ライフサイエンスコーパス: mercaptan

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1 an and cis-fused product from Z-homoallyllic mercaptan.

2 selectively rupture into a set of monomeric mercaptans.

3 gen sulfide, 1 x 10(-4) mug/L air for methyl mercaptan, 1 x 10(-3) mug/L air for butyric acid, 1 x 10

4 thesis of these classical analogues were the mercaptans 10 and 11, which were obtained from the corre

5 rious proportions of the hydroxyl-terminated mercaptan (11-mercapto-1-undecanol).

6 ulfide anion or sulfur-centered radical from mercaptan 6.

7 hanism of thiol-ene reactions between methyl mercaptan and a series of 12 alkenes: propene, methyl vi

8 ding trans-fused product from E-homoallyllic mercaptan and cis-fused product from Z-homoallyllic merc

9 volatile sulfur-based odorants such as alkyl mercaptans and alkyl sulfides.

10 and methionine yields ammonia, H(2)S, methyl mercaptan, and butyrate, which are capable of arresting

11 Sulfur compounds including H2S, methyl mercaptan, and dimethyl-mono-(di;tri) sulfide are import

12 VSC, and in particular methyl mercaptan, are therefore capable of inducing deleterious

13 results showed agreement of <0.6% for methyl mercaptan at 5, 10, 15, and 20 mumol/mol to the expected

14 (2-furfurylthiol), and struck flint (benzyl mercaptan), at nanogram-per-liter levels.

15 The rGOx was modified with benzyl mercaptan (BnSH) to improve the interaction with Pd clus

16 cting self-assembled monolayers of octadecyl mercaptan (C18) on the MALDI probe surface, we were able

17 Breath hydrogen sulfide (H2S) and methyl-mercaptan (CH3SH) concentrations are used as quantitativ

18 is family, hydrogen sulfide (H2S) and methyl mercaptan (CH3SH), are primarily responsible for mouth o

19 s are a class of organic sulfur derivatives (mercaptans) characterized by the presence of sulfhydryl

20 ercaptomethane-lyase, responsible for methyl mercaptan (CHSH) production by oral anaerobes.

21 e to release back hydrogen sulfide and other mercaptans during AR-aging.

22 d sensitivity were hydrogen sulfide > methyl mercaptan > dimethylsulfide.

23 However, methyl mercaptan has the greatest effect.

24 ompounds such as hydrogen sulfide and methyl mercaptan have been associated with adult periodontitis

25 (Pd(0)-catalyzed thiol coupling) leading to mercaptan intermediate 18.

26 Data show that 48-hour exposure to mercaptan lowered resting intracellular pH but did not c

27 ort the hypothesis that gases such as methyl mercaptan may play a role in both surgical wound healing

28 atile compounds, volatile sulphur compounds, mercaptans, metals, anions and cations.

29 e been either a mixture of thiophenol/benzyl mercaptan, or the alkanethiol MESNA.

30 After cryogenically trapping the methyl mercaptan output stream from the permeation system into

31 aziridines with 2-bromobenzyl alcohols and -mercaptan, respectively, followed by Cu-catalyzed N-aryl

32 ment of inactivated enzyme with DTT or other mercaptans restores enzyme activity and reverses the cov

33 to dithiocarbamates (by facile addition of a mercaptan such as N-acetylcysteine) and quantitating the

34 derivatives from the coupling of homoallylic mercaptans such as hex-3-ene-1,6-dithiol with various al

35 distinguished as different classes, such as mercaptans, sulfides, thiophenes, benzothiophenes, and d

36 ve demonstrated that cells exposed to methyl mercaptan synthesize less collagen, degrade more collage

37 se the reactivity and facilitate addition of mercaptans, thereby raising inducer potencies.

38 atives involving conjugate addition of allyl mercaptan to an acrylate containing a tethered olefinic

39 e permeation tube was replaced with a methyl mercaptan tube (a toxic, reactive compound) in balance n

40 the presence of allyl alcohol and tert-butyl mercaptan undergo nucleophilic substitution followed by

41 he headspace above water spiked with dibutyl mercaptan was sampled with a solid phase microextraction

42 Hydrogen sulfide and methyl mercaptan were derivatized under a more stable N-ethyl m

43 he reaction of both cis- and trans-homoallyl mercaptans with aldehydes provided the same major diaste

44 cyclizations between homoallyl alcohols and mercaptans with aldehydes.

45 tions between a representative thiol (methyl mercaptan) with N-allyl and N-propargyl maleimide under

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