熔点	120-121 ºC (ethanol )**
密度	1.156±0.06 g/cm3 (20 º

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来源	SDS样本
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New properties of chymotrypsin modified by fixation with a hydrophobic molecule: hexanal.M H Remy et al.Annals of the New York Academy of Sciences, 434, 343-346 (1984-01-01) Determination of the intrinsic Michaelis constant of immobilized alpha-chymotrypsin.S Blais et al.The Journal of biological chemistry, 268(25), 18637-18639 (1993-09-05) [Kinetic regularities of S2'-stimulation of alpha-chymotrypsin].S V Verevka Ukrainskii biokhimicheskii zhurnal (1978), 68(3), 36-41 (1996-05-01) Kinetics of N-glutaryl-L-phenylalanine p-nitroanilide hydrolysis catalyzed by alpha-chymotrypsin in aqueous solutions of alkyltrimethylammonium bromides.Elsa Abuin et al.Journal of colloid and interface science, 308(2), 573-576 (2007-01-26) Effect of human serum albumin on the kinetics of N-glutaryl-L-phenylalanine p-nitroanilide hydrolysis catalyzed by α-chymotrypsin.Elsa Abuin et al.The protein journal, 30(2), 143-147 (2011-02-22) Kinetics of N-glutaryl-L-phenylalanine p-nitroanilide hydrolysis catalyzed by alpha-chymotrypsin in aqueous solutions of dodecyltrimethylammonium bromide.Elsa Abuin et al.Journal of colloid and interface science, 283(2), 539-543 (2005-02-22) Occurrence and identity of proteolytic bacteria in adult periodontitis.D Grenier et al.Journal of periodontal research, 29(5), 365-370 (1994-09-01) Cell-permeable GPNA with appropriate backbone stereochemistry and spacing binds sequence-specifically to RNA.Anca Dragulescu-Andrasi et al.Chemical communications (Cambridge, England), (2)(2), 244-246 (2005-02-23) Immobilization of enzymes on a microchannel surface through cross-linking polymerization.Takeshi Honda et al.Chemical communications (Cambridge, England), (40)(40), 5062-5064 (2005-10-13) Clindamycin binding to ribosomes revisited: foot printing and computational detection of two binding sites within the peptidyl transferase center.O N Kostopoulou et al.Die Pharmazie, 68(7), 616-621 (2013-08-09) Novel 3-O-carbamoyl erythromycin A derivatives (carbamolides) with activity against resistant staphylococcal and streptococcal isolates.Thomas V Magee et al.Bioorganic & medicinal chemistry letters, 23(6), 1727-1731 (2013-02-19)

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