Cyclopropyl-ester-P1
General
Type : Fluorescent Probe, Cyclopropyl
Chemical_Nomenclature :
Canonical SMILES : N5(C(=CC=CC(=CC=CC1=[N+](C2=C(C1(C)C)C=CC=C2)CCCC[S](=O)(=O)[O-])C(=O)OCC3=CC=C(C=C3)OC(C4CC4)=O)C(C6=C5C=CC=C6)(C)C)CCCC[S](=O)(=O)O[Na]
InChI : InChI=1S\/C47H54N2O10S2.Na\/c1-46(2)38-17-5-7-19-40(38)48(29-9-11-31-60(52,53)54)42(46)21-13-15-35(44(50)58-33-34-23-27-37(28-24-34)59-45(51)36-25-26-36)16-14-22-43-47(3,4)39-18-6-8-20-41(39)49(43)30-10-12-32-61(55,56)57\;\/h5-8,13-24,27-28,36H,9-12,25-26,29-33H2,1-4H3,(H-,52,53,54,55,56,57)\;\/q\;+1\/p-1
InChIKey : LFNMOAIDBXRUGA-UHFFFAOYSA-M
Other name(s) :
Target
Structures : No structure
Families : BCHE, Carb_B_Chordata
References (1)
| Title : Fluorescent cyclopropyl ester probes are efficiently cleaved by endogenous carboxylesterase in mouse blood: implications for preclinical fluorescence imaging - Sanders_2023_Supramol.Chem_34_484 |
| Author(s) : Sanders HS , Atkinson KM , Smith BD |
| Ref : Supramol Chem , 34 :484 , 2023 |
| Abstract : |
| PubMedSearch : Sanders_2023_Supramol.Chem_34_484 |
| PubMedID: 40046405 |