Gibberellin A1 (BioDeep_00000396959)

   

PANOMIX_OTCML-2023


代谢物信息卡片


4a?,4b?-Gibbane-1?,10?-dicarboxylic acid, 2?,4a,7-trihydroxy-1-methyl-8-methylene-, 1,4a-lactone (8CI); 4a,1-(Epoxymethano)-7,9a-methanobenz[a]azulene, gibbane-1,10-dicarboxylic acid deriv.; (+)-Gibberillin A1; GA1; Giberellin A1

化学式: C19H24O6 (348.1572804)
中文名称: 赤霉素A1
谱图信息: 最多检出来源 Viridiplantae(plant) 1.29%

分子结构信息

SMILES: C=C1C[C@]23C[C@]1(CC[C@H]2[C@]12CC[C@@H]([C@](C)([C@H]1[C@@H]3C(=O)O)C(=O)O2)O)O
InChI: InChI=1S/C19H24O6/c1-9-7-17-8-18(9,24)5-3-10(17)19-6-4-11(20)16(2,15(23)25-19)13(19)12(17)14(21)22/h10-13,20,24H,1,3-8H2,2H3,(H,21,22)/t10-,11+,12-,13-,16-,17+,18+,19-/m1/s1

描述信息

Gibberellin A1 is a C19-gibberellin, initially identified in Gibberella fujikuroi. It has a role as a plant metabolite. It is a lactone, a gibberellin monocarboxylic acid and a C19-gibberellin. It is a conjugate acid of a gibberellin A1(1-).
Gibberellin A1 is a natural product found in Thlaspi arvense, Populus candicans, and other organisms with data available.
D006133 - Growth Substances > D010937 - Plant Growth Regulators > D005875 - Gibberellins
A C19-gibberellin, initially identified in Gibberella fujikuroi.
Gibberellin a1, also known as ga1, is a member of the class of compounds known as c19-gibberellin 6-carboxylic acids. C19-gibberellin 6-carboxylic acids are c19-gibberellins with a carboxyl group at the 6-position. Thus, gibberellin a1 is considered to be an isoprenoid lipid molecule. Gibberellin a1 is slightly soluble (in water) and a weakly acidic compound (based on its pKa). Gibberellin a1 can be found in a number of food items such as elderberry, enokitake, black salsify, and new zealand spinach, which makes gibberellin a1 a potential biomarker for the consumption of these food products.

同义名列表

10 个代谢物同义名

4a?,4b?-Gibbane-1?,10?-dicarboxylic acid, 2?,4a,7-trihydroxy-1-methyl-8-methylene-, 1,4a-lactone (8CI); 4a,1-(Epoxymethano)-7,9a-methanobenz[a]azulene, gibbane-1,10-dicarboxylic acid deriv.; (+)-Gibberillin A1; GA1; Giberellin A1; (1S,2S,4aR,4bR,7S,9aS,10S,10aR)-2,7-Dihydroxy-1-methyl-8-methylene-13-oxododecahydro-4a,1-(epoxymethano)-7,9a-methanobenzo[a]azulene-10-carboxylic acid; (1R,2R,5S,8S,9S,10R,11S,12S)-5,12-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1(5,8).0(1,10).0(2,8)]heptadecane-9-carboxylic acid; 2beta,7alpha-dihydroxy-1beta-methyl-8-methylidene-13-oxo-4a,1alpha-epoxymethano-4aalpha,4bbeta-gibbane-10beta-carboxylic acid; (1alpha,2beta,4aalpha,4bbeta,10beta)-2,4a,7-Trihydroxy-1-methyl-8-methylenegibbane-1,10-dicarboxylic acid 1,4a-lactone; Gibberellin A1 100 microg/mL in Acetonitrile; gibberellin A(1); Gibberellin A1; Gibberellin 1; GA1



数据库引用编号

10 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(2)

代谢反应

130 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(3)

INOH(0)

PlantCyc(127)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

4 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:

  • PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。



文献列表

  • Pedro M Hernández, Carlos A Arango, Soo-Kyung Kim, Andres Jaramillo-Botero, William A Goddard. Predicted Three-Dimensional Structure of the GCR1 Putative GPCR in Arabidopsis thaliana and Its Binding to Abscisic Acid and Gibberellin A1. Journal of agricultural and food chemistry. 2023 Apr; 71(14):5770-5782. doi: 10.1021/acs.jafc.2c06846. [PMID: 36977192]
  • Zhong-Feng Li, Yong Guo, Lin Ou, Huilong Hong, Jun Wang, Zhang-Xiong Liu, Bingfu Guo, Lijuan Zhang, Lijuan Qiu. Identification of the dwarf gene GmDW1 in soybean (Glycine max L.) by combining mapping-by-sequencing and linkage analysis. TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik. 2018 May; 131(5):1001-1016. doi: 10.1007/s00122-017-3044-8. [PMID: 29550969]
  • Jordi Bou-Torrent, Jaime F Martínez-García, José Luis García-Martínez, Salomé Prat. Gibberellin A1 metabolism contributes to the control of photoperiod-mediated tuberization in potato. PloS one. 2011; 6(9):e24458. doi: 10.1371/journal.pone.0024458. [PMID: 21961036]
  • Leonid V Kurepin, R J Neil Emery, Richard P Pharis, David M Reid. Uncoupling light quality from light irradiance effects in Helianthus annuus shoots: putative roles for plant hormones in leaf and internode growth. Journal of experimental botany. 2007; 58(8):2145-57. doi: 10.1093/jxb/erm068. [PMID: 17490995]
  • Mami Sugano, Yuriko Nakagawa, Hiroshi Nyunoya, Teruko Nakamura. Expression of gibberellin 3 beta-hydroxylase gene in a gravi-response mutant, weeping Japanese flowering cherry. Uchu Seibutsu Kagaku. 2004 Dec; 18(4):261-6. doi: 10.2187/bss.18.261. [PMID: 15858394]
  • Carla M Wolbang, Peter M Chandler, Jennifer J Smith, John J Ross. Auxin from the developing inflorescence is required for the biosynthesis of active gibberellins in barley stems. Plant physiology. 2004 Feb; 134(2):769-76. doi: 10.1104/pp.103.030460. [PMID: 14730077]
  • Damian P O'Neill, John J Ross. Auxin regulation of the gibberellin pathway in pea. Plant physiology. 2002 Dec; 130(4):1974-82. doi: 10.1104/pp.010587. [PMID: 12481080]
  • M Taneyama, T Okamoto, H Yamane, T Minamikawa. Involvement of gibberellins in expression of a cysteine proteinase (SH-EP) in cotyledons of Vigna mungo seedlings. Plant & cell physiology. 2001 Nov; 42(11):1290-3. doi: 10.1093/pcp/pce153. [PMID: 11726715]
  • F D Cassán, C D Lucangeli, R Bottini, P N Piccoli. Azospirillum spp. metabolize [17,17-2H2]gibberellin A20 to [17,17-2H2]gibberellin A1 in vivo in dy rice mutant seedlings. Plant & cell physiology. 2001 Jul; 42(7):763-7. doi: 10.1093/pcp/pce099. [PMID: 11479384]
  • M Huanpu, P S Blake, G Browning, J M Taylor. Metabolism of gibberellins A1 and A3 in fruits and shoots of Prunus avium. Phytochemistry. 2001 Jan; 56(1):67-76. doi: 10.1016/s0031-9422(00)00354-x. [PMID: 11198821]