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1443460-91-0
  • names:

    GSK2838232

  • CAS號(hào):

    1443460-91-0

    MDL Number: No data available
  • MF(分子式): C48H73ClN2O6 MW(分子量): 809.56
  • EINECS:No data available Reaxys Number:No data available
  • Pubchem ID:71580991 Brand:BIOFOUNT
GSK2838232
GSK2838232(1443460-91-0)是抗艾滋病毒劑,用于治療艾滋病和/或制止艾滋病毒感染傳播的藥物。這些不包括用于治療與艾滋病相關(guān)的癥狀或機(jī)會(huì)性感染的藥物.通過(guò)高含量成像確定抗病毒活性是在10 uM時(shí)抑制SARS-CoV-2誘導(dǎo)的Caco-2細(xì)胞的細(xì)胞毒性,作用時(shí)間為10 uM。
 
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中文別名 GSK2838232(1443460-91-0),GSK-2838232;GSK2838232;GSK 2838232;4-[[((3aR,5aR,5bR,7aR,9S,11aR,11bR,13aS)-3a-[(1R)-2-[(4-氯苯基)甲基-[2-(二甲基氨基)乙基]氨基]- 1-羥乙基] -5a,5b,8,8,11a-五甲基-2-氧代-1-丙-2-基-4,5,6,7,7a,9,10,11,11b,12,13 ,13a-十二烷基-3H-環(huán)戊[a] chrysen-9-基]氧基] -2,2-dime;
英文別名 GSK2838232(1443460-91-0),4-[[(3aR,5aR,5bR,7aR,9S,11aR,11bR,13aS)-3a-[(1R)-2-[(4-chlorophenyl)methyl-[2-(dimethylamino)ethyl]amino]-1-hydroxyethyl]-5a,5b,8,8,11a-pentamethyl-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3H-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dime;
CAS號(hào) 1443460-91-0
Inchi InChI = 1S / C48H73ClN2O6 / c1-30(2)40-34(52)26-48(37(53)29-51(25-24-50(10)11)28-31-12-14-32( 49)15-13-31)23-22-46(8)33(41(40)48)16-17-36-45(7)20-19-38(57-39(54)27-43( 3,4)42(55)56)44(5,6)35(45)18-21-47(36,46)9 / h12-15,30,33,35-38,53H,16-29H2, 1-11H3,(H,55,56)/ t33-,35 +,36-,37 +,38 +,45 +,46-,47-,48 + / m1 / s1
InchiKey MEOWKUXNVNJAMY-PZFKGGKESA-N
分子式 Formula C48H73ClN2O6
分子量 Molecular Weight 809.56
溶解度Solubility 生物體外In Vitro:DMSO溶解度≥ 50 mg/mL(61.76 mM)*"≥" means soluble可溶, but saturation unknown溶解度未知.
性狀 白色至灰白色固體粉末,Power
儲(chǔ)藏條件 Storage conditions 存放在陰涼干燥處,短期(數(shù)天至數(shù)周)在0-4℃,長(zhǎng)期(數(shù)月至數(shù)年)在-56℃。保質(zhì)期2年。

GSK2838232(1443460-91-0)實(shí)驗(yàn)注意事項(xiàng):
1.實(shí)驗(yàn)前需戴好防護(hù)眼鏡,穿戴防護(hù)服和口罩,佩戴手套,避免與皮膚接觸。
2.實(shí)驗(yàn)過(guò)程中如遇到有毒或者刺激性物質(zhì)及有害物質(zhì)產(chǎn)生,必要時(shí)實(shí)驗(yàn)操作需要手套箱內(nèi)完成以免對(duì)實(shí)驗(yàn)人員造成傷害
3.實(shí)驗(yàn)后產(chǎn)生的廢棄物需分類(lèi)存儲(chǔ),并交于專(zhuān)業(yè)生物廢氣物處理公司處理,以免造成環(huán)境污染Experimental considerations:
1. Wear protective glasses, protective clothing and masks, gloves, and avoid contact with the skin during the experiment.
2. The waste generated after the experiment needs to be stored separately, and handed over to a professional biological waste gas treatment company to avoid environmental pollution.
Tags:GSK2838232試劑,GSK2838232雜質(zhì),GSK2838232中間體,GSK2838232密度,GSK2838232合成,GSK2838232密度,GSK2838232溶解度,GSK2838232旋光度,GSK2838232閃點(diǎn),GSK2838232購(gòu)買(mǎi),
產(chǎn)品說(shuō)明 (1443460-91-0)GSK2838232 GSK2838232是Betulin的衍生物,是一種新型的人類(lèi)免疫病毒(HIV)成熟抑制劑,正在開(kāi)發(fā)用于治療慢性HIV感染.
IntroductionGSK2838232(1443460-91-0)inhibit HIV reverse transcriptase activity across a broad panel of HIV isolates, extracted from patent WO/2013090664A1, compound51.
Application1
Application2
Application3
GSK2838232(1443460-91-0)藥理學(xué):
GSK2838232(1443460-91-0)是Betulin的衍生物,GSK2838232是一種新型的人類(lèi)免疫病毒(HIV)成熟抑制劑,正在開(kāi)發(fā)用于治療慢性HIV感染。GSK2838232是抗艾滋病毒劑,用于治療艾滋病和/或制止艾滋病毒感染傳播的藥物。這些不包括用于治療與艾滋病相關(guān)的癥狀或機(jī)會(huì)性感染的藥物.通過(guò)高含量成像確定抗病毒活性是在10 uM時(shí)抑制SARS-CoV-2誘導(dǎo)的Caco-2細(xì)胞的細(xì)胞毒性,作用時(shí)間為10 uM。
Hatcher Mark Andrew, et al. Preparation of betulin derivatives for the treatment of HIV. From PCT Int. Appl. (2013), WO 2013090664 A1 20130620.

GSK2838232(1443460-91-0)參考文獻(xiàn):
1、US2018042944    藥物成分    2017-10-19  
  This web page summarizes information in PubChem about patent US-2018042944-A1. This includes chemicals mentioned, as reported , as well as other content, such as title, abstract, and International Patent Classification (IPC) codes. To read more about how this page was constructed, please visit the PubChem patents help page. The present Invention relates to long acting pharmaceutical compositions of betulin derivatives or pharmaceutically acceptable salts thereof, useful in the treatment or prevention of Human Immunodeficiency Virus (HIV) infections.

2、US2017348324    樺木的衍生物    2017-08-24  
This web page summarizes information in PubChem about patent US-2017348324-A1. This includes chemicals mentioned, as reported by PubChem contributors, as well as other content, such as title, abstract, and International Patent Classification (IPC) codes. To read more about how this page was constructed,
The present invention relates to compounds characterized by having a structure according to the following Formula I: n n n n n n n n n n , or a pharmaceutically acceptable salt thereof. Compounds of the present invention are useful for the treatment or prevention of HIV.


3、US2017252356    用木犀草素衍生物治療HIV的化合物和組合物    2017-03-21  
This web page summarizes information in PubChem about patent US-2017252356-A1. This includes chemicals mentioned, as reported by PubChem contributors, as well as other content, such as title, abstract, and International Patent Classification (IPC) codes. To read more about how this page was constructed。
The present invention relates to compounds characterized by having a structure according to the following Formula I: n n n n n n n n n n or a pharmaceutically acceptable salt thereof. Compounds of the present invention are useful for the treatment or prevention of HIV. 

4、US2016120878    樺木的衍生物    2015-12-23    2016-05-05
This web page summarizes information in PubChem about patent US-2016120878-A1. This includes chemicals mentioned, as reported by PubChem contributors, as well as other content, such as title, abstract, and International Patent Classification (IPC) codes. To read more about how this page was constructed, 
The present invention relates to compounds characterized by having a structure according to the following formula I: n n n n n n n n n n n n or a pharmaceutically acceptable salt thereof. Compounds of the present invention are useful for the treatment or prevention of HIV.

5、US2014357643    樺木素衍生物    2014-08-18    2014-12-04
This web page summarizes information in PubChem about patent US-2014357643-A1. This includes chemicals mentioned, as reported by PubChem contributors, as well as other content, such as title, abstract, and International Patent Classification (IPC) codes. To read more about how this page was constructed,
The present invention relates to compounds characterized by having a structure according to the following Formula I: n n n n n n n n n n , or a pharmaceutically acceptable salt thereof. Compounds of the present invention are useful for the treatment or prevention of HIV.

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