626-69-7 (O-硫-L-丝氨酸,H-Ser(SO3H)-OH)

快速询单

结构式：

O-硫-L-丝氨酸MOL文件

CAS号：

626-69-7

中文名称：

O-硫-L-丝氨酸

英文名称：

H-Ser(SO3H)-OH

分子式：

C₃H₇NO₆S

分子量：

185.155780076981

O-硫-L-丝氨酸(626-69-7)名称与标识符

名称

中文别名：

O-硫-L-丝氨酸;

英文别名：

L-Serine, O-sulfo-;(2S)-2-amino-3-sulfooxypropanoic acid;H-Ser(SO?H)-OH;H-Ser(SO₃H)-OH;O-Sulfo-L-serine;L-Serine O-sulfate;L-Serine,O-sulfo;L-serine-O-sulphate;L-Serin-O-sulfat;L-SOS;O-sulfonato-L-serine;Serine O-sulfate;serine sulfuric acid ester;

标识符

InChIKey：

LFZGUGJDVUUGLK-REOHCLBHSA-N

Inchi：

1S/C3H7NO6S/c4-2(3(5)6)1-10-11(7,8)9/h2H,1,4H2,(H,5,6)(H,7,8,9)/t2-/m0/s1

SMILES：

S(=O)(=O)([O-])OC[C@@H](C(=O)O)[NH3+]

O-硫-L-丝氨酸(626-69-7)物化性质

实验特性

LogP : -0.00120
PSA : 135.30000

计算特性

精确分子量 : 184.99900
氢键供体数量 : 3
氢键受体数量 : 7
可旋转化学键数量 : 4
重原子数量 : 11

O-硫-L-丝氨酸(626-69-7)推荐厂家更多厂家(5)

公司名称	手机号/电话	联系人	QQ	询单
上海瀚思化工有限公司	18939883912 021-34536277	顾经理	3003949364	询单
上海甄准生物科技有限公司	19301255008 021-68920155	徐经理19301255008	3004957527	询单
江苏艾康生物医药研发有限公司	18795912720 025-66061636	杨情情	3004779232	询单
上海瀚鸿化工有限公司	18918972708 021-54300995	戴遥	2355241816	询单
上海瀚鸿化工科技有限公司	13918533501 86-021-64541543	马道功	935888945	询单

O-硫-L-丝氨酸(626-69-7)相关文献

1. Serine O-sulfation probed by IRMPD spectroscopy
Roberto Paciotti,Cecilia Coletti,Nazzareno Re,Debora Scuderi,Barbara Chiavarino,Simonetta Fornarini,Maria Elisa Crestoni Phys. Chem. Chem. Phys. 2015 17 25891
2. Stereochemistry of conversion of the suicide substrates β-chloro-D-alanine-and D- and L-serine O-sulfates into pyruvate by D-amino acid aminotransferase and by L-aspartate aminotransferase
B. Svante Axelsson,Heinz G. Floss,Sungsook Lee,Ashraf Saeed,Philip A. Spencer,Douglas W. Young J. Chem. Soc. Perkin Trans. 1 1994 2137
3. Mechanisms and stereochemistry of the activation of (2S)- and (2R)-serine O-sulfate as suicide inhibitors for Escherichia coli glutamic acid decarboxylase
Janet E. Rose,Paul D. Leeson,David Gani J. Chem. Soc. Perkin Trans. 1 1994 3089
4. Mechanisms and stereochemistry of the activation of (2S)- and (2R)-serine O-sulfate as suicide inhibitors for Escherichia coli glutamic acid decarboxylase
Janet E. Rose,Paul D. Leeson,David Gani J. Chem. Soc. Chem. Commun. 1992 1784
5. A versatile synthesis of stereospecificaily labelled D-amino acids and related enzyme inhibitors
B. Svante Axelsson,Kevin J. O'Toole,Philip A. Spencer,Douglas W. Young J. Chem. Soc. Chem. Commun. 1991 1085
6. Racemases and epimerases operating through a 1,1-proton transfer mechanism: reactivity, mechanism and inhibition
Matthew D. Lloyd,Maksims Yevglevskis,Amit Nathubhai,Tony D. James,Michael D. Threadgill,Timothy J. Woodman Chem. Soc. Rev. 2021 50 5952
7. Recent advances in the formation of the bacterial peptidoglycan monomer unit
Jean van Heijenoort Nat. Prod. Rep. 2001 18 503
8. Catalytic mechanism and properties of pyridoxal 5′-phosphate independent racemases: how enzymes alter mismatched acidity and basicity
Conrad Fischer,Yeong-Chan Ahn,John C. Vederas Nat. Prod. Rep. 2019 36 1687
9. The stereochemical course of reactions catalysed by Escherichia coli glutamic acid decarboxylase
Kevin Tilley,Mahmoud Akhtar,David Gani J. Chem. Soc. Chem. Commun. 1992 68
10. The stereochemical course of reactions catalysed by Escherichia coli glutamic acid decarboxylase
Kevin Tilley,Mahmoud Akhtar,David Gani J. Chem. Soc. Chem. Commun. 1992 68