Primary information |
---|
ID | antitb_1195, |
Name | 24915878 |
N-Terminal modification | Boropentapeptide |
C-Terminal Modification | AVKAA-B(OH)2 |
Chemical Modification | Free |
Linear/Cyclic | Conjugated with Boronic acid |
Length | Conjugated with Boronic acid |
Chirality | Linear |
Nature | 5 |
Source | L |
Species | Synthetic |
Inhibition Concentration | Mycobacterium thermoresistible |
In Vitro/ In vivo | Mycobacterium thermoresistible |
Cell Line | Poorer inhibition than Pinanediol PD-protected Boropentapeptide |
Inhibition Concentration | In vitro |
Sequence | 2014 |
Cytotoxicity | None |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | None |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Inhibit enzyme (MycP1) reponsible for cleavage of virulence factor (ESX secretion-associated protein B (EspB)) |
Other activities | Mycosin protease-1 (MycP1) |
PMID | None |
Year of Publication | None |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1196, |
Name | 24915878 |
N-Terminal modification | Boropentapeptide |
C-Terminal Modification | AVKAA-B(OH)2 |
Chemical Modification | Free |
Linear/Cyclic | Conjugated with Boronic acid |
Length | Conjugated with Boronic acid |
Chirality | Linear |
Nature | 5 |
Source | L |
Species | Synthetic |
Inhibition Concentration | Mycobacterium smegmatis |
In Vitro/ In vivo | Mycobacterium smegmatis |
Cell Line | Poorer inhibition than Pinanediol PD-protected Boropentapeptide |
Inhibition Concentration | In vitro |
Sequence | 2014 |
Cytotoxicity | None |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | None |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Inhibit enzyme (MycP1) reponsible for cleavage of virulence factor (ESX secretion-associated protein B (EspB)) |
Other activities | Mycosin protease-1 (MycP1) |
PMID | None |
Year of Publication | None |
Tertiary Structure (Technique) | Not Predicted), |
Primary information |
---|
ID | antitb_1197, |
Name | 24915878 |
N-Terminal modification | Boropentapeptide |
C-Terminal Modification | AVKAA-B(OH)2 |
Chemical Modification | Free |
Linear/Cyclic | Conjugated with Boronic acid |
Length | Conjugated with Boronic acid |
Chirality | Linear |
Nature | 5 |
Source | L |
Species | Synthetic |
Inhibition Concentration | Mycobacterium tuberculosis |
In Vitro/ In vivo | Mycobacterium tuberculosis |
Cell Line | Poorer inhibition than Pinanediol PD-protected Boropentapeptide |
Inhibition Concentration | In vitro |
Sequence | 2014 |
Cytotoxicity | None |
In vivo Model | NA |
Lethal Dose | NA |
Immune Responce | None |
Mechanism of Action | NA |
Target | NA |
Combination Therapy | Inhibit enzyme (MycP1) reponsible for cleavage of virulence factor (ESX secretion-associated protein B (EspB)) |
Other activities | Mycosin protease-1 (MycP1) |
PMID | None |
Year of Publication | None |
Tertiary Structure (Technique) | Not Predicted), |