18F-Psma 1007

18F-PSMA-1007 is a fluorine-18 labeled PSMA-targeting ligand combining a peptidomimetic binding motif with a radiolabeled prosthetic group. The structure is optimized for receptor affinity and metal-free radionuclide attachment. Researchers investigate its kinetics, binding constants, and metabolic stability in model systems. Applications include tracer-design studies, PSMA-epitope mapping, and radioligand-structure optimization.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.

CAT No: ta-586

Synonyms/Alias:18F-PSMA 1007; (2~{S})-2-[[(2~{S})-6-[[(2~{S})-2-[[4-[[[(2~{S})-2-[[(2~{S})-2-[(6-fluoranylpyridin-3-yl)carbonylamino]-5-oxidanyl-5-oxidanylidene-pentanoyl]amino]-5-oxidanyl-5-oxidanylidene-pentanoyl]amino]methyl]phenyl]carbonylamino]-3-naphthalen-2-yl-propanoyl]amino]-1-oxidanyl-1-oxidanylidene-hexan-2-yl]carbamoylamino]pentanedioic acid; 2093321-18-5; SCHEMBL20180889; F-PSMA 1007; PSMA-1007?; AT43725; 9OT

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M.F/Formula
C49H55FN8O16
M.W/Mr.
1031
InChI
InChI=1S/C49H55FN8O16/c50-38-18-14-32(26-52-38)43(66)54-34(16-20-40(61)62)46(69)55-33(15-19-39(59)60)44(67)53-25-27-8-12-30(13-9-27)42(65)56-37(24-28-10-11-29-5-1-2-6-31(29)23-28)45(68)51-22-4-3-7-35(47(70)71)57-49(74)58-36(48(72)73)17-21-41(63)64/h1-2,5-6,8-14,18,23,26,33-37H,3-4,7,15-17,19-22,24-25H2,(H,51,68)(H,53,67)(H,54,66)(H,55,69)(H,56,65)(H,59,60)(H,61,62)(H,63,64)(H,70,71)(H,72,73)(H2,57,58,74)/t33-,34-,35-,36-,37-/m0/s1
InChI Key
RFFFFGRYVZESLB-LTLCPEALSA-N

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