C8754
硫胺素焦磷酸
≥95%, powder
别名:
氯化硫胺素焦磷酸酯, 硫胺素焦磷酸, 辅羧酶
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关于此项目
经验公式（希尔记法）:
C12H19ClN4O7P2S
化学文摘社编号:
分子量:
460.77
NACRES:
NA.54
PubChem Substance ID:
UNSPSC Code:
12352204
EC Number:
205-836-1
MDL number:
Beilstein/REAXYS Number:
3875902
产品名称
硫胺素焦磷酸, ≥95%
InChI
1S/C12H18N4O7P2S.ClH/c1-8-11(3-4-22-25(20,21)23-24(17,18)19)26-7-16(8)6-10-5-14-9(2)15-12(10)13;/h5,7H,3-4,6H2,1-2H3,(H4-,13,14,15,17,18,19,20,21);1H
InChI key
YXVCLPJQTZXJLH-UHFFFAOYSA-N
SMILES string
CC1=C(CCOP(OP(O)(O)=O)(O)=O)SC=[N+]1CC2=C(N)N=C(C)N=C2.[Cl-]
assay
≥95%
form
powder
solubility
H2O: soluble 50 mg/mL, clear to very slightly hazy, colorless
storage temp.
−20°C
Quality Level
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Application
Sigma的硫胺素焦磷酸用作底物，以检测从大鼠组织分离的高尔基体片层中的酶。
硫胺焦磷酸盐已被用于：
- 制备壳聚糖纳米粒子
- 在高性能
- 液相色谱（HPLC）分析中，作为维生素B1及其衍生物的标准品
- 免疫荧光
Biochem/physiol Actions
硫胺焦磷酸盐（TPP）是一种转酮醇酶的辅酶，可催化5-磷酸核糖的裂解。该反应可生成D-甘油醛-3-磷酸。该反应需要加入受体醛，例如核糖-5-磷酸、甘油醛或乙醇醛。TPP能够在′受体醛′存在下使羟基丙酮酸脱羧。
signalword
Warning
hcodes
Hazard Classifications
Skin Sens. 1
存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Racker E, et al.
Journal of the American Chemical Society, 75(4), 1010-1011 (1953)
Nucleosidediphosphatase activity in the Golgi apparatus and its usefulness for cytological studies.
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Proceedings of the National Academy of Sciences of the United States of America, 47, 802-810 (1961-06-15)
Immunofluorescence Analysis of Human Endocervical Tissue Explants Infected with Neisseria gonorrhoeae
Wang LC, et al.
Bio-protocol, 8(3) (2018)
Enhancement of thiamine release during synthetic mutualism between Chlorella sorokiniana and Azospirillum brasilense growing under stress conditions
Palacios OA, et al.
Journal of Applied Phycology, 28(3), 1521-1531 (2016)
Michael Moulin et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(36), 14622-14627 (2013-08-21)
Thiamin (vitamin B1) is an essential micronutrient needed as a cofactor for many central metabolic enzymes. Animals must have thiamin in their diet, whereas bacteria, fungi, and plants can biosynthesize it de novo from the condensation of a thiazole and
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