品牌咨询
联系方式
公司地址
苏州工业园区生物纳米园A4#216
联系电话
4000-520-616 / 18915418616
传真号码
0512-67156496
电子邮箱
info@ebiomall.com
公司网址
https://www.ebiomall.com

MedKoo Biosciences/PIK-39/406327/200mg

价格
面议
货号:406327-200mg
浏览量:30
品牌:MedKoo
服务
全国联保
正品保证
正规发票
签订合同
商品描述
PIK-39isapotentPI3Kinhibitor.

MedKooCat#:406327
Name:PIK-39
CAS#:371242-53-4
ChemicalFormula:C21H15ClN6O2S
ExactMass:450.06657
MolecularWeight:450.9
ElementalAnalysis:C,55.94;H,3.35;Cl,7.86;N,18.64;O,7.10;S,7.11


Synonym:PIK39;PIK39;PIK-39.

IUPAC/ChemicalName:2-(((9H-purin-6-yl)thio)methyl)-5-chloro-3-(2-methoxyphenyl)quinazolin-4(3H)-one

InChiKey:UMMYTDJYDSTEMB-UHFFFAOYSA-N

InChiCode:InChI=1S/C21H15ClN6O2S/c1-30-15-8-3-2-7-14(15)28-16(27-13-6-4-5-12(22)17(13)21(28)29)9-31-20-18-19(24-10-23-18)25-11-26-20/h2-8,10-11H,9H2,1H3,(H,23,24,25,26)

SMILESCode:O=C1N(C2=CC=CC=C2OC)C(CSC3=C4N=CNC4=NC=N3)=NC5=C1C(Cl)=CC=C5


TechnicalData

Appearance:
Solidpowder

Purity:
>98%(orrefertotheCertificateofAnalysis)

ShippingCondition:
Shippedunderambienttemperatureasnon-hazardouschemical.ThisproductisstableenoughforafewweeksduringordinaryshippingandtimespentinCustoms

StorageCondition:
0–4oCforshortterm(weeksto1month)or-20oCforlongterms(monthstoyears).

Solubility:
SolubleinDMSO,notsolubleinwater.

ShelfLife:
>2yearsifstoredproperly.

DrugFormulation:
ThisdrugmaybeformulatedinDMSO

StockSolutionStorage:
0-4Cforshortterm(daystoweeks),or-20Cforlongterm(months).

HarmonizedSystemCode:
293490


AdditionalInformation

  
 
 
 


References

1.Methodsfortreatingoncoviruspositivecancers.ByJimeno,Antonio;Hausman,DianaF.;Peterson,Scott.FromPCTInt.Appl.(2012),WO2012118978A120120907,2.Useofphosphatidylinositol-3'-kinase(PI3K)p110deltaisoforminhibitorsfortreatingretroviralinfectionandreplication.ByKatsikis,PeterD.;Boesteanu,AlinaC.;Turner,Martin.FromPCTInt.Appl.(2012),WO2012009452A120120119,

3.Geneticpolymorphismsasindicatorsfortheuseofphosphatidylinositol-3-kinasep110Δ-targeteddrugsinthetreatmentofpsychiatricdisorders.ByLaw,AmandaJ.;Weinberger,DanielR..FromPCTInt.Appl.(2010),WO2010065923A220100610,

4.Thep110δstructure:MechanismsforselectivityandpotencyofnewPI(3)Kinhibitors.[ErratumtodocumentcitedinCA152:375583].ByBerndt,Alex;Miller,Simon;Williams,Olusegun;Le,DanielD.;Houseman,BenjaminT.;Pacold,JosephI.;Gorrec,Fabrice;Hon,Wai-Ching;Ren,Pingda;Rommel,Christian;etal.FromNatureChemicalBIOLOGy(2010),6(4),306.,

5.Thep110δstructure:mechanismsforselectivityandpotencyofnewPI(3)Kinhibitors.[ErratumtodocumentcitedinCA152:375583].ByBerndt,Alex;Miller,Siimon;Williams,Olusegun;Le,DanielD.;Houseman,BenjaminT.;Pacold,JosephI.;Gorrec,Fabrice;Hon,Wai-Chon;Liu,Yi;Rommel,Christian;etal.FromNatureChemicalBiology(2010),6(3),244.,

6.Thep110δstructure:mechanismsforselectivityandpotencyofnewPI(3)Kinhibitors.ByBerndt,Alex;Miller,Simon;Williams,Olusegun;Le,DanielD.;Houseman,BenjaminT.;Pacold,JosephI.;Gorrec,Fabrice;Hon,Wai-Ching;Liu,Yi;Rommel,Christian;etal.FromNatureChemicalBiology(2010),6(2),117-124.,DOI:10.1038/nchembio.293

7.Phosphoinositide-3-kinase(PI3K)inhibitors:Identificationofnewscaffoldsusingvirtualscreening.ByFrederick,Raphael;Mawson,Claire;Kendall,JackieD.;Chaussade,Claire;Rewcastle,GordonW.;Shepherd,PeterR.;Denny,WilliamA..FromBioorganic&MedicinalChemistryLetters(2009),19(20),5842-5847.,DOI:10.1016/j.bmcl.2009.08.087

8.Phosphoinositidemodulationforthetreatmentofneurodegenerativediseases.ByKim,Tae-Wan;Dipaolo,Gilbert;Kang,MinSuk;Berman,Diego;McIntire,LauraBethJohnson.FromPCTInt.Appl.(2008),WO2008064244A220080529,

9.Methodsofinhibitingleukocyteaccumulation.ByDiacovo,ThomasG.;Hayflick,JoelS.;Puri,KamalD..FromPCTInt.Appl.(2006),WO2006089106A220060824,

10.ApharmacologicalmapofthePI3-Kfamilydefinesaroleforp110αininsulinsignaling.ByKnight,ZacharyA.;Gonzalez,Beatriz;Feldman,MorriE.;Zunder,EliR.;Goldenberg,DavidD.;Williams,Olusegun;Loewith,Robbie;Stokoe,David;Balla,Andras;Toth,Balazs;etal.FromCell(Cambridge,MA,UnitedStates)(2006),125(4),733-747.,DOI:10.1016/j.cell.2006.03.035

11.AdualPI3kinase/mTORinhibitorrevealsemergentefficacyinglioma.ByFan,Qi-Wen;Knight,ZacharyA.;Goldenberg,DavidD.;Yu,Wei;Mostov,KeithE.;Stokoe,David;Shokat,KevanM.;Weiss,WilliamA..FromCancerCell(2006),9(5),341-349.,DOI:10.1016/j.ccr.2006.03.029

12.Actionmechanismsandstructure-activityrelationshipsofPI3Kγinhibitorsontheenzyme:amolecularmodelingstudy.ByKuang,R.-R.;Qian,F.;Li,Z.;Wei,D.-Z.;Tang,Y..FromEuropeanJournalofMedicinalChemistry(2006),41(4),558-565.,DOI:10.1016/j.ejmech.2006.01.017

13.Methodsfortreatingmastcelldisorders.ByHayflick,JoelS.;Pefaur,Noah;Puri,KamalD.;Tino,William.FromPCTInt.Appl.(2005),WO2005120511A120051222,

14.Methodsusingphosphoinositide3-kinaseδinhibitorsfortreatingand/orpreventingaberrantproliferationofhematopoieticcells.ByHayflick,JoelS.;Bouscary,Didier;Lacombe,Catherine;Mayeux,Patrick.FromPCTInt.Appl.(2005),WO2005117889A120051215,

15.Phosphoinositide3-kinaseδselectiveinhibitorsforinhibitingangiogenesis.ByHallahan,Dennis;Hayflick,JoelS.;Sadhu,Chanchal.FromPCTInt.Appl.(2005),WO2005112935A120051201,

16.Phosphoinositide3-kinaseδ-selectiveinhibitorsfortreatingandpreventinghypertensionandhypertension-relateddisorders.ByWatts,StephanieW.;Northcott,CarrieA..FromPCTInt.Appl.(2005),WO2005067901A220050728,

17.MethodsofinhibitingimmuneresponsesstimulatedbyanendogenousfactorbyadmiNISTeringphosphoinositide3-kinaseδselectiveinhibitors.ByDouangpanya,Jason;Hayflick,JoelS.;Puri,KamalD..FromU.S.Pat.Appl.Publ.(2005),US20050043239A120050224,

18.Methodsofinhibitingleukocyteaccumulation.ByDiacovo,ThomasG.;Hayflick,JoelS.;Puri,KamalD..FromPCTInt.Appl.(2005),WO2005016349A120050224,

19.Methodusingaphosphoinositide3-kinaseδinhibitorforinhibitingimmuneresponsesstimulatedbyanendogenousfactor.ByDouangpanya,Jason;Hayflick,JoelS.;Puri,KamalD..FromPCTInt.Appl.(2005),WO2005016348A120050224,~6Citings

20.Preparationofpurinylquinazolinonesasinhibitorsofhumanphosphatidylinositol3-kinasedelta.BySadhu,Chanchal;Dick,Ken;Treiberg,Jennifer;Sowell,C.Gregory;Kesicki,EdwardA.;Oliver,Amy.FromU.S.Pat.Appl.Publ.(2002),US20020161014A120021031,

21.Quinazolinonederivativesasinhibitorsofhumanphosphatidylinositol3-kinasedelta.BySadhu,Chanchal;Dick,Ken;Treiberg,Jennifer;Sowell,C.Gregory;Kesicki,EdwardA.;Oliver,Amy.FromPCTInt.Appl.(2001),WO2001081346A220011101.

我国旅美科学家陈清奇博士创立的MedKoo美帝药库医药公司目前正在建立全球第一个小分子抗癌药库。 MedKoo是一家以研发、生产和销售小分子抗癌化合物为主的医药科技公司。 业务范围 为全球所有从事抗癌药物研究和开发的制药公司,高校,研究院所,政府相关机构提供与抗癌药物分子相关的产品、试剂和技术服务。 技术核心 以药物化学合成技术为核心,密切结合全球抗癌新药研发领域中的新技术、新理论、新趋势和新的发展方向,不断推出抗癌化合物新品种。 建造目标 MedKoo美帝药库的目标是:建成全球最大的小分子抗癌药库 ,品种最多最全、质量最好最可靠。美帝药库的宗旨是:客户第一;质量第一;信誉第一;创新第一。