AZD-7986
CAS No. 1802148-05-5
AZD-7986( INS-1007 | AZD 7986 | INS 1007 )
Catalog No. M12750 CAS No. 1802148-05-5
AZD-7986(INS-1007, AZD7986) is a highly potent, reversible, and selective DPP1 inhibitor with enzyme and cell pIC50 of 8.4.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 147 | In Stock |
|
| 10MG | 259 | In Stock |
|
| 25MG | 437 | In Stock |
|
| 50MG | 624 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
| 1 mL x 10 mM in DMSO | 128 | In Stock |
|
| 5MG | 117 | In Stock |
|
| 10MG | 188 | In Stock |
|
| 25MG | 377 | In Stock |
|
| 50MG | 535 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameAZD-7986
-
NoteResearch use only, not for human use.
-
Brief DescriptionAZD-7986(INS-1007, AZD7986) is a highly potent, reversible, and selective DPP1 inhibitor with enzyme and cell pIC50 of 8.4.
-
DescriptionAZD-7986(INS-1007, AZD7986) is a highly potent, reversible, and selective DPP1 inhibitor with enzyme and cell pIC50 of 8.4; shows excellent selectivity over other cathepsins, including cathepsins S, L, B, K, D, E, Z, H, and G; inhibits activation of all three NSPs (NE, Pr3, and CatG) with pIC50 of 7 in human primary bone marrow-derived CD34+ neutrophil progenitor cells; exhibits suitable human PK properties and is a clinical candidate for COPD.COPD Phase 1 Clinical.
-
In Vitro——
-
In Vivo——
-
SynonymsINS-1007 | AZD 7986 | INS 1007
-
PathwayMetabolic Enzyme/Protease
-
TargetDPP
-
RecptorDPP
-
Research AreaInflammation/Immunology
-
IndicationCOPD
Chemical Information
-
CAS Number1802148-05-5
-
Formula Weight420.469
-
Molecular FormulaC23H24N4O4
-
Purity>98% (HPLC)
-
SolubilityDMSO : ≥ 100 mg/mL 237.83 mM; H2O : < 0.1 mg/mL
-
SMILESN#C[C@H](CC1=CC=C(C2=CC=C(OC(N3C)=O)C3=C2)C=C1)NC([C@H]4OCCCNC4)=O
-
Chemical Name(S)-N-((S)-1-cyano-2-(4-(3-methyl-2-oxo-2,3-dihydrobenzo[d]oxazol-5-yl)phenyl)ethyl)-1,4-oxazepane-2-carboxamide
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Doyle K, et al. J Med Chem. 2016 Oct 27;59(20):9457-9472.
molnova catalog
related products
-
NU1025
NU1025 is a potent PARP inhibitor with IC50 of 400 nM.
-
Diprotin A
Diprotin A (Ile-Pro-Ile) is an inhibitor of dipeptidyl peptidase IV (DPP-IV).
-
3-Pyridylacetic acid...
It is an organic compunds with molecular fomula C7H8ClNO2.
Cart
sales@molnova.com