DprE1-IN-1
CAS No. 1494675-86-3
DprE1-IN-1( TBA-7371 | TBA 7371 | TBA7371 )
Catalog No. M17323 CAS No. 1494675-86-3
DprE1-IN-1 is a potent inhibitor of DprE1 and PDE6.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 27 | In Stock |
|
| 5MG | 41 | In Stock |
|
| 10MG | 61 | In Stock |
|
| 25MG | 113 | In Stock |
|
| 50MG | 186 | In Stock |
|
| 100MG | 317 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameDprE1-IN-1
-
NoteResearch use only, not for human use.
-
Brief DescriptionDprE1-IN-1 is a potent inhibitor of DprE1 and PDE6.
-
DescriptionTBA-7371 is a non-covalent inhibitor of decaprenylphosphoryl-β-D-ribose 2’-epimerase (DprE1) with an IC50 value of 10 nM. It also inhibits PDE6 with an IC50 value of 4 μM.1 AZ 7371 has been shown to be active against M. tuberculosis with an MIC range of 0.78-3.12 μM and demonstrates efficacy in a rodent model of tuberculosis.
-
In Vitro——
-
In Vivo——
-
SynonymsTBA-7371 | TBA 7371 | TBA7371
-
PathwayAngiogenesis
-
TargetCDK
-
RecptorDprE1
-
Research AreaInfection|Inflammation/Immunology
-
Indication——
Chemical Information
-
CAS Number1494675-86-3
-
Formula Weight355.39
-
Molecular FormulaC18H21N5O3
-
Purity>98% (HPLC)
-
SolubilityDMSO : 11 mg/mL. 30.95 mM;
-
SMILESCc1cc2c(c(cn2Cc2c(c(ncn2)OC)C)C(=O)NCCO)nc1
-
Chemical NameN-(2-hydroxyethyl)-1-((6-methoxy-5-methylpyrimidin-4-yl)methyl)-6-methyl-1H-pyrrolo[3,2-b]pyridine-3-carboxamide
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Shirude PS, et al. J Med Chem. 2014 Jul 10;57(13):5728-37.
molnova catalog
related products
-
NVP-LCQ195
NVP-LCQ195 (AT9311) is a potent inhibitor of CDK1, CDK2, CDK3 and CDK5 (IC50: 1-42 nM).
-
Lerociclib dihydroch...
Lerociclib dihydrochloride is a potent and selective inhibitor of CDK4/CDK6, with IC50s of 2 nM and 1 nM for CDK6/CyclinD3?and CDK4/CyclinD1, respectively.?
-
Benzo[b]thiophene-2-...
Benzo[b]thiophene-2-sulfonamide, N-[3-(aminomethyl)phenyl]-5-chloro-3-methyl- directly inhibits InhA and does not require activation by the catalase peroxidase KatG.
Cart
sales@molnova.com