

N-[2-(5-Chloro-1H-indol-3-yl)ethyl]-4-cyanobiphenyl-2-carboxaMide
CAS No. 1383373-65-6
N-[2-(5-Chloro-1H-indol-3-yl)ethyl]-4-cyanobiphenyl-2-carboxaMide( —— )
Catalog No. M35310 CAS No. 1383373-65-6
N-[2-(5-Chloro-1H-indol-3-yl)ethyl]-4'-cyanobiphenyl-2-carboxaMide, a TAU cytotoxicity inhibitor, inhibits LDH leakage of M17-TAU P301L cells with EC50 of 325nM.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 178 | Get Quote |
![]() ![]() |
5MG | 255 | Get Quote |
![]() ![]() |
10MG | 375 | Get Quote |
![]() ![]() |
25MG | 545 | Get Quote |
![]() ![]() |
50MG | 762 | Get Quote |
![]() ![]() |
100MG | 1017 | Get Quote |
![]() ![]() |
200MG | 1377 | Get Quote |
![]() ![]() |
500MG | Get Quote | Get Quote |
![]() ![]() |
1G | Get Quote | Get Quote |
![]() ![]() |
Biological Information
-
Product NameN-[2-(5-Chloro-1H-indol-3-yl)ethyl]-4-cyanobiphenyl-2-carboxaMide
-
NoteResearch use only, not for human use.
-
Brief DescriptionN-[2-(5-Chloro-1H-indol-3-yl)ethyl]-4'-cyanobiphenyl-2-carboxaMide, a TAU cytotoxicity inhibitor, inhibits LDH leakage of M17-TAU P301L cells with EC50 of 325nM.
-
DescriptionTAU-IN-1 (compound 051) is a TAU protein inhibitor with an EC50 value of 325 nM. TAU-IN-1 can be used in the study of neurodegenerative diseases.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorMicrotubule Associated
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1383373-65-6
-
Formula Weight399.87
-
Molecular FormulaC24H18ClN3O
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESC(CNC(=O)C1=C(C=CC=C1)C2=CC=C(C#N)C=C2)C=3C=4C(NC3)=CC=C(Cl)C4
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Gerard Griffioen et al. Novel compounds for the treatment of neurodegenerative diseases. WO2012080220A1.2012-06-21.
molnova catalog



related products
-
OAC3
OAC3 is an activator of octamer-bound transcription factor 4.
-
N-Aminofluorescein
N-Aminofluorescein is a highly selective and sensitive fluorescent probe for Cu2+ and can be used to detect Cu2+ in biological systems (λex/em=495/516 nm).
-
KRM-III
KRM-III is an orally active T cell antigen receptor (TCR) inhibitor with anti-inflammatory activity that potently inhibits TCR and myristate acetate/fosfomycin/ionomycin-induced NFAT nuclear factor activation and T cell proliferation, with an IC50 of approximately 5 μM.