您当前所在的位置:首页 > 产品中心 > 产品详细信息
77-06-5 分子结构
点击图片或这里关闭

(1R,2R,5S,8S,9S,10R,11R,12S)-5,12-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadec-13-ene-9-carboxylic acid

ChemBase编号:119594
分子式:C19H22O6
平均质量:346.37438
单一同位素质量:346.14163842
SMILES和InChIs

SMILES:
[C@@]123[C@@H]([C@@](C(=O)O1)([C@H](C=C3)O)C)[C@@H]([C@]13[C@H]2CC[C@](C1)(C(=C)C3)O)C(=O)O
Canonical SMILES:
OC(=O)[C@H]1[C@H]2[C@]3([C@H]4[C@]51CC(=C)[C@](C5)(O)CC4)C=C[C@@H]([C@]2(C)C(=O)O3)O
InChI:
InChI=1S/C19H22O6/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/h4,6,10-13,20,24H,1,3,5,7-8H2,2H3,(H,21,22)/t10-,11+,12-,13-,16+,17+,18+,19-/m1/s1
InChIKey:
IXORZMNAPKEEDV-SNTJWBGVSA-N

引用这个纪录

CBID:119594 http://www.chembase.cn/molecule-119594.html

Collapse All Expand All

名称和登记号

名称和登记号

名称 登记号
IUPAC标准名
(1R,2R,5S,8S,9S,10R,11R,12S)-5,12-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadec-13-ene-9-carboxylic acid
IUPAC传统名
(1R,2R,5S,8S,9S,10R,11R,12S)-5,12-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadec-13-ene-9-carboxylic acid
gibberellin A3
别名
Berelex
Gibrescol
Gibberellin A3
Gibrofit
Activol
GA3
Gibberellic acid
(1S,2S,4aR,4bR,7S,9aS,10S,10aR)-2,7-dihydroxy-1-methyl-8-methylene-13-oxo-1,2,4b,5,6,7,8,9,10,10a-decahydro-4a,1-(epoxymethano)-7,9a-methanobenzo[a]azulene-10-carboxylic acid
CAS号
77-06-5
PubChem SID
162107687
PubChem CID
9819600

数据来源

数据来源

所有数据来源 商品来源 非商品来源
数据来源 数据ID
PubChem 9819600 external link

理论计算性质

理论计算性质

JChem
Acid pKa 4.163467  质子受体
质子供体 LogD (pH = 5.5) -1.0024102 
LogD (pH = 7.4) -2.7070677  Log P 0.3509133 
摩尔折射率 86.4155 cm3 极化性 34.211063 Å3
极化表面积 104.06 Å2 可自由旋转的化学键
里宾斯基五规则 true 

分子性质

分子性质

药理学性质 产品相关信息 生物活性(PubChem)
生物活性机理
Plant growth factor. expand 查看数据来源
Stimulates the cells of germinating seeds to produce mRNA molecules that code for hydrolytic enzymes expand 查看数据来源
生物来源
Produced by Gibberella fujikuroi and present in higher plants expand 查看数据来源
应用领域
Plant growth regulator expand 查看数据来源
Used as an experimental research mutagen expand 查看数据来源
Used in malting of barley expand 查看数据来源

详细说明

详细说明

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • Aldrich Library of 13C and 1H FT NMR Spectra, 1992, 1, 1145B, (nmr)
  • Aldrich Library of FT-IR Spectra, 1st edn., 1985, 1, 703A, (ir)
  • Cross, B.E. et al., Chem. Comm., 1965, 535, (biosynth)
  • McCapra, F. et al., J.C.S.(C), 1966, 1577, (cryst struct)
  • Schreiber, K. et al., Phytochemistry, 1966, 5, 1221, (isol)
  • Verbiscar, A.J. et al., Phytochemistry, 1967, 7, 807, (biosynth)
  • Yamaguchi, I. et al., Agric. Biol. Chem., 1970, 34, 1439, (deriv)
  • Yokota, T. et al., Agric. Biol. Chem., 1971, 35, 583, (isol)
  • Dawson, R.M. et al., Phytochemistry, 1975, 14, 2593, (biosynth)
  • Hook, J.M. et al., J.A.C.S., 1980, 102, 6628, (synth)
  • Corey, E.J. et al., J.A.C.S., 1982, 104, 6129, (synth)
  • Kutschabsky, L. et al., J.C.S. Perkin 1, 1983, 1653, (cryst struct)
  • Schwartz, E. et al., Pharmazie, 1983, 38, 716, (pharmacol)
  • Al-Ekabi, H.K. et al., Can. J. Chem., 1984, 62, 1996, (ms)
  • Hook, J.N. et al., J.O.C., 1984, 49, 3250, (synth)
  • Lewer, P. et al., Phytochemistry, 1984, 23, 2803, (biosynth)
  • Danheiser, R.L., Strategies Tactics Org. Synth., 1984, 21; CA, 102, 6856, (book)
  • Synform, 1984, 2, 197, (rev)
  • Hossain, M.B. et al., Acta Cryst. C, 1988, 44, 1022, (cryst struct)
  • Pesticide Manual, 9th edn., 1991, No. 6910
  • Bhaskar, K.V. et al., Tet. Lett., 1991, 32, 6203, (GA85, GA86)
  • Agrochemicals Handbook, 3rd edn., Royal Society of Chemistry, 1992, A797
  • Sheng, C. et al., Biosci., Biotechnol., Biochem., 1992, 56, 564, (isol, GA85)
  • Blake, P.S. et al., Phytochemistry, 1993, 32, 781, (GA87)
  • Lewis, R.J., Sax's Dangerous Properties of Industrial Materials, 8th edn., Van Nostrand Reinhold, 1992, GEM000
正在搜索,请耐心等待...(如果遇到网页错误或者长时间没有结果,请刷新页面[F5])

专利

专利

PubChem iconPubChem Patent Google Patent Search IconGoogle Patent

互联网资源

互联网资源

百度图标百度 google iconGoogle