3D model is for representation purpose only.
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GCAGL | Palmitic acid |
Identification | |
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ConjuPepDB ID | cpd01574 |
Smiles | |
Inchi Key | InChIKey=BEMDCPUESIINHD-UHFFFAOYSA-N |
Molecular weight | 797.497 |
Molecular formula | C40H71N5O9S |
Chemical name | Peptide information |
Sequence (one letter) | GCAGL |
Length | 5 |
Peptide name | N/A |
External ID | |
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CAS number | 236424-94-5 |
Other information | |
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Application | Synthesis |
Additional function | Possible applications for the synthesis of functionalized lipidated peptides carrying e.g. fuorescent labels or biotin units |
Pharmacological class | other |
Conjugate type | tioester |
Linker | no |
Small molecule | Palmitic acid |
Small molecule CAS | 57-10-3 |
Small molecule structure | |
Structure method | 1H- and 13C NMR |
NMR solvent | CDCl3 |
Calculated properties | |
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LogP | 6.13012 |
Rotatable bonds | 34 |
H bond donor | 5 |
H bond acceptor | 7 |
Polar surface area (PSA) | 198.10000 |
Citations | |||||
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ID | Title | Year | Authors | Journal | DOI |
Synthesis of the palmitoylated and prenylated C-terminal lipopeptides of the human R- and N-Ras proteins | 1999 | Schmittberger, T.; Waldmann, H. | Bioorganic & Medicinal Chemistry |