H-18, Hymenochirin-1B [P5K,E6K,D9K; A18,A22 S5]
General Information
DRACP ID DRACP02896
Peptide Name H-18, Hymenochirin-1B [P5K,E6K,D9K; A18,A22 S5]
Sequence IKLSKKTKKNLKKVLKGⓍIKGⓍIAVAKMV
Sequence Length 29
UniProt ID W8PRC4
PubChem CID Not available
Origin Synthetic (Derived from Hymenochirin-1B)
Type Synthetic peptide
Classification
Active ACP Stapled Peptides
Activity Information
Cell Line | Disease | Cancer Classified | Activity | Assay | Testing Time | Literature |
---|---|---|---|---|---|---|
A549 | Lung adenocarcinoma | Carcinoma | IC50=0.89±0.21 μM | MTT assay | 96 h | 1 |
HCT 116 | Colon carcinoma | Carcinoma | IC50=1.11±0.21 μM | MTT assay | 96 h | 1 |
HepG2 | Hepatoblastoma | Blastoma | IC50=1.61±0.21 μM | MTT assay | 96 h | 1 |
Hemolytic Activity Not available
Normal (non-cancerous) Cytotoxicity Not available
Target Not available
Affinity Not available
Mechanism Not available
Nature Anticancer
Structure Information
Helicity Not available
Linear/Cyclic Linear
Disulfide/Other Bond Stapled: Ⓧ(18) and Ⓧ (22) are cross-linked by hydrocarbon stapling
N-terminal Modification Free
C-terminal Modification Free
Other Modification Ⓧ=(S)-N-Fmoc-2-(4′-pentenyl)alanine
Chiral L
Physicochemical Information
Formula C137H254N38O29S
Absent amino acids CDEFHPQRWY
Common amino acids K
Mass 364945
Pl 11.75
Basic residues 10
Acidic residues 0
Hydrophobic residues 11
Net charge 10
Boman Index -1862
Hydrophobicity -6.21
Aliphatic Index 117.59
Half Life
/
Extinction Coefficient cystines 0
Absorbance 280nm 0
Polar residues 5
Amino acid distribution
Literature Information
Literature 1
Pubmed ID 30789695
Title Improving Selectivity, Proteolytic Stability, and Antitumor Activity of Hymenochirin-1B: A Novel Glycosylated Staple Strategy
Doi 10.1021/acschembio.9b00046
Year 2019
Patent
Patent ID Not available
Patent Title Not available
Other Iinformation Not available
Other Published ID Not available
External Code
DBAASP ID DBAASPS_18018