氯丝菌素

更新时间：2024-01-11 18:39:03

氯丝菌素结构式	常用名	氯丝菌素	英文名	chlorothricin
	CAS号	34707-92-1	分子量	955.479
	密度	1.4±0.1 g/cm3	沸点	1050.8±65.0 °C at 760 mmHg
	分子式	C₅₀H₆₃ClO₁₆	熔点	N/A
	MSDS	N/A	闪点	589.3±34.3 °C

氯丝菌素用途

氯菊酯是一种抗生素,是猪心苹果酸脱氢酶的抑制剂[1]。

中文名	氯丝菌素
英文名	Chlorothricin
英文别名	更多

描述	氯菊酯是一种抗生素,是猪心苹果酸脱氢酶的抑制剂[1]。
相关类别	研究领域 >> 感染研究领域 >> 炎症/免疫
参考文献	[1]. P W Schindler, et al. Chlorothricin, and inhibitor of porcine-heart malate dehydrogenases, discriminating between the mitochondrial and cytoplasmic isoenzyme. Eur J Biochem. 1975 Feb 21;51(2):579-85.

密度	1.4±0.1 g/cm3
沸点	1050.8±65.0 °C at 760 mmHg
分子式	C₅₀H₆₃ClO₁₆
分子量	955.479
闪点	589.3±34.3 °C
精确质量	954.380493
PSA	223.04000
LogP	9.13
蒸汽压	0.0±0.3 mmHg at 25°C
折射率	1.619

213122-67-9

~89%

氯丝菌素

34707-92-1

文献：Roush, William R.; Sciotti, Richard J. Journal of the American Chemical Society, 1998 , vol. 120, # 30 p. 7411 - 7419

213122-74-8

氯丝菌素

34707-92-1

文献：Roush, William R.; Sciotti, Richard J. Journal of the American Chemical Society, 1994 , vol. 116, # 14 p. 6457 - 6458

157944-74-6

氯丝菌素

34707-92-1

文献：Roush, William R.; Sciotti, Richard J. Journal of the American Chemical Society, 1994 , vol. 116, # 14 p. 6457 - 6458

未登录

157944-73-5

氯丝菌素

34707-92-1

文献：Roush, William R.; Sciotti, Richard J. Journal of the American Chemical Society, 1994 , vol. 116, # 14 p. 6457 - 6458

未登录

157944-72-4

氯丝菌素

34707-92-1

文献：Roush, William R.; Sciotti, Richard J. Journal of the American Chemical Society, 1994 , vol. 116, # 14 p. 6457 - 6458

213122-73-7

氯丝菌素

34707-92-1

文献：Roush, William R.; Sciotti, Richard J. Journal of the American Chemical Society, 1998 , vol. 120, # 30 p. 7411 - 7419

157944-69-9

氯丝菌素

34707-92-1

文献：Roush, William R.; Sciotti, Richard J. Journal of the American Chemical Society, 1998 , vol. 120, # 30 p. 7411 - 7419

未登录

157944-71-3

氯丝菌素

34707-92-1

文献：Roush, William R.; Sciotti, Richard J. Journal of the American Chemical Society, 1998 , vol. 120, # 30 p. 7411 - 7419

氯丝菌素上游产品 1
CAS号157944-69-9
氯丝菌素下游产品 0

Diuresal

(1S,3R,6R,7E,13R,16S,17S,21R,22R)-17-({4-O-[3-O-(3-Chloro-6-methoxy-2-methylbenzoyl)-2,6-dideoxy-β-D-arabino-hexopyranosyl]-2,6-dideoxy-β-D-arabino-hexopyranosyl}oxy)-28-hydroxy-3,22-dimethyl-23,26-dioxo-24,27-dioxapentacyclo[23.2.1.0.0.0]octacosa-4,7,14,25(28)-tetraene-4-carboxylic acid

Chlorothiazid

Chlotride

16a,19-metheno-18H-benzo[e]naphtho[2,1-m][1,4]dioxacyclopentadecin-14-carboxylic acid, 4-[[4-O-[3-O-(3-chloro-6-methoxy-2-methylbenzoyl)-2,6-dideoxy-β-D-arabino-hexopyranosyl]-2,6-dideoxy-β-D-arabino-hexopyranosyl]oxy]-1,2,3,4,4a,6a,7,8,9,10,12a,15,16,21,21a,21b-hexadecahydro-22-hydroxy-15,21a-dimethyl-18,21-dioxo-, (4S,4aS,6aR,11E,12aR,15R,16aS,21aR,21bR)-

chlorothiazide

Chlorthiazide

(1S,3R,6R,7E,13R,16S,17S,21R,22R)-17-({4-O-[3-O-(3-Chloro-6-methoxy-2-methylbenzoyl)-2,6-dideoxy-β-D-arabino-hexopyranosyl]-2,6-dideoxy-β-D-arabino-hexopyranosyl}oxy)-28-hydroxy-3,22-dimethyl-23 ,26-dioxo-24,27-dioxapentacyclo[23.2.1.0.0.0]octacosa-4,7,14,25(28)-tetraene-4-carboxylic acid

Diuril

chlorothricin

Chlorosal

Chlortiazid

Clotride

6-chloro-2H-1,2,4-benzothiadiazine-7-sulfonamide,1,1-dioxide

Chlorurit

16a,19-Metheno-18H-benzo[e]naphtho[2,1-m][1,4]dioxacyclopentadecin-14-carboxylic acid, 4-[[4-O-[3-O-(3-chloro-6-methoxy-2-methylbenzoyl)-2,6-dideoxy-β-D-arabino-hexopyranosyl]-2,6-dideoxy-β-D-ar abino-hexopyranosyl]oxy]-1,2,3,4,4a,6a,7,8,9,10,12a,15,16,21,21a,21b-hexadecahydro-22-hydroxy-15,21a-dimethyl-18,21-dioxo-, (4S,4aS,6aR,11E,12aR,15R,16aS,21aR,21bR)-