1957
DOI: 10.1021/ja01571a093
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S-(DICHLOROVINYL)-L-CYSTEINE: AN AGENT CAUSING FATAL APLASTIC ANEMIA IN CALVES1

Abstract: and ionic strength 0.02, w = 0.065 in the native state and w = 0.023 in the expanded state. These values of w require that the configurational change, at this temperature and ionic strength, at pH 3.5, should be accompanied by the binding of 29 protons per 67,000 g. If allowance is made for the fact that the radius of the expanded form is probably larger at ionic strength 0.02 than at ionic strength 0.04 (cf. serum albumin5), then the calculated proton uptake is increased to about 34. It thus appears that most… Show more

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Cited by 71 publications
(13 citation statements)
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“…Several 6-(substituted)-purities have been found to possess activity in many different biological systems; for example, they promote cell division in tobacco callus tissue,1 inhibit hydra tentacle regeneration,2 increase the rate of lettuce seed germination,3•4 stimulate moss bud formation,6 augment the growth inhibition of 2,4-diamino-6,7diphenylpteridine upon Lactobacillus arabinosus, 6 and recently have been observed to act synergistically with gibberellin in promoting seed germination.7 While the group substituted in the 6-position may be modified considerably with retention of biological activity, other changes in the purine nucleus have resulted in compounds which are inactive in most of these test systems. 8 In the present investigation, a number of the more effective 6-(substituted)-purine analogs were modified by introducing an amino group in the 2position.…”
mentioning
confidence: 99%
“…Several 6-(substituted)-purities have been found to possess activity in many different biological systems; for example, they promote cell division in tobacco callus tissue,1 inhibit hydra tentacle regeneration,2 increase the rate of lettuce seed germination,3•4 stimulate moss bud formation,6 augment the growth inhibition of 2,4-diamino-6,7diphenylpteridine upon Lactobacillus arabinosus, 6 and recently have been observed to act synergistically with gibberellin in promoting seed germination.7 While the group substituted in the 6-position may be modified considerably with retention of biological activity, other changes in the purine nucleus have resulted in compounds which are inactive in most of these test systems. 8 In the present investigation, a number of the more effective 6-(substituted)-purine analogs were modified by introducing an amino group in the 2position.…”
mentioning
confidence: 99%
“…Mice were mated overnight; the 19th day from start of pregnancy (obser-vation of vaginal plug=day 0) coincided with the first day after birth (approximately 6-12 hr post partum). (I4C-DCVC) and unlabelled DCVC were synthesized according to McKinney et al (1957) and purified on HPLC (Lichrosorb C,,, 3.8 x 300 mm; methanol-water 3:7 by vol. ; 1 ml/min.…”
Section: Methodsmentioning
confidence: 99%
“…of concentrate from 10.8 kg. of fraction I; yield of nitrogen, 64.9%; nitrogen content, 11.5%; total solids, 50.5%; and ash, 12.4%. Ratio of total nitrogen to amino nitrogen wras 3.59 to 1. Fractions N-l and N-2.…”
Section: Preparation Of Fractionsmentioning
confidence: 98%