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20

Compounds

Cat No. Product Name Synonyms Targets
T81589 OVA-A2 Peptide SAINFEKL, OVA (257-264) Variant
OVA-A2 Peptide (SAINFEKL, OVA (257-264) Variant) is a biologically active, antigenic variant of the ovalbumin-derived peptide spanning amino acids 257 to 264.
T83852 EGFRvIII Peptide TFA PEGFRvIII (9-mer),Epidermal Growth Factor Receptor Variant III Peptide
EGFRvIII peptide, a synthetic peptide mirroring the EGFRvIII fusion junction—a tumor-specific, perpetually active EGFR variant missing amino acids 6-273 of the wild-type—binds to HLA-A*0201-positive T2 cells under MHC cl...
T7904 SR 19881 Estrogen/progestogen Receptor
SR 19881 is a full agonist of ERRγ(EC50 value of 0.39 μM in a binding assay and an EC50 value of 4.7 μM in a cell-based assay).
T9716 Ensitrelvir S-217622 SARS-CoV
Ensitrelvir (S-217622) is an orally active inhibitor of SARS-CoV-2 3CL protease with IC50 of 13 nM.
T8083 Pyridoxal 5'-​phosphate monohydrate Pyridoxal phosphate monohydrate,Pyridoxal 5-phosphate monohydrate Others
Pyridoxal 5'-phosphate monohydrate is an active vitamin B6 metabolite
T7905 PBD-150 Beta Amyloid
PBD-150 is an inhibitor of human glutaminyl cyclase (hQC) Y115E-Y117E variant( ki : 490 nM)
T64221 Linvencorvir RG7907 HBV , Antibiotic
Linvencorvir is a hepatitis B virus (HBV) core protein variant modifier used to treat chronic HBV infection.
T40279 GLP-1R modulator L7-028 GLP-1R modulator L7-028 cAMP , Glucagon Receptor
GLP-1R modulator L7-028 is a variant modulator that enhances affinity for GLP-1 and cAMP signaling.
T77407 Ensituximab NPC-1C,NEO-102,NEO-101
Ensituximab (NEO-102) is a quasi-selective IgG1 monoclonal antibody against the MUC5AC variant with anti-tumour activity that inhibits colorectal and pancreatic cancer.
T4220 BQR-695 BQR695,NVP-BQR695 PI3K , Parasite , PI4K
BQR-695 (NVP-BQR695) is a phosphatidylinositol 4-kinase (PI4K) inhibitor with IC50s of 80 and 3.5 nM for human PI4KIIIβ and Plasmodium variant of PI4KIIIβ, respectively.
T11421 Glutaminase-IN-1 CB839 derivative transporter
Glutaminase-IN-1 (CB839 derivative), a novel 1,3,4-selenodiazepine renal-type glutaminase (KGA) variant inhibitor, showed antitumor activity in an aggressive H22 hepatocellular carcinoma xenograft model.
T61191 EAI001 EGFR
EAI001 is a potent and selective mutant epidermal growth factor receptor (EGFR) variant inhibitor that inhibits EGFRL858R/T790M with an IC50 value of 24 nM.EAI001 can be used in cancer research.
T1952 MK-2206 dihydrochloride MK-2206 2HCl Apoptosis , Akt , Autophagy
MK-2206 dihydrochloride (MK-2206 2HCl) is a variant Akt inhibitor that inhibits Akt1, Akt2, and Akt3 (IC50=8/12/65 nM) with orally active, highly potent and selective potency. MK-2206 dihydrochloride exhibits antitumor a...
T64387 2-Nitrobenzoic acid o-Nitrobenzoic acid Others
2-Nitrobenzoic acid (o-Nitrobenzoic acid) is a antiproliferation agent. 2-Nitrobenzoic acid shows IC50 of 8.3 μM to jurkat cell line expressing T type calcium channel alpha 1H or its splice variant delta 25.
T26863 BMS-929075 BMS 929075,BMS929075 HCV Protease
BMS-929075 is an orally active HCV NS5B replicase (HCV NS5B replicase) palm site variant inhibitor with potency, high oral bioavailability and pharmacokinetic parameters.BMS-929075 shows cytotoxicity.
T82236 HBED-CC-tris(tert-butyl ester) Others
HBED-CC-tris(tert-butyl ester) is a monovalent variant of HBED-CC that can be used in the synthesis of synthetic radiocompounds based on asymmetric HBED-CC that can be used for tumor imaging.
T4757 L-Homoserine (S)-(-)-2-AMINO-4-HYDROXYBUTYRIC ACID Others , Endogenous Metabolite
L-Homoserine ((S)-(-)-2-AMINO-4-HYDROXYBUTYRIC ACID) is a more reactive variant of the amino acid serine. In this variant, the hydroxyl side chain contains an additional CH2 group which brings the hydroxyl group closer t...
TP1591L OVA G4 peptide acetate(148274-82-2 free base) SIIGFEKL acetate Others
OVA G4 peptide acetate(148274-82-2 free base) (SIIGFEKL acetate) is a variant of the agonist ovalbumin (OVA) peptide (257-264), SIINFEKL. OVA Peptide is a class I (Kb)-restricted peptide epitope of ovalbumin presented by...
T60835 SKF83959 Dopamine Receptor
SKF83959, a benzazepine analog, is a selective and potent partial agonist of the dopamine D1 receptor with Ki values of 1.18, 7.56, 920, and 399 nM for rat D1, D5, D2, and D3 receptors, respectively.SKF83959 is a potent ...
T10534 BI-4020 EGFR
BI-4020 is a fourth-generation, orally active, and non-covalent inhibitor of EGFR tyrosine kinase. BI-4020 exhibits activity agains the triple mutant EGFR del19 T790M C797S variant (IC50=0.2 nM in BaF3 cell lines), the d...
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