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6025-81-6 分子结构
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(2E)-2-methyl-4-[(9H-purin-6-yl)amino]but-2-en-1-ol

ChemBase编号:103578
分子式:C10H13N5O
平均质量:219.24312
单一同位素质量:219.11201006
SMILES和InChIs

SMILES:
C/C(=C\CNc1ncnc2c1[nH]cn2)/CO
Canonical SMILES:
OC/C(=C/CNc1ncnc2c1[nH]cn2)/C
InChI:
InChI=1S/C10H13N5O/c1-7(4-16)2-3-11-9-8-10(13-5-12-8)15-6-14-9/h2,5-6,16H,3-4H2,1H3,(H2,11,12,13,14,15)
InChIKey:
UZKQTCBAMSWPJD-UHFFFAOYSA-N

引用这个纪录

CBID:103578 http://www.chembase.cn/molecule-103578.html

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名称和登记号

名称和登记号

名称 登记号
IUPAC标准名
(2E)-2-methyl-4-[(9H-purin-6-yl)amino]but-2-en-1-ol
(2E)-2-methyl-4-[(7H-purin-6-yl)amino]but-2-en-1-ol
2-methyl-4-[(9H-purin-6-yl)amino]but-2-en-1-ol
2-methyl-4-[(7H-purin-6-yl)amino]but-2-en-1-ol
IUPAC传统名
trans-zeatin
zeatin
别名
6-(4-羟基-3-甲基丁-2-烯基氨基)嘌呤
N6-(4-羟基-3-甲基-2-丁烯-1-基)腺嘌呤
反-玉米素 盐酸盐
反-玉米素
6-(4-Hydroxy-3-methylbut-2-enylamino)purine
trans-Zeatin hydrochloride
Zeatin
N6-(4-Hydroxy-3-methyl-2-buten-1-yl)adenine
trans-Zeatin
(2E)-2-Methyl-4-(9H-purin-6-ylamino)-2-buten-1-ol
6-(4-Hydroxy-3-methyl-trans-2-butenylamino)purine
N6-(4-Hydroxy-3-methyl-trans-2-butenyl)adenine
ZT
ZTA
Zeatin
(E)-Zeatin
Zeatine
trans-Zeatin
6-[(E)-4-Hydroxy-3-methyl-2-butenylamino] purine
N6-(4-Hydroxy-3-methyl-2-buten-1-yl)adenine
6-[4-Hydroxy-3-methylbut-2-enylamino]purine
ZEATIN
CAS号
6025-81-6
32771-64-5
1637-39-4
13114-27-7
MDL号
MFCD00213654
Beilstein号
616241
PubChem SID
162090867
24902158
24902177
24902170
24890259
PubChem CID
449093

理论计算性质

理论计算性质

JChem
Acid pKa 9.867978  质子受体
质子供体 LogD (pH = 5.5) -0.2835231 
LogD (pH = 7.4) -0.15424982  Log P -0.14883372 
摩尔折射率 62.9856 cm3 极化性 22.93417 Å3
极化表面积 86.72 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

理化性质 安全信息 产品相关信息 生物活性(PubChem)
溶解度
H2O: soluble expand 查看数据来源
外观
off-white to yellow powder expand 查看数据来源
熔点
208-215°C expand 查看数据来源
保存条件
0°C expand 查看数据来源
2-8°C expand 查看数据来源
RTECS编号
EM9506000 expand 查看数据来源
MSDS下载
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
德国WGK号
3 expand 查看数据来源
个人保护装置
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand 查看数据来源
保存温度
-20°C expand 查看数据来源
纯度
>99.8% expand 查看数据来源
≥97% expand 查看数据来源
≥98.0% (HPLC) expand 查看数据来源
97% expand 查看数据来源
质检报告
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
适用性
plant cell culture tested expand 查看数据来源
品质说明
crystallized expand 查看数据来源
Empirical Formula (Hill Notation)
C10H13N5O expand 查看数据来源

详细说明

详细说明

MP Biomedicals MP Biomedicals Sigma Aldrich Sigma Aldrich TRC TRC
MP Biomedicals -  02153854 external link
(6-[(E)-4-Hydroxy-3-methyl-2-butenylamino] purine) Synthetic trans-isomer White, crystalline needles Purity: >99.8% by HPLC Highly potent growth hormone in plants. Stimulates cell division.
MP Biomedicals -  02152271 external link
cis-isomer
Off-white to yellow powder
May contain up to 10% trans-isomer.
Sigma Aldrich -  Z0164 external link
Other Notes
Mixed isomersApprox. 80% trans; balance primarily cis.
Application
Zeatin is a coconut milk-derived plant hormone (cytokinin) that promotes growth of lateral buds, stimulates cell division(Lateral Dominance), callus initiation and seed germination. Zeatin is used with Murashige and Skoog and other media, zeatin promotes multiple shoot generation from internodes and high frequency thick spread roots.
Sigma Aldrich -  Z0876 external link
Biochem/physiol Actions
trans-Zeatin-riboside is a plant cytokinin
Sigma Aldrich -  Z2753 external link
包装
5 mg in glass bottle
Sigma Aldrich -  96088 external link
Biochem/physiol Actions
trans-Zeatin-riboside is a plant cytokinin
Toronto Research Chemicals -  Z273000 external link
Zeatin, purified from Zea mays, is a member of the cytokinin group of plant growth factors, the activity of which is attributed to its more stable trans form. Trans-Zeatin inhibits UVB-induced matrix metalloproteinase-1 expression via MAP kinase signaling

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • Murashige, T., et al.: Physiol. Plant, 15, 473 (1962)
  • Brenneisen, P., et al.: J. Biol. Chem., 273, 5279 (1962)
  • Choi, M., et al.: J. Dermatol. Sci., 46, 127 (1962)
  • Bae, J., et al.: Food Chem. Toxicol., 46, 1298 (1962)
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专利

专利

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