143375-60-4|Y 26611|Y 26611|-范德生物科技公司

Y 26611

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names：
Y 26611
CAS号：
143375-60-4
MDL Number：
MF(分子式)： C18H19F2N3O4 MW(分子量)： 379.3638
EINECS: Reaxys Number:
Pubchem ID: Brand:BIOFOUNT

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中文别名	Y 26611
英文别名	Y 26611; Y-26611; Y26611.
CAS号	143375-60-4
SMILES	c1c2c(c(c(c1F)N3CCOC(C3)CN)F)n(cc(c2=O)C(=O)O)C4CC4
Inchi	InChI=1S/C18H19F2N3O4/c19-13-5-11-15(14(20)16(13)22-3-4-27-10(6-21)7-22)23(9-1-2-9)8-12(17(11)24)18(25)26/h5,8-10H,1-4,6-7,21H2,(H,25,26)
InchiKey	MVKGRIHKSLEKTE-UHFFFAOYSA-N
分子式 Formula	C18H19F2N3O4
分子量 Molecular Weight	379.3638
闪点 FP
熔点 Melting point
沸点 Boiling point
Polarizability极化度
密度 Density
蒸汽压 Vapor Pressure
溶解度Solubility
性状	Solid powder
储藏条件 Storage conditions	Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).

产品说明	Y 26611(CAS:143375-60-4):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。
Introduction	Y 26611 is a biochemical.
Application1
Application2
Application3

警示图
危险性	Warning
危险性警示
安全声明
安全防护
备注

[1]Sakurai N, Sano M, Hirayama F, Kuroda T, Uemori S, Moriguchi A, Yamamoto K, Ikeda Y, Kawakita T. Synthesis and structure-activity relationships of 7-(2-aminoalkyl)morpholinoquinolones as anti-Helicobacter pylori agents. Bioorg Med Chem Lett. 1998 Aug 18;8(16):2185-90. Erratum in: Bioorg Med Chem Lett 1998 Oct 20;8(20):2937. PubMed PMID: 9873510.

[2]Akter U, Niwa M, Nose T, Kaida T, Matsuno H, Kozawa O, Uematsu T. Effects of several agents on UVB- and UVA plus systemic fluoroquinolone-induced erythema of guinea pig skin evaluated by reflectance colorimetry. Free Radic Biol Med. 1998 May;24(7-8):1113-9. PubMed PMID: 9626565.

[3] Wada K, Saniabadi AR, Umemura K, Nakano M, Ito T, Nakashima M. Direct measurement of superoxide-dependent chemiluminescence from rat skin following UV-dependent fluoroquinolone-induced dermatitis. Free Radic Biol Med. 1995 May;18(5):923-7. PubMed PMID: 7797102.

[4] Kubo S, Matsumoto T, Takahashi K, Haraoka M, Tanaka M, Sakumoto M, Sakamoto Y, Kumazawa J. Enhanced chemiluminescence response of polymorphonuclear leukocytes by new quinolone antimicrobials. Chemotherapy. 1994 Sep-Oct;40(5):333-6. PubMed PMID: 7956457.

[5] Wada K, Saniabadi AR, Umemura K, Takiguchi Y, Nakashima M. UV-dependent quinolone-induced human erythrocyte membrane lipid peroxidation: studies on the phototoxicity of Y-26611, a new quinolone derivative. Pharmacol Toxicol. 1994 Apr-May;74(4-5):240-3. PubMed PMID: 8090693.

6: Araki K, Kuroda T, Uemori S, Moriguchi A, Ikeda Y, Hirayama F, Yokoyama Y, Iwao E, Yakushiji T. Quinolone antimicrobial agents substituted with morpholines at the 7-position. Syntheses and structure-activity relationships. J Med Chem. 1993 May 14;36(10):1356-63. PubMed PMID: 8388467.7: Tomioka H, Sato K, Saito H. [Antimicrobial activity of new quinolones against Mycobacterium avium and Mycobacterium intracellulare determined by the dilution methods using 7H11 agar and Ogawa egg media]. Kekkaku. 1993 May;68(5):367-70. Japanese. PubMed PMID: 8331881.8: Tomioka H, Sato K, Saito H, Ikeda Y. [Antimycobacterial activity of a newly synthesized fluoroquinolone, Y-26611]. Kekkaku. 1992 Jul;67(7):515-20. Japanese. PubMed PMID: 1331603.

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