410 resultados para fluazifop-p-butil fomesafen


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2.5MaB.P.ODP11437ka3.02.0MaB.P.2.5MaB.P. ODP 1143922113172772m114313595m3.02.6 Ma B. P.3.02.0MaB.P. 13.02.6 Ma B. P. 2.62.0 Ma B. P.2.6 Ma B. P. 22.6 Ma B. P.- 33.02.0 Ma B. P.0.1 Ma46.9ka

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CNPC:N:PCN:PN:P 1603N:PNPlNP;2NPNP;3NPN:P A1980B1999NP0515305080 g NHN03.m.2.yr-1P024816and 32 g P2Osm-2 yr-1NN:PCN:PN 1NNpP2001APN;PN2000BNP(B2000)PN;NBNN:PA2000B2000PN:P 2N:P;AB;NPNAN:P 3NNAB; B;ANPNNPP < 0.005PP>0.05;ANPN:P;BN:P 4N(0-10 cm)N(10-20 cm)NiANPNP;BNP; NNPNPN:P 5(O-lO cm)10-20 cm;ArNPNP;BNC:NC:PN:P;N 6;200120002001;NNP;CNN:PC:P N:PNP;NP;NPNP NNPN (B)N(A)PNNPNN:P;PPC:NC

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1999CNP 6abababSLATilmanKnops pH1;;pH2;3;0-10cm;;

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CNPC:N:PCarex appendiculata(Stipa baicalensis)(Leymus chinensis)(Stipa grandis)(Caragana microphylla)(Artemisia frigid)(S. krylovii)(Ulmus Pumila)8273144C: N: PC:N:P 1. C:NN:PC:PC:N:P NP 2. C:N:PC:N:PCNPCPNCNP 3. CNPNN:PCC:NC:P 4. 5.

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Hemorrhagic toxins are widely distributed in viperid and crotalid snake venoms. Envenomation of Trimeresurus stejnegeri, a member of Crotalidae family, caused potent systemic and local hemorrhage. Up to now, there is no report on hemorrhage toxins from th

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A new metalloproteinase-disintegrin, named Jerdonitin, was purified from Trimeresurus jerdonii venom with a molecular weight of 36 kDa on SDS-PAGE. It dose-dependently inhibited ADP-induced human platelet aggregation with IC50 of 120 nM. cDNA cloning and sequencing revealed that Jerdonitin belonged to the class II of snake venom metalloproteinases (SVMPs) (P-II class). Different from other P-II class SVMPs, metalloproteinase and disintegrin domains of its natural protein were not separated, confirmed by internal peptide sequencing. Compared to other P-II class SVMPs, Jerdonitin has two additional cysteines (Cys219 and Cys238) located in the spacer domain and disintegrin domain, respectively. They probably form a disulfide bond and therefore the metalloproteinase and disintegrin domains cannot be separated by posttranslationally processing. In summary, comparison of the amino acid sequences of Jerdonitin with those of other P-II class SVMPs by sequence alignment and phylogenetic analysis, in conjunction with natural protein structure data, suggested that it was a new type of P-II class SVMPs. (C) 2003 Elsevier Inc. All rights reserved.

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To search for compounds with superior anti-human immunodeficiency virus type 1 (HIV-1) activity, ten 5,5'-(p-phenylenebisazo)-8-hydroxyquinoline sulfonates (4a-j) were synthesized and preliminarily evaluated as HIV-1 inhibitors in vitro for the first time. Some compounds demonstrated anti-HIV-1 activity, especially 5,5'-(p-phenylenebisazo)-8-hydroxyquinoline p-ethylbenzenesulfonate (4g) and 5,5'-(p-phenylenebisazo)-8-hydroxyquinoline p-chlorobenzenesulfonate (41) showed the more potent anti-HIV-1 activity with 50% effective concentration (EC50) values of 2.59 and 4.01 mu g/ml, and therapeutic index (TI) values of 31.77 and 24.51, respectively.

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--,P-,P

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