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Detail of "58626-38-3"

  • MSDS Download
  • CAS Number:
  • 58626-38-3
  • Name:
  • Benzoic acid,3-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)-, 2,5-dioxo-1-pyrrolidinyl ester

  • Superlist Name:
  • 3-Maleimidobenzoic acid N-hydroxysuccinimide ester
  • Molecular Structure:
  • Formula:
  • C15H10 N2 O6
  • Molecular Weight:
  • 314.2497
  • Synonyms:
  • 1H-Pyrrole-2,5-dione,1-[3-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]phenyl]- (9CI); MBS; MMBS;N-(3-Maleimidobenzoyloxy)succinamide; N-(m-Maleimidobenzoyloxy)succinamide;N-(m-Maleimidobenzoyloxy)succinimide; NSC 294786; m-Maleimidobenzoic acidN-hydroxysuccinimide ester; m-Maleimidobenzoyl N-hydroxysuccinimide ester;m-Maleimidobenzoyl-N-hydroxysuccinimide
  • EINECS:
  • 261-368-8
  • Density:
  • 1.59 g/cm3
  • Melting Point:
  • 175-177 °C(lit.)
  • Boiling Point:
  • 524.5 °C at 760 mmHg
  • Flash Point:
  • 271 °C
  • Appearance:
  • Crystalline
  • Hazard Symbols:
  • Risk Codes:
  • R36/37/38   
  • Safety:
  • 26-36 Details

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CAS No.58626-38-3 3-Maleimidobenzoic acid N-hydroxysuccinimide ester

3-Maleimidobenzoic acid N-hydroxysuccinimide ester

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CAS No.58626-38-3 3-Maleimidobenzoic acid N-hydroxysuccinimide ester

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CAS No.58626-38-3 3-Maleimidobenzoic acid N-hydroxysuccinimide ester

3-Maleimidobenzoic acid N-hydroxysuccinimide ester

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CAS No.58626-38-3 3-Maleimidobenzoic acid N-hydroxysuccinimide ester

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CAS No.58626-38-3 3-Maleimidobenzoic acid N-hydroxysuccinimide ester

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Reference

Enzyme immunoassay of the antibiotic viomycin
Enzyme immunoassay of the antibiotic viomycin. Fujitake, Takafumi; Kitagawa, Tsunehiro; Aikawa, Tadaomi (Fac. Pharm. Sci., Nagasaki Univ., Nagasaki, Japan). Rinsho Kagaku Shimpojumu, 16, 18-22 (Japanese) 1976. CODEN: RKASDA. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacodynamics) Viomycin (I) [32988-50-4] (6 .mu.mol) was treated with N-(m-maleimidobenzyloxy)succinimide (MBS) [58626-38-3] and .beta.-galactosidase [9031-11-2] to obtain a I-MBS-.beta.-galactosidase conjugate. The conjugate was treated with various concns. of antiserum to I in the presence or in the absence of I, and the enzyme activities of resulting ppts. were measured. The competitive binding test between the conjugate and I to the I-antiserum indicated that I is detected at concns. ranging between 100 pg to 4 ng.
Chemical methods for the modification of liposomes with proteins or antibodies
Chemical methods for the modification of liposomes with proteins or antibodies. Hashimoto, Yoshiyuki; Endoh, Hiroo; Sugawara, Minoru (Dep. Hyg. Chem., Tohoku Univ., Sendai, Japan). Liposome Technol., Volume 3, 41-9. Edited by: Gregoriadis, Gregory. CRC: Boca Raton, Fla. (English) 1984. CODEN: 52BBAJ. DOCUMENT TYPE: Conference CA Section: 63 (Pharmaceuticals) Section cross-reference(s): 6 Tolylene 2,4-diisocyanate (TDIC) [584-84-9], a crosslinking reagent binding 2 NH2 groups, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDCI) [1892-57-5], binding NH2 and CO2H groups, and m-maleimidobenzoyl-N-hydroxysuccinimide ester (MBS) [58626-38-3] crosslinking NH2 and SH groups, were used as coupling agents to prep. protein-or antibody-modified liposomes. TDIC was used to prepd. dansyl-bovine serum albumin-modified liposomes, EDCI for anti-SRBC IgG modified liposome, and MBS reactions with phospholipids. Assay of liposome-surface protein, targeting of antibody-modified liposomes to antigenic cells, and application of antibody-modified liposomes are discussed.
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