A peptide substrate for ATR
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RAD17-derived Peptide (trifluoroacetate salt)

Item No. 37512

Technical Information
Formal Name
L-alanyl-L-seryl-L-α-glutamyl-L-leucyl-L-prolyl-L-alanyl-L-seryl-L-glutaminyl-L-prolyl-L-glutaminyl-L-prolyl-L-phenylalanyl-L-seryl-L-alanyl-L-lysyl-L-lysyl-L-Lysine, trifluoroacetate salt
Molecular Formula
C81H132N22O25 • XCF3COOH
Formula Weight
Purity
≥98%
A solid
Peptide Sequence
ASELPASQPQPFSAKKK-OH
Water: soluble
SMILES
[H]N[C@H](C(N[C@@H](CO)C(N[C@@H](CCC(O)=O)C(N[C@@H](CC(C)C)C(N1CCC[C@H]1C(N[C@H](C(N[C@@H](CO)C(N[C@@H](CCC(N)=O)C(N2CCC[C@H]2C(N[C@@H](CCC(N)=O)C(N3CCC[C@H]3C(N[C@H](C(N[C@@H](CO)C(N[C@H](C(N[C@@H](CCCCN)C(N[C@@H](CCCCN)C(N[C@@H](CCCCN)C(O)=O)=O)=O)=O)C)=O)=O)CC4=CC=CC=C4)=O)=O)=O)=O)=O)=O)C)=O)=O)=O)=O)=O)C.OC(C(F)(F)F)=O
InChi Code
InChI=1S/C81H132N22O25.C2HF3O2/c1-43(2)38-55(97-70(116)50(28-31-64(109)110)92-73(119)57(41-105)98-65(111)44(3)85)80(126)103-37-15-23-59(103)75(121)89-46(5)67(113)99-58(42-106)74(120)93-51(26-29-62(86)107)78(124)101-35-16-24-60(101)76(122)94-52(27-30-63(87)108)79(125)102-36-17-25-61(102)77(123)96-54(39-47-18-7-6-8-19-47)71(117)100-56(40-104)72(118)88-45(4)66(112)90-48(20-9-12-32-82)68(114)91-49(21-10-13-33-83)69(115)95-53(81(127)128)22-11-14-34-84;3-2(4,5)1(6)7/h6-8,18-19,43-46,48-61,104-106H,9-17,20-42,82-85H2,1-5H3,(H2,86,107)(H2,87,108)(H,88,118)(H,89,121)(H,90,112)(H,91,114)(H,92,119)(H,93,120)(H,94,122)(H,95,115)(H,96,123)(H,97,116)(H,98,111)(H,99,113)(H,100,117)(H,109,110)(H,127,128);(H,6,7)/t44-,45-,46-,48-,49-,50-,51-,52-,53-,54-,55-,56-,57-,58-,59-,60-,61-;/m0./s1
InChi Key
NSLRAWXNLOWIRU-XXOXUGOMSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    RAD17-derived peptide is a peptide substrate for ataxia-telangiectasia and RAD3-related protein/kinase (ATR).1 It has been used to identify inhibitors of ATR.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Charrier, J.-D., Durrant, S.J., Golec, J.M.C., et alDiscovery of potent and selective inhibitors of ataxia telangiectasia mutated and Rad3 related (ATR) protein kinase as potential anticancer agents. J. Med. Chem. 54(7), 2320-2330 (2011).