • Fax: +86 25 8345-3275
  • Address: Rm.902 Longyin Plaza,
    No. 217 Zhongshan Rd.
    (N)Nanjing 210009,China null,nullChina
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References of 1H-Purine-2,6-dione,3,7-dihydro-1-[(5R)-5-hydroxyhexyl]-3,7-dimethyl-
Title: Lisofylline
CAS Registry Number: 100324-81-0
CAS Name: 3,7-Dihydro-1-[(5R)-5-hydroxyhexyl]-3,7-dimethyl-1H-purine-2,6-dione
Synonyms: 1-[(R)-5-hydroxyhexyl]theobromine; 1-(5R-hydroxyhexyl)-3,7-dimethylxanthine
Manufacturers' Codes: CT-1501R
Trademarks: ProTec (Cell Therapeutics)
Molecular Formula: C13H20N4O3
Molecular Weight: 280.32
Percent Composition: C 55.70%, H 7.19%, N 19.99%, O 17.12%
Literature References: Methylxanthine that inhibits production of phosphatidic acid during the inflammatory response. Identification as metabolite of pentoxifylline: H.-J. Hinze et al., Arzneim.-Forsch. 22, 1144 (1972). Enantioselective process: W. Aretz et al., DE 3942872; eidem, US 5310666 (1991, 1994 both to Hoechst). Asymmetric synthesis: J. P. Klein et al., WO 9531450 (1995 to Cell Therapeutics). Study of mechanism of action in septic shock: G. C. Rice et al., Proc. Natl. Acad. Sci. USA 91, 3857 (1994). Enhancement of hematopoietic recovery following 5-fluorouracil treatment in mice: E. Clarke et al., Cancer Res. 56, 105 (1996).
Properties: mp 110°. [a]D20 -5.6° (c = 6.7 in ethanol).
Melting point: mp 110°
Optical Rotation: [a]D20 -5.6° (c = 6.7 in ethanol)
Therap-Cat: Immunomodulator.
Keywords: Immunomodulator.