Table 2.
Name | Description | Sequence | Target | Inhibitory activity (IC50) | Clinical status | Ref |
---|---|---|---|---|---|---|
SBP1 | A peptide derived from ACE-PD α1 helix | IEEQAKTFLDKFNHEAEDLFYQS | RBD | – | Preclinical | 280 |
AHB1 |
Derived from ACE2 Deep sequencing identified three ACE2 helix scaffolded designs |
DEDLEELERLYRKAEEVAKEAKDASRRGDDERAKEQMERAMRLFDQVFELAQELQEKQTDGNRQKATHLDKAVKEAADELYQRVRELEEQVMHVLDQVSELAHELLHKLTGEELERAAYFNWWATEMMLELIKSDDEREIREIEEEARRILEHLEELARK | RBD | LV: IC50 = 35 nM | Preclinical | 281 |
AHB2 | A truncate of AHB2 | ELEEQVMHVLDQVSELAHELLHKLTGEELERAAYFNWWATEMMLELIKSDDEREIREIEEEARRILEHLEELARK | RBD | LV: IC50 = 15.5 nM | Preclinical | 281 |
LCB1 | De novo interface designs | DKEWILQKIYEIMRLLDELGHAEASMRVSDLIYEFMKKGDERLLEEAERLLEEVER | RBD | LV: IC50 = 23.54 pM | Preclinical | 281 |
LCB3 | De novo interface designs | NDDELHMLMTDLVYEALHFAKDEEIKKRVFQLFELADKAYKNNDRQKLEKVVEELKELLERLLS | RBD | LV: IC50 = 48.1 pM | Preclinical | 281 |
IPB02 | A lipopeptide made by adding a cholesterol group to the C-terminal of IBP01 | ISGINASVVNIQKEIDRLNEVAKNLNESLIDLQELK (Chol) | S2-HR1 | PsV: IC50 = 0.08 μM | Preclinical | 293 |
EK1 | Derived from HR2 (OC43) | SLDQINVTFLDLEYEMKKLEEAIKKLEESYIDLKEL | S2-HR1 | PsV: IC50 = 2.375 μM | Preclinical | 289 |
LV: IC50 = 2.468 nM | ||||||
EK1C4 | cholesterol group to the C-terminal of EK1 | SLDQINVTFLDLEYEMKKLEEAIKKLEESYIDLKELGSGSG-PEG4 (Chol) | S2-HR1 | PsV: IC50 = 15.8 nM | Preclinical | 289 |
LV: IC50 = 36.5 nM | ||||||
2019-nCoV-HR2P | HR2 (1150–1185) | DISGINASVVNIQKEIDRLNEVAKNLNESLIDLQEL (aa1168–1203) | S2-HR1 | PsV: IC50 = 0.98 μM | Preclinical | 200 |
PsV pseudovirus, LV live virus