Histakool; Clemizol; 1-(4-Chloro-Benzyl)-2-Pyrrolidin-1-Ylmethyl-1H-Benzoimidazole; 1-(P-Chlorobenzyl)-2-Pyrrolidylmethylenebenzimidazole; 1-(4-Chloro-Benzyl)-2-Pyrrolidinomethyl-1H-Benzimidazole; Histacur; 1-(4-Chlorobenzyl)-2-(Pyrrolidin-1-Ylmethyl)-1H-Benzimidazole; 1-(4-Chlor-Benzyl)-2-Pyrrolidinomethyl-1H-Benzimidazol; 1H-Benzimidazole,1-[(4-Chlorophenyl)Methyl]-2-(1-Pyrrolidinylmethyl); 1-[(4-Chlorophenyl)Methyl]-2-(Pyrrolidin-1-Ylmethyl)Benzimidazole; Clemizolum

Brief Introduction

Pyrrolidazole is also called 1 - [(4-chlorophenyl) methyl] - 2 - (pyrrolidine-1-ylmethyl) benzimidazole and krimidazole. It has antihistamine effect, moderate sedative effect and obvious antipruritic effect. The latest research shows that it has the effect of anti hepatitis C virus. This product can prolong the effective refractory period of atrial muscle, and it has been reported to treat atrial flutter. Side effects are rare.

Ethyl [(2R,3S,4S,5R,6S)-3,4,5-Trihydroxy-6-[5-Methyl-1-Propan-2-Yl-4-[(4-Propan-2-Yloxyphenyl)Methyl]Pyrazol-3-Yl]Oxyoxan-2-Yl]Methyl Carbonate

MSDS

CAS:442201-24-3

Molecular Formula:C26H38N2O9

Alias

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Kgt-1681; Remogliflozin Etabonate; Unii-Tr0Qt6Qsul; Remogliflozin Etabonate (Usan/Inn); Gsk-189075; Tr0Qt6Qsul

Brief Introduction

Remogliflozin Etabonate is an orally available prodrug of remogliflozin, a benzylpyrazole glucoside-based inhibitor of renal sodium-glucose co-transporter subtype 2 (SGLT2) with antihyperglycemic activity. Upon administration and absorption, the inactive prodrug is converted to its active form remogliflozin and acts selectively on the sodium-glucose co-transporter subtype 2 (SGLT2).

Tabersonine

MSDS

CAS:4429-63-4

Molecular Formula:C21H24N2O2

Alias

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Aspidospermidine-3-Carboxylicacid,2,3,6,7-Tetrahydro-,Methylester,(5-Alpha; Aspidospermidine-3-Carboxylic Acid, 2,3,6,7-Tetradehydro-, Methyl Ester, (5Alpha,12Beta,19Alpha)-

Brief Introduction

This product is a plant extract. It is used as a medical raw material and has the effect of reducing blood pressure. Used for content determination / identification / pharmacological experiment, etc.

Octahydro-2H-1-Benzopyran-2-One

MSDS

CAS:4430-31-3

Molecular Formula:C9H14O2

Alias

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Octahydrocoumarin; Bicyclononalactone; Octahydrochromen-2-One; Octahydro-2H-Chromen-2-One; Octahydro(2H)-1-Benzopyran-2-One; 2H-1-Benzopyran-2-One,Octahydro; Cyclohexyl Lactone; 1-Oxadecal-2-One; 3,4,4A,5,6,7,8,8A-Octahydrochromen-2-One; 2H-1-Benzopyran-2-One, Octahydro-

Brief Introduction

This product is a permitted edible spice and can be used as food additive.

[(2S)-1-(4-Amino-2-Oxopyrimidin-1-Yl)-3-Hydroxypropan-2-Yl]Oxymethyl-(3-Hexadecoxypropoxy)Phosphinic Acid

MSDS

CAS:444805-28-1

Molecular Formula:C27H52N3O7P

Alias

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Hdp-Cidofovir; 1-O-Hexadecylpropanediol-Cdv; Hdp-Hpmpc; Cmx001; Hdp-Cdv; Brincidofovir; Hexadecyloxypropyl-Cidofovir

Brief Introduction

Brincidofovir 是一种烷氧基烷基酯前药，含有合成的无环核苷单磷酸类似物西多福韦，通过其膦酸酯基团与脂质3-十六烷氧基-1-丙醇相连，对双链 DNA 病毒具有抗病毒活性。口服给药后，brincidofovir 穿过肠壁并穿透目标病毒感染细胞，然后被裂解为游离的抗病毒药物西多福韦。反过来，西多福韦被丙酮酸激酶磷酸化为其活性代谢物西多福韦二磷酸。西多福韦二磷酸与核苷酸结构相似，与脱氧胞嘧啶 5-三磷酸 ( dCTP )竞争病毒 DNA 聚合酶，并整合到不断增长的病毒 DNA 链中。因此，它可以防止 DNA 进一步聚合并破坏病毒的 DNA 复制。与静脉内给予的西多福韦相比，十六烷氧基丙基-西多福韦显示出更好的口服生物利用度、更低的毒性和增强的细胞渗透。

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