ProForma 2.0
validated simple linear
GLLHLLHHLLHHNH
LH12
Aliases: LH12
Normalized sequence
GLLHLLHHLLHHNH
14 amino acids
Release PepDiana-V1-20260620
43
Activity records
1
Source papers
36
Positive
7
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
1690.9506 Da
Molecular formula
C78H119N27O16
Theoretical pI
7.2059
Net charge at pH 7
0.2831
GRAVY
-0.0214
Instability index
26.2
Aromaticity
0
Topological polar surface area
656.79 Ų
cLogP
-2.7211
Hydrogen-bond donors
22
Hydrogen-bond acceptors
22
Rotatable bonds
53
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
GLLHLLHHLLHHNH
HELM 2.0
validated simple linear
PEPTIDE1{G.L.L.H.L.L.H.H.L.L.H.H.N.H}$$$$V2.0
Canonical SMILES
validated
CC(C)CC(NC(=O)CN)C(=O)NC(CC(C)C)C(=O)NC(Cc1c[nH]cn1)C(=O)NC(CC(C)C)C(=O)NC(CC(C)C)C(=O)NC(Cc1c[nH]cn1)C(=O)NC(Cc1c[nH]cn1)C(=O)NC(CC(C)C)C(=O)NC(CC(C)C)C(=O)NC(Cc1c[nH]cn1)C(=O)NC(Cc1c[nH]cn1)C(=O)NC(CC(N)=O)C(=O)NC(Cc1c[nH]cn1)C(=O)O
Isomeric SMILES
validated
CC(C)C[C@H](NC(=O)CN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)O
Paper-level observations
LH12 displayed stronger antibacterial activity against S. mutans at pH 5.5 with MICs ranging from 12.00 μg/mL to 64.00 μg/mL. Figure 2d.
LH12 displayed stronger antibacterial activity against S. mutans at pH 5.5 with MBCs ranging from 12.00 μg/mL to 64.00 μg/mL. Figure 2d.
MICs at pH 7.2 ranging from 21.33 μg/mL to more than 128.00 μg/mL. Figure 2d.
MBCs at pH 7.2 ranging from 21.33 μg/mL to more than 128.00 μg/mL. Figure 2d.
LH12 displayed stronger antibacterial activity against E. coli at pH 5.5 with MICs ranging from 12.00 μg/mL to 64.00 μg/mL. Figure 2d.
LH12 displayed stronger antibacterial activity against E. coli at pH 5.5 with MBCs ranging from 12.00 μg/mL to 64.00 μg/mL. Figure 2d.
MICs at pH 7.2 ranging from 21.33 μg/mL to more than 128.00 μg/mL. Figure 2d.
MBCs at pH 7.2 ranging from 21.33 μg/mL to more than 128.00 μg/mL. Figure 2d.
LH12 displayed stronger antibacterial activity against S. aureus at pH 5.5 with MICs ranging from 12.00 μg/mL to 64.00 μg/mL. Figure 2d.
LH12 displayed stronger antibacterial activity against S. aureus at pH 5.5 with MBCs ranging from 12.00 μg/mL to 64.00 μg/mL. Figure 2d.
MICs at pH 7.2 ranging from 21.33 μg/mL to more than 128.00 μg/mL. Figure 2d.
MBCs at pH 7.2 ranging from 21.33 μg/mL to more than 128.00 μg/mL. Figure 2d.
The MICs of LH12 against S. mutans were from 8.00 μg/mL to 16.00 μg/mL. Figure 4a.
The MBCs were from 16.00 μg/mL to 32.00 μg/mL. Figure 4a.
The MICs of LH12 against A. viscosus were from 8.00 μg/mL to 16.00 μg/mL. Figure 4a.
The MBCs were from 16.00 μg/mL to 32.00 μg/mL. Figure 4a.
The MICs of LH12 against A. naeslundii were from 8.00 μg/mL to 16.00 μg/mL. Figure 4a.
The MBCs were from 16.00 μg/mL to 32.00 μg/mL. Figure 4a.
The MICs of LH12 against L. casei were from 8.00 μg/mL to 16.00 μg/mL. Figure 4a.
The MBCs were from 16.00 μg/mL to 32.00 μg/mL. Figure 4a.
The MICs of LH12 against L. fermentum were from 8.00 μg/mL to 16.00 μg/mL. Figure 4a.
The MBCs were from 16.00 μg/mL to 32.00 μg/mL. Figure 4a.
The MIC of LH12 against S. salivarius was 48.00 μg/mL. Figure 4a.
The MBC was 64.00 μg/mL. Figure 4a.
The MICs and MBCs of LH12 against S. sanguinis were no less than 128.00 μg/mL. Figure 4a.
The MICs and MBCs of LH12 against S. sanguinis were no less than 128.00 μg/mL. Figure 4a.
The MICs and MBCs of LH12 against S. gordonii were no less than 128.00 μg/mL. Figure 4a.
The MICs and MBCs of LH12 against S. gordonii were no less than 128.00 μg/mL. Figure 4a.
The MICs and MBCs of LH12 against S. mitis were no less than 128.00 μg/mL. Figure 4a.
The MICs and MBCs of LH12 against S. mitis were no less than 128.00 μg/mL. Figure 4a.
8 μg/mL LH12 could reduce 84.04% of biofilm mass. Figure 6a.
16 μg/mL and 32 μg/mL LH12 totally inhibited the biofilm formation. Figure 6a.
32 μg/mL LH12 reduced the viable S. mutans in the preformed biofilms. Figure 6e.
32 μg/mL LH12 reduced the biofilm thickness to a half of that in the control group. Figure 6f.
16 μg/mL and 32 μg/mL LH12 could decrease the lactic acid production of the preformed biofilms. Figure 6c.
16 μg/mL and 32 μg/mL LH12 could decrease the water-insoluble EPS synthesis of the preformed biofilms. Figure 6d.
LH12 could inhibit the formation of the dual-species biofilm. Figure 7a.
LH12 could reduce its strength to make it easier to remove. Figure 7b.
The short-term treatment of LH12 reduced the lactic acid production of the dual-species biofilm. Figure 7d.
The short-term treatment of LH12 reduced the water-insoluble EPS synthesis of the dual-species biofilm. Figure 7e.
Only at a high concentration of 128 μg/mL would LH12 show slight cytotoxicity on HGECs with an inhibition ratio around 9.64% but without a significant reduction of the OD450 value after 45 min treatment. Figure 3a.
LH12 showed no hemolytic toxicity below 64 μg/mL and exhibited an increase of hemolysis ratio to 17.15% at 128 μg/mL. Figure 3c.
LH12 showed no hemolytic toxicity below 64 μg/mL. Figure 3c.
Citation and release provenance
Cite this identity as PepDiana record PEPDIA-PLP-001008, release PepDiana-V1-20260620. Experimental observations retain their paper, mention, and activity-record identifiers.
Record updated: 2026-06-22T07:14:26.229247+00:00