ProForma 2.0
validated simple linear
CYGSR
C-CR5
Aliases: C-CR5, L-CR5
Normalized sequence
CYGSR
5 amino acids
Release PepDiana-V1-20260620
21
Activity records
1
Source papers
18
Positive
3
Negative / threshold
Versioned scientific descriptors
No separate physicochemical property was reported in the primary-literature identity record. PepDiana release values are shown as computed properties.
Molecular weight
584.6457 Da
Molecular formula
C23H36N8O8S
Theoretical pI
8.222
Net charge at pH 7
0.7492
GRAVY
-0.9
Instability index
29.54
Aromaticity
0.2
Topological polar surface area
282.08 Ų
cLogP
-3.8974
Hydrogen-bond donors
12
Hydrogen-bond acceptors
10
Rotatable bonds
17
Method: PepDiana sequence/structure descriptor pipeline
Tool: Biopython+RDKit · Biopython 1.85; RDKit 2024.09.6
Calculated: 2026-06-20T11:01:38.358971+00:00
Assumptions: ph=7; termini=free N-terminus and free C-terminus for simple linear peptides; stereochemistry=standard L-amino acids; smiles_length_limit=200
ProForma 2.0
validated simple linear
CYGSR
HELM 2.0
validated simple linear
PEPTIDE1{C.Y.G.S.R}$$$$V2.0
Canonical SMILES
validated
N=C(N)NCCCC(NC(=O)C(CO)NC(=O)CNC(=O)C(Cc1ccc(O)cc1)NC(=O)C(N)CS)C(=O)O
Isomeric SMILES
validated
N=C(N)NCCC[C@H](NC(=O)[C@H](CO)NC(=O)CNC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](N)CS)C(=O)O
Paper-level observations
The IC50 of L-CR5 was calculated as 377.83 ± 34.32 μg/mL (646.25 ± 58.70 μM). Figure 3 caption: IC50 = 377.83 ± 34.32 μg/mL; (646.25 ± 58.70 μM), n = 3.
the IC50 of C-CR5 was found to be 16.92 ± 0.47 μg/mL (29.86 ± 0.83 μM). Figure 3 caption: IC50 = 16.92 ± 0.47 μg/mL; (29.86 ± 0.83 μM), n = 3.
The scavenging ability of L-CR5 gradually increased from 18% to 53% in the range of 25–400 μg/mL.
The scavenging ability of L-CR5 gradually increased from 18% to 53% in the range of 25–400 μg/mL.
C-CR5 showed very high activity from 73% to 83% under the same concentration condition [25–400 μg/mL].
C-CR5 showed very high activity from 73% to 83% under the same concentration condition [25–400 μg/mL].
IC50 of L-CR5 was calculated as 377.83 ± 34.32 μg/mL (646.25 ± 58.70 μM).
IC50 of C-CR5 was found to be 16.92 ± 0.47 μg/mL (29.86 ± 0.83 μM).
The IC50 of L-CR5 was calculated as 680.63 ± 15.68 μg/mL (1164.0 ± 27.3 μM). Figure 4 caption: IC50 = 680.63 ± 15.68 μg/mL; (1164.0 ± 27.3 μM), n = 3.
the IC50 of C-CR5 was identified as 104.2 ± 5.3 μg/mL (184.0 ± 9.4 μM). Figure 4 caption: IC50 = 104.2 ± 5.3 μg/mL; (184.0 ± 9.4 μM), n = 3.
IC50 of L-CR5 was calculated as 680.63 ± 15.68 μg/mL (1164.0 ± 27.3 μM).
IC50 of C-CR5 was identified as 104.2 ± 5.3 μg/mL (184.0 ± 9.4 μM).
In the range of 50–800 μg/mL, the tyrosinase inhibitory rate of L-CR5 gradually increased from 1.16% to 57.35%.
In the range of 50–800 μg/mL, the tyrosinase inhibitory rate of L-CR5 gradually increased from 1.16% to 57.35%.
C-CR5 showed a rapid increase from 30.91% to 97.79% in the same concentration section [50–800 μg/mL].
C-CR5 showed a rapid increase from 30.91% to 97.79% in the same concentration section [50–800 μg/mL].
L-CR5 showed expression levels of 99–100% in the 25–100 μg/mL range, had little tendency to decrease, and no significant inhibitory effect was observed at 100.80% even at 200 and 400 μg/mL.
the expression level of C-CR5 decreased sharply from 200 μg/mL to 63.31%.
decreased to 7.78% at 400 μg/mL, showing almost complete inhibitory effects.
As a result of treating the RAW 264.7 macrophages with L-CR5 and C-CR5 at a concentration of 6.25–400 μg/mL, cell viability was maintained at 95% or more in all treatment groups.
As a result of treating the RAW 264.7 macrophages with L-CR5 and C-CR5 at a concentration of 6.25–400 μg/mL, cell viability was maintained at 95% or more in all treatment groups.
Citation and release provenance
Cite this identity as PepDiana record PEPDIA-PLP-000379, release PepDiana-V1-20260620. Experimental observations retain their paper, mention, and activity-record identifiers.
Record updated: 2026-06-22T07:14:26.229247+00:00