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Cat No. | Product Name | Synonyms | Targets |
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T9359 | PDL-1 cpd 10 | PD-1/PD-L1 | |
PDL-1 cpd 10 is a novel small molecule PD-L1 inhititor. | |||
T9794 | cpd.5 of 2234271-86-2 | ||
cpd.5 of 2234271-86-2 is a useful organic compound for research related to life sciences. The catalog number is T9794 and the CAS number is 2234284-82-1. | |||
T13492 | 3,5-Diiodothyropropionic acid | C082182,Ditpa cpd | Thyroid hormone receptor(THR) |
3,5-Diiodothyropropionic acid (C082182) is a thyroid hormone analog. It induces α-myosin heavy chain mRNA expression, binds to thyroid hormone receptor (Ka: 2.40/M and 4.06/M for TRα1 and TRβ1). | |||
T3199 | PTACH | NCH-51,Cpd 51 | HIV Protease , HDAC |
PTACH (Cpd 51) (NCH-51) is a SAHA-based inhibitor of human HDAC. It can potently inhibit the growth of various human Y cells (EC50: 1 to 10 μM). | |||
T9547 | Cpd.4 | Others | |
Cpd.4 is a chemical agent. | |||
T9559 | Cpd.7 of 1326852-06-5 | ||
Cpd.7 of 1326852-06-5 is a useful organic compound for research related to life sciences. The catalog number is T9559 and the CAS number is 2411843-75-7. | |||
T12123L | Cpd.5 of 1207358-59-5 | ||
Cpd.5 of 1207358-59-5 is a useful organic compound for research related to life sciences. The catalog number is T12123L and the CAS number is 1207365-47-6. | |||
T8754 | CPD2028 | Others | |
CPD2028 is an intermediate of ND630, a potent acetyl coenzyme A carboxylase (ACC) inhibitor. | |||
T75140 | CPD-1224 | ||
CPD-1224, an orally active derivative that binds cereblon ligands to ALK inhibitors, specifically targets and degrades EML4-ALK oncogenic fusions, including ALK and its mutants L1196M/G1202R. | |||
T35349 | CU-CPD107 | CU-CPD107 | TLR |
CU-CPD107 is a selective agonist of toll-like receptor 8 (TLR8) and also shows activation activity against ssRNA ligands. CU-CPD107 acts as an inhibitor of TLR8 signaling in the presence of R848 (IC50=13.7 μM). CU-CPD10... | |||
T33372 | MF 13 | MF13Cpd,MF13 Cpd,MF-13,MF13,MF13-Cpd | |
MF 13 exhibits tumor apoptosis activity. | |||
T22298 | CPD3615-A5 | Others | |
CPD3615-A5 is an active chemical. | |||
T31949 | Glutathione amide | GASH cpd,L-gamma-Glutamyl-L-cysteinylglycinamide | |
Glutathione amide is a enzyme of a chimeric protein. | |||
T8688 | (Rac)-X77 | CPD77,MUN91789 | SARS-CoV |
(Rac)-X77 (MUN91789) is a potent SARS- CoV- 2 main protease inhibitor. | |||
T23686 | AHR-activator-1023 | Branching Morphogenesis Modulator 1023,Cpd 1023,Compound 1023,BMM 1023 | |
AHR-activator-1023 is the aryl hydrocarbon receptor activator. It is also a specific FGF2-induced branching morphogenesis modulator. | |||
T26936 | C188 | Cpd188,STAT3-IN-C188,Cpd-188,C 188,C-188 | |
C188 is a cell-permeable naphthol compound and a STAT3 inhibitor. C188 inhibits IL-6-stimulated STAT3 Tyr705 phosphorylation and nuclear translocation in HepG2 cells by targeting STAT3 SH2 domain peptide-binding pocket, ... | |||
T68310 | CPD7 | ||
CPD7 is a novel non-RBD binding modulator to inhibit SARS-CoV-2 by prohibiting the conformational change of the spike (S) protein. | |||
T69252 | CPD26 | ||
CPD26 is a novel non-RBD binding modulator to inhibit SARS-CoV-2 by prohibiting the conformational change of the spike (S) protein. | |||
T31864 | FPFS-1169 HCl | R-(-)-BPAP,FPFS 1169,FPFS-1169 hydrochloride,BPAP-cpd,R-FPFS-1169,FPFS1169 | |
FPFS-1169 (BPAP-CPD, R-(-)-BPAP, R- FpFS-1169) is a proto-oncogene protein C-Bcl-2 stimulant that is one of the "catecholaminergic and serotonergic enhancers" and may be used for the treatment of Parkinson's disease. | |||
T71363 | ACT-281959 | ||
ACT-281959, a prodrug of ACT-246475, is a novel potent and selective P2Y12 Receptor Antagonist with a Wider Therapeutic Window in the Rat Than Clopidogrel. ACT-281959 showed antithrombotic efficacy after oral administr... | |||
T71987 | 5-hydroxy Isatin | ||
5-hydroxy Isatin is an inhibitor of monoamine oxidase A and also inhibits atrial natriuretic peptide-induced activation of particulate guanylyl cyclase in rat brain and heart membranes. | |||
T69292 | IQDMA | ||
IQDMA is an inhibitor of the transcription factor STAT5. | |||
T9539 | (E)-1,7,7-trimethyl-3-((3-(trifluoromethyl)phenyl)imino)bicyclo【2.2.1】heptan-2-one | ||
(E)-1,7,7-trimethyl-3-((3-(trifluoromethyl)phenyl)imino)bicyclo【2.2.1】heptan-2-one is a useful organic compound for research related to life sciences and the catalog number is T9539. | |||
T10877 | CPDA | Phosphatase | |
CPDA is a new potent inhibitor of SH2 domain-containing inositol phosphatase 2 (SHIP2). | |||
T9807 | CPDS | Others | |
CPDS is a non permeant thiol agent which affects several mitochondrial functions. In rat liver mitochondria, CPDS inhibits only the Pi/OH- carrier; both CPDS and n-butylmalonate are necessary to inhibit completely Pi ent... | |||
T3484 | Trans-ACPD | Trans-(±)-ACP,1-amino-1,3-dicarboxycyclopentane,(±)-trans-ACPD | GluR |
trans-ACPD ((±)-trans-ACPD) is an equimolecular mixture of (1S, 3R)- and (1R, 3S)-ACPD. trans-ACPD is a selective agonist of the mGluR (metabotropic glutamate receptor); active at the group I/II mGlu receptors (EC50: 2/1... | |||
T22488 | (1S,3R)-ACPD | Others | |
(1S,3R)-ACPD is a group I and II mGlu receptor agonist. | |||
T23080 | NPEC-caged-(1S,3R)-ACPD | Others | |
NPEC-caged-(1S,3R)-ACPD is a group I and II mGlu receptor agonist. | |||
T71989 | CPD7 HCl | ||
CPD7 HCl is a novel non-RBD binding modulator to inhibit SARS-CoV-2 by prohibiting the conformational change of the spike (S) protein. | |||
T23897 | CLK1/2-IN-3 | CLK1/2 inhibitor 3,CLK1/2-inhibitor-3,CLK1/2 IN 3,CLK1/2IN3 | CDK |
CLK1/2-IN-3 (Cpd-3) is a potent and selective CLK1 and CLK2 inhibitor with antiproliferative activity and inhibits the activities of CLK1, CLK2, SRPK1, SRPK2, and SRPK3.CLK1/2-IN-3 induces nuclear speckle enlargement, wh... | |||
T10603 | BRD-6929 | HIV Protease , HDAC | |
BRD-6929 is a selective, brain-penetrant HDAC1 and HDAC2 inhibitor (IC50: 1 and 8 nM). BRD-6929 (Cpd-60) shows high-affinity to HDAC1 and HDAC2 (Kis: 0.2 and 1.5 nM) [2]. BRD-6929 potentiates the efficacy of gnidimacrin... | |||
T32376 | Kenazepine | ||
Kenazepine is a benzodiazepine cpd containing functional alkylating moiety. | |||
T34508 | Sanazole | AK2123,AK-2123,AK 2123 | |
Sanazole is a 3-nitrotriazole cpd. It can affect the human cervical cancer cell line. | |||
T25007 | AGLME | N-alpha-Acetylglycyllysyl methyl ester | |
AGLME is used in a direct enzymatic assay for activated Hageman factor measuring the ability of Hageman factor to hydrolyze the cpd. | |||
T28320 | PD 121373 | PD121373,PD-121373 | |
PD 121373 is a Benzothiopyrano-indazole cpd. The benzothiopyranoindazoles are potent inhibitors of nucleic acid synthesis, reducing both DNA and RNA synthesis to the same extent at similar concentrations. | |||
T28310 | PD 114595 | PD-114595,PD114595 | |
PD 114595 is a Benzothiopyrano-indazole cpd. PD 114595 belongs to a class of DNA complexers, PD 114595 has curative properties against murine solid tumor models. | |||
T80114 | FA-Ala-Arg | Endogenous Metabolite | |
FA-Ala-Arg is a dipeptide featuring a furylacryloyl group that degrades to yield arginine. It augments nitric oxide (NO) synthesis in MCF-7 cells through a mechanism in which cell-surface Carboxypeptidase-D (CPD) elevate... |
Cat No. | Product Name | Synonyms | Targets |
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TN3909 | Ebracteolata cpd B | Others | |
Ebracteolata cpd B is a natural product for research related to life sciences. The catalog number is TN3909 and the CAS number is 83459-37-4. | |||
T20200 | Citrulline malate | L-Citrulline DL-malate,Stimol | |
Citrulline malate is a cpd of anti-fatigue. |
Cat No. | Product Name | Species | Expression System |
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TMPH-01042 | Carboxypeptidase D Protein, Human, Recombinant (His & Myc) | Human | Baculovirus Insect Cells |
Carboxypeptidase D Protein, Human, Recombinant (His & Myc) is expressed in Baculovirus insect cells with N-10xHis and C-Myc tag. The predicted molecular weight is 12.3 kDa and the accession number is O75976. | |||
TMPH-01043 | Carboxypeptidase D Protein, Human, Recombinant (hFc & Myc) | Human | HEK293 Cells |
Carboxypeptidase D Protein, Human, Recombinant (hFc & Myc) is expressed in HEK293 mammalian cells with C-hFC-Myc tag. The predicted molecular weight is 37.3 kDa and the accession number is O75976. |