936890-98-1,MFCD20275101
Catalog No.:AA00GU2E

936890-98-1 | OSI-027

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
98%
in stock  
$29.00   $20.00
- +
5mg
98%
in stock  
$73.00   $51.00
- +
10mg
98%
in stock  
$108.00   $76.00
- +
50mg
98%
in stock  
$294.00   $206.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00GU2E
Chemical Name:
OSI-027
CAS Number:
936890-98-1
Molecular Formula:
C21H22N6O3
Molecular Weight:
406.4378
MDL Number:
MFCD20275101
SMILES:
COc1cccc2=C/C(=c\3/nc(n4c3c(N)nc[nH]4)C3CCC(CC3)C(=O)O)/N=c12
Properties
Computed Properties
 
Complexity:
630  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
30  
Hydrogen Bond Acceptor Count:
7  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0  
Rotatable Bond Count:
4  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
2  

Downstream Synthesis Route

[1]CurrentPatentAssignee:ASTELLASPHARMAINC-WO2011/5909,2011,A2

[1]CurrentPatentAssignee:ASTELLASPHARMAINC-WO2011/5909,2011,A2Locationinpatent:Page/Pagecolumn14-15

[1]CurrentPatentAssignee:ASTELLASPHARMAINC-WO2011/5909,2011,A2

[1]CurrentPatentAssignee:ASTELLASPHARMAINC-WO2011/5909,2011,A2

Literature

Title: Discovery of 9-(6-aminopyridin-3-yl)-1-(3-(trifluoromethyl)phenyl)benzo[h][1,6]naphthyridin-2(1H)-one (Torin2) as a potent, selective, and orally available mammalian target of rapamycin (mTOR) inhibitor for treatment of cancer.

Journal: Journal of medicinal chemistry 20110310

Title: Falcon BL, et al. Reduced VEGF production, angiogenesis, and vascular regrowth contribute to the antitumor properties of dual mTORC1/mTORC2 inhibitors. Cancer Res. 2011 Mar 1;71(5):1573-83.

Title: Mateo J, et al. A first in man, dose-finding study of the mTORC1/mTORC2 inhibitor OSI-027 in patients with advanced solid malignancies. Br J Cancer. 2016;114(8):889-896.

Title: Zhang Y, et al. PP2AC Level Determines Differential Programming of p38-TSC-mTOR Signaling and Therapeutic Response to p38-Targeted Therapy in Colorectal Cancer. EBioMedicine. 2015 Nov 19;2(12):1944-56.

Title: Zhi X, et al. OSI-027 modulates acute graft-versus-host disease after liver transplantation in a rat model. Liver Transpl. 2017 Sep;23(9):1186-1198.

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Related Products of 936890-98-1
Tags:936890-98-1 Molecular Formula|936890-98-1 MDL|936890-98-1 SMILES|936890-98-1 OSI-027
Catalog No.: AA00GU2E
936890-98-1,MFCD20275101
936890-98-1 | OSI-027
Pack Size: 1mg
Purity: 98%
in stock
$29.00 $20.00
Pack Size: 5mg
Purity: 98%
in stock
$73.00 $51.00
Pack Size: 10mg
Purity: 98%
in stock
$108.00 $76.00
Pack Size: 50mg
Purity: 98%
in stock
$294.00 $206.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00GU2E
Chemical Name: OSI-027
CAS Number: 936890-98-1
Molecular Formula: C21H22N6O3
Molecular Weight: 406.4378
MDL Number: MFCD20275101
SMILES: COc1cccc2=C/C(=c\3/nc(n4c3c(N)nc[nH]4)C3CCC(CC3)C(=O)O)/N=c12
Properties
Complexity: 630  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 30  
Hydrogen Bond Acceptor Count: 7  
Hydrogen Bond Donor Count: 3  
Isotope Atom Count: 0  
Rotatable Bond Count: 4  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 2  
Downstream Synthesis Route
103-49-1    936890-98-1 

[1]CurrentPatentAssignee:ASTELLASPHARMAINC-WO2011/5909,2011,A2

936890-98-1    77-86-1    1187559-63-2 

[1]CurrentPatentAssignee:ASTELLASPHARMAINC-WO2011/5909,2011,A2Locationinpatent:Page/Pagecolumn14-15

936902-01-1    936890-98-1 

[1]CurrentPatentAssignee:ASTELLASPHARMAINC-WO2011/5909,2011,A2

936902-00-0    936890-98-1 

[1]CurrentPatentAssignee:ASTELLASPHARMAINC-WO2011/5909,2011,A2

Literature fold

Title: Discovery of 9-(6-aminopyridin-3-yl)-1-(3-(trifluoromethyl)phenyl)benzo[h][1,6]naphthyridin-2(1H)-one (Torin2) as a potent, selective, and orally available mammalian target of rapamycin (mTOR) inhibitor for treatment of cancer.

Journal: Journal of medicinal chemistry20110310

Title: Falcon BL, et al. Reduced VEGF production, angiogenesis, and vascular regrowth contribute to the antitumor properties of dual mTORC1/mTORC2 inhibitors. Cancer Res. 2011 Mar 1;71(5):1573-83.

Title: Mateo J, et al. A first in man, dose-finding study of the mTORC1/mTORC2 inhibitor OSI-027 in patients with advanced solid malignancies. Br J Cancer. 2016;114(8):889-896.

Title: Zhang Y, et al. PP2AC Level Determines Differential Programming of p38-TSC-mTOR Signaling and Therapeutic Response to p38-Targeted Therapy in Colorectal Cancer. EBioMedicine. 2015 Nov 19;2(12):1944-56.

Title: Zhi X, et al. OSI-027 modulates acute graft-versus-host disease after liver transplantation in a rat model. Liver Transpl. 2017 Sep;23(9):1186-1198.

Building Blocks More >
917111-44-5
917111-44-5
CYT997
AA00GU5Z | MFCD18206787
923190-13-0
923190-13-0
N-[2-[4-(AMINOSULFONYL)PHENYL]ETHYL]-2-CHLOROPROPANAMIDE
AA00GUA8 | MFCD08444166
877041-39-9
877041-39-9
2-CHLORO-N-[4-(4-METHOXYPHENYL)-4-METHYL-2,5-DIOXOIMIDAZOLIDIN-1-YL]ACETAMIDE
AA00GUDU | MFCD07843129
916792-17-1
916792-17-1
2-Bromo-4-fluoro-5-methylbenzaldehyde
AA00GULR | MFCD07782045
879442-52-1
879442-52-1
3-(5-Methyl-2-furyl)-1h-pyrazole-5-carboxylic acid
AA00GUU2 | MFCD05170058
908117-93-1
908117-93-1
Fmoc-ABG-OH HCl
AA00GV6A | MFCD09752870
910442-16-9
910442-16-9
7-Chloro-3-methyl-1h-indole-2-carbaldehyde
AA00GVE6 | MFCD08361795
89585-53-5
89585-53-5
3-chloro-N-methyl-N-phenylpropanamide
AA00GVJ8 | MFCD02973802
91134-85-9
91134-85-9
2-Hydroxy-5-(morpholinosulfonyl)benzoic acid
AA00GVNG | MFCD00539987
889937-01-3
889937-01-3
1-[4-(Methylsulfonyl)phenyl]-1-propanamine
AA00GVRT | MFCD12827484
Submit
© 2017 AA BLOCKS, INC. All rights reserved.