3D model is for representation purpose only.
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SRSELIVHQRLF | palmitic acid |
Identification | |
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ConjuPepDB ID | cpd00252 |
Smiles | |
Inchi Key | InChIKey=IBGLZWRIQUTORX-KZPBBPCKSA-N |
Molecular weight | 1733.06 |
Molecular formula | C80H136N26O17 |
Chemical name | Peptide information |
Sequence (one letter) | SRSELIVHQRLF |
Length | 12 |
Peptide name | antimicrobial peptide Cm-p5 |
External ID | |
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CAS number | 1781222-37-4 |
Other information | |
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Application | Synthesis, incorporation of complex N-substituents at both termini and at internal positions |
Additional function | Modifications of biologically relevant peptides: fluorescent labeling, PEGylation, glycosylation, etc. |
Pharmacological class | other |
Conjugate type | amine |
Linker | no |
Small molecule | palmitic acid |
Small molecule CAS | 57-10-3 |
Small molecule structure | |
Calculated properties | |
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LogP | -4.80088 |
Rotatable bonds | 64 |
H bond donor | 22 |
H bond acceptor | 28 |
Polar surface area (PSA) | 697.15000 |
Citations | |||||
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ID | Title | Year | Authors | Journal | DOI |
Aminocatalysis-Mediated on-Resin Ugi Reactions: Application in the Solid-Phase Synthesis of N-Substituted and Tetrazolo Lipopeptides and Peptidosteroids | 2015 | Morales, Fidel E.; Garay, Hilda E.; Munoz, Daniela F.; Augusto, Yarelys E.; Otero-Gonzalez, Anselmo J.; Reyes Acosta, Osvaldo; Rivera, Daniel G. | Organic Letters |