H-2, Hymenochirin-1B [E6,N10 S5]
General Information
DRACP ID DRACP02889
Peptide Name H-2, Hymenochirin-1B [E6,N10 S5]
Sequence IKLSPⓍTKDⓍLKKVLKGAIKGAIAVAKMV
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=4.26±0.52 μM | MTT assay | 96 h | 1 |
HCT 116 | Colon carcinoma | Carcinoma | IC50=3.54±0.72 μM | MTT assay | 96 h | 1 |
HepG2 | Hepatoblastoma | Blastoma | IC50=1.60±0.24 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: Ⓧ(6) and Ⓧ (10) 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 C130H234N34O30S
Absent amino acids CEFHNQRWY
Common amino acids K
Mass 350520
Pl 11.2
Basic residues 7
Acidic residues 1
Hydrophobic residues 13
Net charge 6
Boman Index -43
Hydrophobicity 41.03
Aliphatic Index 124.48
Half Life
/
Extinction Coefficient cystines 0
Absorbance 280nm 0
Polar residues 4
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_18012