864953-29-7,MFCD23098796
Catalog No.:AA00GTZ5

864953-29-7 | BMS 663068

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
95%
1 week  
$127.00   $89.00
- +
2mg
95%
1 week  
$180.00   $126.00
- +
5mg
95%
1 week  
$243.00   $170.00
- +
10mg
95%
1 week  
$316.00   $221.00
- +
25mg
95%
1 week  
$511.00   $358.00
- +
50mg
95%
1 week  
$734.00   $514.00
- +
100mg
95%
1 week  
$1,026.00   $718.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00GTZ5
Chemical Name:
BMS 663068
CAS Number:
864953-29-7
Molecular Formula:
C25H26N7O8P
Molecular Weight:
583.4898
MDL Number:
MFCD23098796
SMILES:
COc1cnc(c2c1c(cn2COP(=O)(O)O)C(=O)C(=O)N1CCN(CC1)C(=O)c1ccccc1)n1cnc(n1)C
Properties
Computed Properties
 
Complexity:
1020  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
41  
Hydrogen Bond Acceptor Count:
11  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
8  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-0.1  

Downstream Synthesis Route

[1]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-US2005/209246,2005,A1Locationinpatent:Page/Pagecolumn46-48;54

864953-29-7   
CASUnavailable 

[1]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-US2005/209246,2005,A1Locationinpatent:Page/Pagecolumn36;37

[1]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-US2005/209246,2005,A1Locationinpatent:Page/Pagecolumn46;48;54;55

[2]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-US2005/209246,2005,A1Locationinpatent:Page/Pagecolumn35;36;37;39

[1]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-US2007/155702,2007,A1Locationinpatent:Page/Pagecolumn12

[1]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-US2007/155702,2007,A1Locationinpatent:Page/Pagecolumn12

Literature

Title: Pharmacodynamics, safety, and pharmacokinetics of BMS-663068, an oral HIV-1 attachment inhibitor in HIV-1-infected subjects.

Journal: The Journal of infectious diseases 20121001

Title: Nowicka-Sans B, et al. In vitro antiviral characteristics of HIV-1 attachment inhibitor BMS-626529, the active component of the prodrug BMS-663068. Antimicrob Agents Chemother. 2012 Jul;56(7):3498-507.

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Related Products of 864953-29-7
Tags:864953-29-7 Molecular Formula|864953-29-7 MDL|864953-29-7 SMILES|864953-29-7 BMS 663068
Catalog No.: AA00GTZ5
864953-29-7,MFCD23098796
864953-29-7 | BMS 663068
Pack Size: 1mg
Purity: 95%
1 week
$127.00 $89.00
Pack Size: 2mg
Purity: 95%
1 week
$180.00 $126.00
Pack Size: 5mg
Purity: 95%
1 week
$243.00 $170.00
Pack Size: 10mg
Purity: 95%
1 week
$316.00 $221.00
Pack Size: 25mg
Purity: 95%
1 week
$511.00 $358.00
Pack Size: 50mg
Purity: 95%
1 week
$734.00 $514.00
Pack Size: 100mg
Purity: 95%
1 week
$1,026.00 $718.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00GTZ5
Chemical Name: BMS 663068
CAS Number: 864953-29-7
Molecular Formula: C25H26N7O8P
Molecular Weight: 583.4898
MDL Number: MFCD23098796
SMILES: COc1cnc(c2c1c(cn2COP(=O)(O)O)C(=O)C(=O)N1CCN(CC1)C(=O)c1ccccc1)n1cnc(n1)C
Properties
Complexity: 1020  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 41  
Hydrogen Bond Acceptor Count: 11  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 8  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: -0.1  
Downstream Synthesis Route
864953-29-7    77-86-1    864953-39-9 

[1]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-US2005/209246,2005,A1Locationinpatent:Page/Pagecolumn46-48;54

864953-29-7   
CASUnavailable 

[1]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-US2005/209246,2005,A1Locationinpatent:Page/Pagecolumn36;37

864953-38-8    864953-29-7 

[1]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-US2005/209246,2005,A1Locationinpatent:Page/Pagecolumn46;48;54;55

[2]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-US2005/209246,2005,A1Locationinpatent:Page/Pagecolumn35;36;37;39

864953-29-7    77-86-1    864953-39-9 

[1]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-US2007/155702,2007,A1Locationinpatent:Page/Pagecolumn12

864953-29-7    942117-71-7 

[1]CurrentPatentAssignee:GLAXOSMITHKLINEPLC-US2007/155702,2007,A1Locationinpatent:Page/Pagecolumn12

Literature fold

Title: Pharmacodynamics, safety, and pharmacokinetics of BMS-663068, an oral HIV-1 attachment inhibitor in HIV-1-infected subjects.

Journal: The Journal of infectious diseases20121001

Title: Nowicka-Sans B, et al. In vitro antiviral characteristics of HIV-1 attachment inhibitor BMS-626529, the active component of the prodrug BMS-663068. Antimicrob Agents Chemother. 2012 Jul;56(7):3498-507.

Building Blocks More >
891494-64-7
891494-64-7
(S)-6-Bromo-3-(1-methyl-1h-pyrazol-4-yl)-5-(piperidin-3-yl)pyrazolo[1,5-a]pyrimidin-7-amine
AA00GU3O | MFCD23135226
90389-71-2
90389-71-2
N-(3-Nitrobenzyl)ethanamine hydrochloride
AA00GU86 | MFCD07110182
875159-65-2
875159-65-2
(2E)-3-[5-(2-METHYLCYCLOPROPYL)-2-FURYL]ACRYLIC ACID
AA00GUB7 | MFCD07838448
936630-57-8
936630-57-8
(R)-3-Amino-4-(2,4,5-trifluorophenyl)butyric acid
AA00GUFN | MFCD07363507
878465-67-9
878465-67-9
4-(Chloromethyl)-N-(4-methoxyphenyl)benzamide
AA00GUPX | MFCD08245261
914349-67-0
914349-67-0
4-(4-Ethylpiperazin-1-ylmethyl)benzylamine
AA00GUZ1 | MFCD06797801
92259-86-4
92259-86-4
Indolin-1-amine, HCl
AA00GVBD | MFCD04037889
915922-13-3
915922-13-3
N-[(1-methyl-1H-imidazol-2-yl)methyl]propan-1-amine
AA00GVG4 | MFCD08691582
915707-61-8
915707-61-8
3-[(6-Methylpyrazin-2-yl)oxy]aniline
AA00GVKJ | MFCD09702406
877802-01-2
877802-01-2
2-[(4-Chloro-1,2,5-thiadiazol-3-yl)(methyl)amino]ethanol
AA00GVP9 | MFCD05668093
Submit
© 2017 AA BLOCKS, INC. All rights reserved.