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1α,4aα-(Carbonyloxymethylene)-1β-methyl-8-methylenegibbane-10β-carboxylic acid, also known as Gibberellin A15, is a derivative of the plant hormone Gibberellin. It plays a crucial role in regulating growth and various developmental processes in plants. The chemical structure of 1α,4aα-(Carbonyloxymethylene)-1β-methyl-8-methylenegibbane-10β-carboxylic acid allows it to interact with plant cells and influence their growth and development.

13744-18-8

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13744-18-8 Usage

Uses

Used in Agricultural Industry:
1α,4aα-(Carbonyloxymethylene)-1β-methyl-8-methylenegibbane-10β-carboxylic acid is used as a growth regulator for promoting plant growth and development. It helps in increasing the size and weight of fruits, vegetables, and other crops, leading to higher yields and improved quality.
Used in Plant Biotechnology:
In plant biotechnology, 1α,4aα-(Carbonyloxymethylene)-1β-methyl-8-methylenegibbane-10β-carboxylic acid is used as a tool to study the molecular mechanisms underlying plant growth and development. By manipulating the levels of 1α,4aα-(Carbonyloxymethylene)-1β-methyl-8-methylenegibbane-10β-carboxylic acid in genetically modified plants, researchers can gain insights into the complex regulatory networks that control these processes.
Used in Plant Hormone Research:
1α,4aα-(Carbonyloxymethylene)-1β-methyl-8-methylenegibbane-10β-carboxylic acid is used as a research compound in the field of plant hormone research. It helps scientists understand the role of Gibberellins in plant growth and development, as well as their interactions with other plant hormones and signaling pathways.
Used in Plant Breeding:
In plant breeding, 1α,4aα-(Carbonyloxymethylene)-1β-methyl-8-methylenegibbane-10β-carboxylic acid can be used to develop new plant varieties with improved growth characteristics, such as increased height, larger fruits, or enhanced resistance to environmental stresses. By incorporating 1α,4aα-(Carbonyloxymethylene)-1β-methyl-8-methylenegibbane-10β-carboxylic acid into breeding programs, plant breeders can create crops that are better suited to specific growing conditions or市场需求 (market demands).

Check Digit Verification of cas no

The CAS Registry Mumber 13744-18-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,4 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13744-18:
(7*1)+(6*3)+(5*7)+(4*4)+(3*4)+(2*1)+(1*8)=98
98 % 10 = 8
So 13744-18-8 is a valid CAS Registry Number.

13744-18-8Downstream Products

13744-18-8Relevant academic research and scientific papers

Influence of electron transport proteins on the reactions catalyzed by Fusarium fujikuroi gibberellin monooxygenases

Troncoso, Claudia,Carcamo, Jose,Hedden, Peter,Tudzynski, Bettina,Cecilia Rojas

, p. 672 - 683 (2008/09/19)

The multifunctional cytochrome P450 monooxygenases P450-1 and P450-2 from Fusarium fujikuroi catalyze the formation of GA14 and GA4, respectively, in the gibberellin (GA)-biosynthetic pathway. However, the activity of these enzymes is qualitatively and quantitatively different in mutants lacking the NADPH:cytochrome P450 oxidoreductase (CPR) compared to CPR-containing strains. 3β-Hydroxylation, a major P450-1 activity in wild-type strains, was strongly decreased in the mutants relative to oxidation at C-6 and C-7, while synthesis of C19-GAs as a result of oxidative cleavage of C-20 by P450-2 was almost absent whereas the C-20 alcohol, aldehyde and carboxylic acid derivatives accumulated. Interaction of the monooxygenases with alternative electron transport proteins could account for these different product distributions. In the absence of CPR, P450-1 activities were NADH-dependent, and stimulated by cytochrome b5 or by added FAD. These properties as well as the decreased efficiency of P450-1 and P450-2 in the mutants are consistent with the participation of cytochrome b5:NADH cytochrome b5 reductase as redox partner of the gibberellin monooxygenases in the absence of CPR. We provide evidence, from either incubations of GA12 (C-20 methyl) with cultures of the mutant suspended in [18O]H2O or maintained under an atmosphere of [18O]O2:N2 (20:80), that GA15 (C-20 alcohol) and GA24 (C-20 aldehyde) are formed directly from dioxygen and not from hydrolysis of covalently enzyme-bound intermediates. Thus these partially oxidized GAs correspond to intermediates of the sequential oxidation of C-20 catalyzed by P450-2.

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