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. 2023 Dec 16;12(12):1534. doi: 10.3390/biology12121534

Table 1.

HN and HN analogues with neuroprotective/cytoprotective action.

Code Name Primary Structure Evaluation in
In Vitro/In Vivo Experimental Models
Ref.
HN MAPRGFSCLLLLTSEIDLPVKRRA +/+ [1,2,3]
HNG MAPRGFSCLLLLTGEIDLPVKRRA +/+ [1,2,3]
HN-D-Ser14 MAPRGFSCLLLLTsEIDLPVKRRA +/− [21]
HNGF6A MAPRGASCLLLLTGEIDLPVKRRA +/− [26]
AGA-(C8R)HNG17 PAGASRLLLLTGEIDLP +/+ [23]
CL SALLRSIPAPAGASRLLLLTGEIDLP +/+ [23]
des-Leu-CL SALLRSIPAPAGASRLLL_TGEIDLP −/+ [30]
tHN-C3 Hph-1 &-KKRLGLPGDEVDMAPRGFSCLLLLTSEIDLPVKRRA +/+ [34]
HUJInin YNAPVSIPQPAGASRLLLLTGEIDLP +/− [35]
c[D-Ser14-HN] c *(MAPAGASRLLLLTsEIDLPVKRRA) +/− [35]
HNSS R(d)-Dmt #-KFGG-MAPRGFSCLLLLTGEIDLPVKRRA +/+ [36]

* c: cyclic; # Dtm: 2′,6′-dimethyl tyrosine; & Hph-1: human transcription factor containing protein transduction domain (PTD)/cell penetrating peptide (CPP) sequences. All amino acid sequences are presented following the one-letter code. The amino acids that differ between parent HN and each HN analogue appear in red color and bold. Amino acid sequences that are irrelevant to HN appear with a gray background. According to the references shown in the table, HN/HN analogues have been evaluated in in vitro (+/−) or in in vivo (−/+) experimental models, or in both (+/+); moreover, all HN analogues have been prepared with peptide synthesis, except for HNSS which is reported as “commercially available” and tHN-C3, which has been prepared with molecular biology techniques as a fusion peptide.