Category: 129830-38-2

Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 129830-38-2, Name is Y-27632 dihydrochloride, SMILES is O=C([C@H]1CC[C@H]([C@H](N)C)CC1)NC2=CC=NC=C2.[H]Cl.[H]Cl, belongs to indole-building-block compound. In a document, author is Ben Khedher, Saoussen, introduce the new discover, Computed Properties of C14H23Cl2N3O.

Biological potential of Bacillus subtilis V26 for the control of Fusarium wilt and tuber dry rot on potato caused by Fusarium species and the promotion of plant growth

Fusariosis of potato caused by the Fusarium spp. is one of the most destructive soil-borne diseases throughout the world. This study aimed to investigate the growth-promoting and biocontrol potential of Bacillus subtilis V26 against the causal agents of Fusarium wilt and Fusarium dry rot diseases on potato. Characterization of plant growth promoting traits was assessed in vitro. The strain V26 was able to fix nitrogen, to produce indole-3-acetic acid, siderophore, hydrolytic enzymes and to solubilize inorganic phosphate. The PCR detection of ituC, fenA, fenB, fenD, srfAA, bmy, mnlA, bae and bac genes coding for iturin, fengycin, surfactin, bacyllomicin, macrolactin, bacillaene and bacilysin indicated a potential for lipopeptides, polyketides and dipeptide production, respectively by the strain V26. In vitro antagonism test showed that this strain can effectively inhibit F. oxysporum, F. solani, F. gramineaurum and F. sambucinum growth by 54.7 to 85.3% as compared to the untreated control, in a dual method. Antifungal activity was demonstrated against the dry rot potato tubers caused by Fusarium species. The preventive application of V26 significantly decreased the Fusarium dry rot disease severity at 42.8-63.8%, after 21 days of fungi inoculation. After 15 days of seedling emergence, plants were irrigated with V26 spore suspensions (108 CFU/mL), prior infection by Fusaium species, Fusarium wilt severity were reduced by 54.8 to 60.8% and plant growth parameters were improved, compared to the untreated ones, 60 days post-inoculation. Therefore, this strain could be a promising candidate to be developed as commercial biofertilizer and biocontrol formulation in sustainable agriculture.

The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 129830-38-2 is helpful to your research. Computed Properties of C14H23Cl2N3O.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Related Products of 129830-38-2, Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, 129830-38-2, Name is Y-27632 dihydrochloride, SMILES is O=C([C@H]1CC[C@H]([C@H](N)C)CC1)NC2=CC=NC=C2.[H]Cl.[H]Cl, belongs to indole-building-block compound. In a article, author is Chirkova, Zh. V., introduce new discover of the category.

Synthesis of Substituted 2-Oxo-2,3-dihydro-1H-imidazo-[1,2-a]indole-6,7-dicarbonitriles

A three-step procedure has been developed for the synthesis of 2-oxo-2,3-dihydro-1H-imidazo-[1,2-a]indole-6,7-dicarbonitriles from substituted 2-amino-1-hydroxy-1H-indole-5,6-dicarbonitriles.

Related Products of 129830-38-2, Consequently, the presence of a catalyst will permit a system to reach equilibrium more quickly, but it has no effect on the position of the equilibrium as reflected in the value of its equilibrium constant.I hope my blog about 129830-38-2 is helpful to your research.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Application of 129830-38-2, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 129830-38-2, Name is Y-27632 dihydrochloride, SMILES is O=C([C@H]1CC[C@H]([C@H](N)C)CC1)NC2=CC=NC=C2.[H]Cl.[H]Cl, belongs to indole-building-block compound. In a article, author is Budaev, A. B., introduce new discover of the category.

From 1,2,5-Oxadiazolo[3,4-g]indoles to Pyrrolo[2,3-f]quinoxalines in One Preparative Stage

Pyrrolo[2,3-f]quinoxalines are synthesized by heating 1,2,5-oxadiazolo[3,4-g]indoles with ethanolamine in the presence of p-toluenesulfonic acid.

Application of 129830-38-2, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 129830-38-2.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

In an article, author is Deng, Yan, once mentioned the application of 129830-38-2, SDS of cas: 129830-38-2, Name is Y-27632 dihydrochloride, molecular formula is C14H23Cl2N3O, molecular weight is 320.26, MDL number is MFCD03490488, category is indole-building-block. Now introduce a scientific discovery about this category.

Three New Indole Alkaloids from Tabernaemontana divaricata

Three new monoterpene indole alkaloids, 3a-hydroxymethyl-ibogamine (1), 3 alpha-acetatemethoxyl-ibogamine (2), 16 alpha-hydroxyl-ibogamine (3) together with six known alkaloids were isolated from the branches and leaves of Tabernaemontana divaricata (Apocynaceae). The structures of these alkaloids were determined by spectroscopic analyses. All isolated compounds showed no significant cytotoxicity against SGC-7901 gastric cancer, HeLa, and A-549 lung cancer cell lines (IC50 > 20 mu M). [GRAPHICS] .

If you are interested in 129830-38-2, you can contact me at any time and look forward to more communication. SDS of cas: 129830-38-2.

Reference:
Indole alkaloid derivatives as building blocks of natural products from?Bacillus thuringiensis?and?Bacillus velezensis?and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles