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Search Results for " cpd "

Targets

37

Compounds

2

Natural Products

2

Recombinant Proteins

Cat No. Product Name Synonyms Targets
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...

Compounds

PDL-1 cpd 10
T9359
Synonym:
Target: PD-1/PD-L1
cpd.5 of 2234271-86-2
T9794
Synonym:
Target:
3,5-Diiodothyropropionic acid
T13492
Synonym: C082182,Ditpa cpd
Target: Thyroid hormone receptor(THR)
PTACH
T3199
Synonym: NCH-51,Cpd 51
Target: HIV Protease, HDAC
Cpd.4
T9547
Synonym:
Target: Others
Cpd.7 of 1326852-06-5
T9559
Synonym:
Target:
Cpd.5 of 1207358-59-5
T12123L
Synonym:
Target:
CPD2028
T8754
Synonym:
Target: Others
CPD-1224
T75140
Synonym:
Target:
CU-CPD107
T35349
Synonym: CU-CPD107
Target: TLR
MF 13
T33372
Synonym: MF13Cpd,MF13 Cpd,MF-13,MF13,MF13-Cpd
Target:
CPD3615-A5
T22298
Synonym:
Target: Others
Glutathione amide
T31949
Synonym: GASH cpd,L-gamma-Glutamyl-L-cysteinylglycinamide
Target:
(Rac)-X77
T8688
Synonym: CPD77,MUN91789
Target: SARS-CoV
AHR-activator-1023
T23686
Synonym: Branching Morphogenesis Modulator 1023,Cpd 1023,Compound 1023,BMM 1023
Target:
C188
T26936
Synonym: Cpd188,STAT3-IN-C188,Cpd-188,C 188,C-188
Target:
CPD7
T68310
Synonym:
Target:
CPD26
T69252
Synonym:
Target:
FPFS-1169 HCl
T31864
Synonym: R-(-)-BPAP,FPFS 1169,FPFS-1169 hydrochloride,BPAP-cpd,R-FPFS-1169,FPFS1169
Target:
ACT-281959
T71363
Synonym:
Target:
5-hydroxy Isatin
T71987
Synonym:
Target:
IQDMA
T69292
Synonym:
Target:
(E)-1,7,7-trimethyl-3-((3-(trifluoromethyl)phenyl)imino)bicyclo【2.2.1】heptan-2-one
T9539
Synonym:
Target:
CPDA
T10877
Synonym:
Target: Phosphatase
CPDS
T9807
Synonym:
Target: Others
trans-ACPD
T3484
Synonym: Trans-(±)-ACP,1-amino-1,3-dicarboxycyclopentane,(±)-trans-ACPD
Target: GluR
(1S,3R)-ACPD
T22488
Synonym:
Target: Others
NPEC-caged-(1S,3R)-ACPD
T23080
Synonym:
Target: Others
CPD7 HCl
T71989
Synonym:
Target:
CLK1/2-IN-3
T23897
Synonym: CLK1/2 inhibitor 3,CLK1/2-inhibitor-3,CLK1/2 IN 3,CLK1/2IN3
Target: CDK
BRD-6929
T10603
Synonym:
Target: HIV Protease, HDAC
Kenazepine
T32376
Synonym:
Target:
Sanazole
T34508
Synonym: AK2123,AK-2123,AK 2123
Target:
AGLME
T25007
Synonym: N-alpha-Acetylglycyllysyl methyl ester
Target:
PD 121373
T28320
Synonym: PD121373,PD-121373
Target:
PD 114595
T28310
Synonym: PD-114595,PD114595
Target:
FA-Ala-Arg
T80114
Synonym:
Target: Endogenous Metabolite
Cat No. Product Name Synonyms Targets
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.

Recombinant Proteins

Cat No. Product Name Species Expression System
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.
TargetMol