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1051375-10-0,MFCD25976748
Catalog No.:AA008TDU

1051375-10-0 | Cabotegravir

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
98%
in stock  
$34.00   $24.00
- +
250mg
98%
in stock  
$60.00   $42.00
- +
1g
98%
in stock  
$149.00   $104.00
- +
5g
95%
in stock  
$710.00   $497.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA008TDU
Chemical Name:
Cabotegravir
CAS Number:
1051375-10-0
Molecular Formula:
C19H17F2N3O5
Molecular Weight:
405.3522
MDL Number:
MFCD25976748
SMILES:
Fc1ccc(c(c1)F)CNC(=O)c1cn2C[C@H]3OC[C@@H](N3C(=O)c2c(c1=O)O)C
Properties
Computed Properties
 
Complexity:
814  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
2  
Heavy Atom Count:
29  
Hydrogen Bond Acceptor Count:
8  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
3  
XLogP3:
2.1  

Downstream Synthesis Route

[1]CurrentPatentAssignee:SHIONOGI&CO.,LTD.;GLAXOSMITHKLINEPLC-WO2010/68262,2010,A1Locationinpatent:Page/Pagecolumn26-27

[2]CurrentPatentAssignee:SHIONOGI&CO.,LTD.;GLAXOSMITHKLINEPLC-US9133216,2015,B2Locationinpatent:Page/Pagecolumn17;18;21

[3]CurrentPatentAssignee:GLAXOSMITHKLINEPLC;SHIONOGI&CO.,LTD.-JP5848595,2016,B2Locationinpatent:Paragraph0045

[4]Johns,BrianA.;Kawasuji,Takashi;Weatherhead,JasonG.;Taishi,Teruhiko;Temelkoff,DavidP.;Yoshida,Hiroshi;Akiyama,Toshiyuki;Taoda,Yoshiyuki;Murai,Hitoshi;Kiyama,Ryuichi;Fuji,Masahiro;Tanimoto,Norihiko;Jeffrey,Jerry;Foster,ScottA.;Yoshinaga,Tomokazu;Seki,Takahiro;Kobayashi,Masanori;Sato,Akihiko;Johnson,MatthewN.;Garvey,EdwardP.;Fujiwara,Tamio[JournalofMedicinalChemistry,2013,vol.56,#14,p.5901-5916]

1051375-10-0   
CASUnavailable 

[1]CurrentPatentAssignee:LUPINLIMITED-US2021/9606,2021,A1Locationinpatent:Paragraph0102-0104

[2]Johns,BrianA.;Kawasuji,Takashi;Weatherhead,JasonG.;Taishi,Teruhiko;Temelkoff,DavidP.;Yoshida,Hiroshi;Akiyama,Toshiyuki;Taoda,Yoshiyuki;Murai,Hitoshi;Kiyama,Ryuichi;Fuji,Masahiro;Tanimoto,Norihiko;Jeffrey,Jerry;Foster,ScottA.;Yoshinaga,Tomokazu;Seki,Takahiro;Kobayashi,Masanori;Sato,Akihiko;Johnson,MatthewN.;Garvey,EdwardP.;Fujiwara,Tamio[JournalofMedicinalChemistry,2013,vol.56,#14,p.5901-5916]

[3]CurrentPatentAssignee:CIPLALTD-WO2019/159199,2019,A1Locationinpatent:Page/Pagecolumn40

[4]CurrentPatentAssignee:SHIONOGI&CO.,LTD.;GLAXOSMITHKLINEPLC-WO2010/68262,2010,A1Locationinpatent:Page/Pagecolumn27

[5]CurrentPatentAssignee:SHIONOGI&CO.,LTD.;GLAXOSMITHKLINEPLC-US9133216,2015,B2Locationinpatent:Page/Pagecolumn18;21;22

[6]CurrentPatentAssignee:GLAXOSMITHKLINEPLC;SHIONOGI&CO.,LTD.-JP5848595,2016,B2Locationinpatent:Paragraph0045

[7]CurrentPatentAssignee:KINGLAWRENCE;CIPLALTD-WO2015/177537,2015,A1Locationinpatent:Page/Pagecolumn40

[8]CurrentPatentAssignee:CIPLALTD-WO2018/109786,2018,A1Locationinpatent:Page/Pagecolumn42-44

[9]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-WO2018/149608,2018,A1Locationinpatent:Page/Pagecolumn38-39;40

[1]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-WO2011/119566,2011,A1

[2]CurrentPatentAssignee:ZUNYIMEDICALUNIVERSITY-CN114605437,2022,A

[1]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-WO2011/119566,2011,A1

[2]Wang,Huan;Kowalski,MatthewD.;Lakdawala,AmiS.;Vogt,FrederickG.;Wu,Lianming[OrganicLetters,2015,vol.17,#3,p.564-567]

[3]Wang,Huan;Kowalski,MatthewD.;Lakdawala,AmiS.;Vogt,FrederickG.;Wu,Lianming[OrganicLetters,2015,vol.17,#3,p.564-567]

[4]Wang,Huan;Kowalski,MatthewD.;Lakdawala,AmiS.;Vogt,FrederickG.;Wu,Lianming[OrganicLetters,2015,vol.17,#3,p.564-567]

[5]Wang,Huan;Kowalski,MatthewD.;Lakdawala,AmiS.;Vogt,FrederickG.;Wu,Lianming[OrganicLetters,2015,vol.17,#3,p.564-567]

[6]Wang,Huan;Kowalski,MatthewD.;Lakdawala,AmiS.;Vogt,FrederickG.;Wu,Lianming[OrganicLetters,2015,vol.17,#3,p.564-567]

[7]Wang,Huan;Kowalski,MatthewD.;Lakdawala,AmiS.;Vogt,FrederickG.;Wu,Lianming[OrganicLetters,2015,vol.17,#3,p.564-567]

[8]CurrentPatentAssignee:ZUNYIMEDICALUNIVERSITY-CN114605437,2022,A

1335210-23-5   
(3S,11aR)-N-(2,4-difluorophenyl)methyl-6-hydroxy-3-methyl-5,7-dioxo-2,3,5,7,11,11a-hexahydro1,3oxazolo3,2-apyrido1,2-dpyrazine-8-carboxamide 

[1]Patent:WO2011/119566,2011,A1

[2]OrganicLetters,2015,vol.17,p.564-567

[3]OrganicLetters,2015,vol.17,p.564-567

[4]OrganicLetters,2015,vol.17,p.564-567

[5]OrganicLetters,2015,vol.17,p.564-567

[6]OrganicLetters,2015,vol.17,p.564-567

[7]OrganicLetters,2015,vol.17,p.564-567

[8]Patent:WO2019/159199,2019,A1

Literature

Title: Antiviral Activity of Bictegravir and Cabotegravir against Integrase Inhibitor-Resistant SIVmac239 and HIV-1.

Journal: Antimicrobial agents and chemotherapy 20171201

Title: Impact of HIV-1 Integrase L74F and V75I Mutations in a Clinical Isolate on Resistance to Second-Generation Integrase Strand Transfer Inhibitors.

Journal: Antimicrobial agents and chemotherapy 20170801

Title: Antiviral characteristics of GSK1265744, an HIV integrase inhibitor dosed orally or by long-acting injection.

Journal: Antimicrobial agents and chemotherapy 20150101

Title: Zhou T, et al. Creation of a nanoformulated cabotegravir prodrug with improved antiretroviral profiles. Biomaterials. 2018 Jan;151:53-65.

Title: Reese MJ, et al. Drug interaction profile of the HIV integrase inhibitor cabotegravir: assessment from in vitro studies and a clinical investigation with midazolam. Xenobiotica. 2015 Sep 4:1-12.

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