20
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T2355 | CFTR(inh)-172 | CFTRinh 172,CFTR Inhibitor-172,CFTRinh-172,CFTRinh172 | CFTR , Autophagy |
CFTR(inh)-172 (CFTR Inhibitor-172) is a voltage-independent, selective CFTR inhibitor. | |||
T35883 | RNF5 inhibitor inh-02 | RNF5 inhibitor inh-02 | |
RNF5 inhibitor inh-02, a potent E3 ubiquitin ligase RNF5/RMA1 inhibitor, demonstrates significant efficacy in rescuing F508del-CFTR with an EC50 of 2.2 uM in bronchial epithelial cells homozygous for the F508del mutation... | |||
T24846 | T16A(inh)-C01 | T16A(inh) C01 | |
T16A(inh)-C01 is the Ca(2+)-activated Cl(-) Channel, Ano1 class C inhibitor. | |||
T24847 | T16A(inh)-D01 | T16A(inh) D01,T16Ainh-D01,T16AinhD01,T16A(inh)D01,T16Ainh D01 | |
T16A(inh)-D01 is the Ca(2+)-activated Cl(-) Channel, Ano1 class D inhibitor. | |||
T24845 | T16A(inh)-B01 | T16Ainh-B01,T16A(inh)B01,T16AinhB01,T16Ainh B01 | |
T16A(inh)-B01 is the Ca(2+)-activated Cl(-) Channel, Ano1 class B inhibitor. | |||
T71615 | INH-13 | ||
INH-13 is a Aurora inhibitor. | |||
T0972 | Isoniazid | INH,Isonicotinic acid hydrazide,Isonicotinic hydrazide | Mitophagy , Dehydrogenase , CAT , Antibacterial , Autophagy |
Isoniazid (Isonicotinic hydrazide) is an antibacterial agent used primarily as a tuberculostatic. | |||
T6180 | INH6 | Apoptosis , Microtubule Associated | |
INH6, an effective Hec1 inhibitor, selectively disrupts the Hec1/Nek2 interaction and induces chromosome mis-alignment. | |||
T11657 | INH154 | Others | |
INH154 is a highly potent inhibitor for Nek2 and Hec1 binding (INH), with IC50s of 120 nM and 200 nM for INH in MB468 and Hela cells. | |||
T2502 | INH1 | IBT13131 | Apoptosis , Microtubule Associated |
INH1 (IBT13131) is a cell-permeable Hec1 inhibitor that specifically disrupts the Hec1/Nek2 interaction. | |||
T5209 | INH14 | IκB/IKK | |
INH14 is a novel inhibitor of the IKKα/β-dependent TLR inflammatory response (IC50s: 8.97/3.59 μM for IKKα/IKKβ). | |||
T29081 | UTA1inh-C1 | UTA1-inh-C1,UTA1(inh)-C1 | |
UTA1inh-C1 is a novel inhibitor of kidney urea transporter UT-A1. | |||
T29080 | UTA1inh-B1 | UTA1(inh)-B1,UTA1inhB1 | |
UTA1inh-B1 is a novel inhibitor of kidney urea transporter UT-A1. | |||
T29079 | UTA1inh-A1 | UTA1-inh-A1,UTA1(inh)-A1 | |
UTA1inh-A1 is a novel inhibitor of kidney urea transporter UT-A1. | |||
T29082 | UTA1inh-D1 | UTA1-inh-D1,UTA1inh D1,UTA1(inh)-D1,UTA1inhD1 | |
UTA1inh-D1 is a novel inhibitor of kidney urea transporter UT-A1 . | |||
T81024 | Tefibazumab | INH-H 2002 | |
Tefibazumab, a humanized IgG1κ monoclonal antibody, targets and binds to clumping factor A, an adhesion protein expressed on the surface of Staphylococcus aureus, and is under investigation for the treatment of serious S... | |||
T71613 | MK-8712 | ||
MK-8712 is a monobactam beta-lactamase inhibitor. | |||
T2602 | Barasertib-HQPA | 1H-Pyrazole-3-acetamide,Barasertib,AZD1152-HQPA,AZD2811,AZD1152-HQPA|AZD2811 | Apoptosis , Aurora Kinase |
Barasertib-HQPA (AZD2811) is a highly selective Aurora B inhibitor (IC50: 0.37 nM) and demonstrates ~3,700-fold greater selectivity than Aurora A. | |||
T9845 | Thrombin inhibitor 5 | ||
Thrombin inhibitor 5 (compound 385) is a thrombin inhibitor with IC 50s ranging from 0.1 μM to 1 μM. Thrombin inhibitor 5 can be used for venous thromboembolism research[1]. | |||
T37422L | Ras Inhibitory Peptide acetate | Ras Inhibitory Peptide acetate(159088-48-9 Free base) | Ras |
Ras Inhibitory Peptide acetate is a peptide involved in the Ras-dependent signaling pathway that plays an important role in human cancers initiated by oncogenic receptors. |