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地塞米松 21-磷酸

更新时间:2025-08-26 07:10:15

地塞米松 21-磷酸结构式
地塞米松 21-磷酸结构式
品牌特惠专场
常用名 地塞米松 21-磷酸 英文名 Dexamethasone Phosphate
CAS号 312-93-6 分子量 472.44100
密度 1.45g/cm3 沸点 669.6ºC at 760mmHg
分子式 C22H30FO8P 熔点 154-157°C (lit.)
MSDS N/A 闪点 358.7ºC

 地塞米松 21-磷酸用途


Dexamethasone phosphate (Dexamethasone 21-phosphate) 是一种无生物活性的化合物,可通过红细胞内酶进行去磷酸化。活性代谢物地塞米松随后通过细胞膜的简单被动扩散释放到循环中。Dexamethasone phosphate 包裹的红细胞具有用于类固醇依赖性溃疡性结肠炎研究的潜力。

 地塞米松 21-磷酸名称

中文名 地塞米松磷酸酯
英文名 dexamethasone phosphate
英文别名 更多

 地塞米松 21-磷酸生物活性

描述 Dexamethasone phosphate (Dexamethasone 21-phosphate) 是一种无生物活性的化合物,可通过红细胞内酶进行去磷酸化。活性代谢物地塞米松随后通过细胞膜的简单被动扩散释放到循环中。Dexamethasone phosphate 包裹的红细胞具有用于类固醇依赖性溃疡性结肠炎研究的潜力。
相关类别
参考文献

[1]. Fabrizio Bossa, et al. Erythrocytes-mediated delivery of dexamethasone 21-phosphate in steroid-dependent ulcerative colitis: a randomized, double-blind Sham-controlled study. Inflamm Bowel Dis. 2013 Aug;19(9):1872-9.  

 地塞米松 21-磷酸物理化学性质

密度 1.45g/cm3
沸点 669.6ºC at 760mmHg
熔点 154-157°C (lit.)
分子式 C22H30FO8P
分子量 472.44100
闪点 358.7ºC
精确质量 472.16600
PSA 151.17000
LogP 2.01270
InChIKey VQODGRNSFPNSQE-CXSFZGCWSA-N
SMILES CC1CC2C3CCC4=CC(=O)C=CC4(C)C3(F)C(O)CC2(C)C1(O)C(=O)COP(=O)(O)O
外观性状 白色至浅棕色固体
折射率 1.594
储存条件 通风低温干燥

 地塞米松 21-磷酸毒性和生态

 地塞米松 21-磷酸安全信息

危害码 (欧洲) Xn
风险声明 (欧洲) 62
海关编码 2937290090

 地塞米松 21-磷酸合成线路

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地塞米松 21-磷酸结构式

地塞米松 21-磷酸

312-93-6

文献:Chemical and Pharmaceutical Bulletin, , vol. 22, # 7 p. 1439 - 1450

 地塞米松 21-磷酸上下游产品

地塞米松 21-磷酸上游产品  1

地塞米松 21-磷酸下游产品  0

 地塞米松 21-磷酸海关

海关编码 2937290090

 地塞米松 21-磷酸靶点实验

查看更多实验

实验名称:Binding affinity towards human ADRA2A in an in vitro assay with cellular components m...
来源:ChEMBL
靶标:Alpha-2A adrenergic receptor
External Id:CHEMBL5291736
实验名称:Binding affinity towards human GABRA1 in an in vitro assay with cellular components m...
来源:ChEMBL
靶标:Gamma-aminobutyric acid receptor subunit gamma-2
External Id:CHEMBL5291799
实验名称:Binding affinity towards human PGR in an in vitro assay with cellular components meas...
来源:ChEMBL
靶标:Progesterone receptor
External Id:CHEMBL5291863
实验名称:Antagonist activity at human ADRA1A in an in vitro cell-based assay measured by fluor...
来源:ChEMBL
靶标:Alpha-1A adrenergic receptor
External Id:CHEMBL5291731
实验名称:Binding affinity towards human ESR1 in an in vitro cell free assay (CRO assay) measur...
来源:ChEMBL
靶标:Estrogen receptor
External Id:CHEMBL5291792
实验名称:Binding affinity towards human ADORA3 (agonistic activity) in an in vitro assay with ...
来源:ChEMBL
靶标:Adenosine receptor A3
External Id:CHEMBL5291728
实验名称:Compound was evaluated for inhibition of human PDE3A in an in vitro cell free assay m...
来源:ChEMBL
靶标:cGMP-inhibited 3',5'-cyclic phosphodiesterase 3A
External Id:CHEMBL5291856
实验名称:Binding affinity towards human OPRM1 in an in vitro assay with cellular components me...
来源:ChEMBL
靶标:Mu-type opioid receptor
External Id:CHEMBL5291855
实验名称:Agonist activity at human ADRA1A in an in vitro cell-based assay (CRO assay) measured...
来源:ChEMBL
靶标:Alpha-1A adrenergic receptor
External Id:CHEMBL5291730
实验名称:Compound was evaluated for inhibition of human F2 in an in vitro cell free assay meas...
来源:ChEMBL
靶标:Prothrombin
External Id:CHEMBL5291794
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 地塞米松 21-磷酸英文别名

Hexadrol phosphate
dexamethasone-21-phosphate
Dexamethasone 21-orthophosphate
Betnelan phosphate
Dexamethasone-21-dihydrogen-phosphate
Wymesone
Neodecadron
Oradexon phosphate
Dexamethasone phosphate
[2-[(8S,9R,10S,11S,13S,14S,16R,17R)-9-fluoro-11,17-dihydroxy-10,13,16-trimethyl-3-oxo-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-yl]-2-oxoethyl] dihydrogen phosphate
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