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AOB11689
CAS: 2458219-65-1
Chemical Name: (2S,4R)-1-((R)-2-(9-(4-(4-((3-((3-Amino-5-(4-amino-4-methylpiperidin-1-yl)pyrazin-2-yl)thio)-2-chlorophenyl)amino)-4-oxobutanoyl)piperazin-1-yl)nonanamido)-3,3-dimethylbutanoyl)-4-hydroxy-N-((R)-1-(4-(4-methylthiazol-5-yl)phenyl)ethyl)pyrrolidine-2-carboxamide
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Quantity | mg | Unit Price ($/mg or $/Unit) | Final Price |
---|---|---|---|
1 | 100 | $76.05 | Total: $7,605.00 |
1 | 50 | $87.88 | Total: $4,394.00 |
1 | 25 | $103.09 | Total: $2,577.25 |
1 | 10 | $121.68 | Total: $1,216.80 |
1 | 5 | $143.65 | Total: $718.25 |
Molecular Formula | C30H27N3O15 |
Molecular Weight | 669.55 |
CAS Numbers | 28384-96-5 |
Storage Condition | 0°C (short term), -20°C (long term), desiccated |
Solubility | DMSO |
Purity | 98% by HPLC |
Synonym | SHP2-D26; SHP2 D26; SHP2D26 |
IUPAC/Chemical Name | (2S,4R)-1-((S)-2-(9-(4-(4-((3-((3-amino-5-(4-amino-4-methylpiperidin-1-yl)pyrazin-2-yl)thio)-2-chlorophenyl)amino)-4-oxobutanoyl)piperazin-1-yl)nonanamido)-3,3-dimethylbutanoyl)-4-hydroxy-N-((S)-1-(4-(4-methylthiazol-5-yl)phenyl)ethyl)pyrrolidine-2-carboxamide |
InChl Key | XJSPAQRZSJUBLB-WQFCSRJTSA-N |
InChl Code | InChI=1S/C56H79ClN12O6S2/c1-36(38-17-19-39(20-18-38)49-37(2)61-35-76-49)62-52(74)42-32-40(70)34-69(42)54(75)50(55(3,4)5)65-45(71)16-11-9-7-8-10-12-25-66-28-30-68(31-29-66)47(73)22-21-46(72)63-41-14-13-15-43(48(41)57)77-53-51(58)64-44(33-60-53)67-26-23-56(6,59)24-27-67/h13-15,17-20,33,35-36,40,42,50,70H,7-12,16,21-32,34,59H2,1-6H3,(H2,58,64)(H,62,74)(H,63,72)(H,65,71)/t36-,40+,42-,50+/m0/s1 |
SMILES Code | O=C([C@H]1N(C([C@H](C(C)(C)C)NC(CCCCCCCCN2CCN(C(CCC(NC3=CC=CC(SC4=NC=C(N5CCC(C)(N)CC5)N=C4N)=C3Cl)=O)=O)CC2)=O)=O)C[C@H](O)C1)N[C@@H](C)C6=CC=C(C7=C(C)N=CS7)C=C6 |
References | .1) Mingliang Wang, Jianfeng Lu, Mi Wang, Chao-Yie Yang, and Shaomeng Wang. Discovery of SHP2-D26 as a First, Potent, and Effective PROTAC Degrader of SHP2 Protein. Journal of Medicinal Chemistry Article ASAP. DOI: 10.1021/acs.jmedchem.0c00471 |
First, Potent, and Effective PROTAC Degrader of SHP2 Protein, being is >30-times more potent in inhibition of phosphorylation of extracellular signal-regulated kinase (ERK) and of cell growth than SHP099, a potent SHP2 inhibitor, in KYSE520 and MV4;11 cancer cell lines