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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T4681 | T863 | DGAT-3,DGAT-1 inhibitor | Acyltransferase , Transferase |
T-863(DGAT-1 inhibitor) is an orally active, selective and potent DGAT1 (Acyl-CoA:diacylglycerol acyltransferase 1) inhibitor that interacts with the acyl-CoA binding site of DGAT1, and inhibits triacylglycerol synthesis... | |||
T7785 | T-1105 | Influenza Virus | |
T-1105 is a broad-spectrum antiviral inhibitor. | |||
T17846 | DOTA-(t-butyl)3-PEG5-azide | Others | |
DOTA-(t-butyl)3-PEG5-azide is a polyethylene glycol (PEG) derived linker designed specifically for the synthesis of proteolysis targeting chimeras (PROTACs)[1]. | |||
T6833 | Favipiravir | T-705,6-Fluoro-3-oxo-3,4-dihydropyrazine-2-carboxamide | Others , SARS-CoV , Influenza Virus , DNA/RNA Synthesis |
Favipiravir (T-705) (T-705), an effective and selective RNA-dependent RNA polymerase inhibitor, are applied to treat influenza virus infections. | |||
T24131 | HDAC3-IN-T247 | HDAC3 inhibitor T247,HDAC3 inhibitor-T247,HDAC3 IN T247,T247 | Histone Demethylase , Antiviral |
HDAC3-IN-T247 (HDAC3 inhibitor T247) is a selective and potent histone deacetylase 3 (HDAC3) inhibitor with anticancer and antiviral activities.HDAC3-IN-T247 induces NF-κB acetylation in human colon cancer HCT116 cells i... | |||
T13998 | 1-(t-Boc-Aminooxy)-3-aminooxy-propane | Others | |
1-(t-Boc-Aminooxy)-3-aminooxy-propane is an alkyl/ether-based PROTAC linker utilized in the synthesis of PROTACs[1]. | |||
T7578 | REVERSE T3 | 3,3',5'-triiodo-L-thyronine | Thyroid hormone receptor(THR) |
Reverse T3 (3,3',5'-triiodo-L-thyronine) inhibits the increase of sodium current generated by other thyroid hormone analogs in neonatal rat myocytes. | |||
T18656 | S-acetyl-PEG2-Boc | Tert-Butyl 3-[2-(2-Acetylsulfanylethoxy)Ethoxy]Propanoate,S-Acetyl-PEG2-T-Butyl Ester | Others , PROTAC Linker |
S-acetyl-PEG2-Boc (S-Acetyl-PEG2-T-Butyl Ester) is a PEG-based PROTAC linker. S-acetyl-PEG2-Boc can be used in the synthesis of PROTACs. | |||
T8656 | CAY10404 | 3-(4-METHYLSULPHONYLPHENYL)-4-PHENYL-5-T | Apoptosis , Akt , COX |
CAY10404 (3-(4-METHYLSULPHONYLPHENYL)-4-PHENYL-5-T) is a potent and highly selective inhibitor of COX-2 and COX-1. It is also a potent inhibitor of PKB/Akt and MAPK signalling pathways and induces apoptosis in NSC-LC cel... | |||
T1814 | ICILIN | AG-3-5 | TRP/TRPV Channel |
ICILIN (AG-3-5) is a synthetic TRPM8 ion channel super-agonist. | |||
T35719 | T2AA | T2AA,4-[4-[(2S)-2-amino-3-hydroxypropyl]-2,6-diiodophenoxy]phenol,ZINC95605533 | DNA/RNA Synthesis |
T2AA (4-[4-[(2S)-2-amino-3-hydroxypropyl]-2,6-diiodophenoxy]phenol) is an inhibitor of proliferating cell nuclear antigen (PCNA) with IC50 of 1 μM for PCNA/PIP-box peptide interaction. T2AA suppresses cancer cell growth ... | |||
T1653 | Liothyronine | Tresitope,O-(4-Hydroxy-3-iodophenyl)-3,5-diiodo-L-tyrosine,Triiodothyronine,L-3,3',5-Triiodothyronine,3,3',5-Triiodo-L-thyronine,Lyothyronine | Thyroid hormone receptor(THR) , Endogenous Metabolite |
Liothyronine (Tresitope) is an active form of thyroid hormone, binding to β1 thyroid hormone receptor (TRβ1), and activates its activity. | |||
TNU1269 | 3’-O-(t-Butyldiphenylsilyl)thymidine | ||
3'-O-(t-Butyldiphenylsilyl)thymidine is a Nucleoside Derivative - Protected nucleoside w/NH2/OH open. | |||
TNU0727 | 3’-O-t-Bulyldimethylsilyl thymidine | ||
Nucleosides - 2’-deoxynucleoside | |||
TNU0604 | 3’-O-t-Butyldimethylsilyl adenosine | ||
3'-O-t-Butyldimethylsilyl adenosine is a Nucleoside; Used for special nucleoside modification. | |||
T1669 | Liothyronine sodium | 3,3',5-Triiodo-L-thyronine sodium,Triostat,T3 Sodium salt,Sodium L-3,3',5-triiodothyronine,Cytomel | Thyroid hormone receptor(THR) |
Liothyronine Sodium is the sodium salt form of liothyronine, a synthetic form of the levorotatory isomer of the naturally occurring thyroid hormone triiodothyronine (T3). Liothyronine sodium (3,3',5-Triiodo-L-thyronine s... | |||
TNU0078 | N1-Methyl-N3-[(2S)-2-(t-butoxycarbonyl)amino-3-(t-butoxycarbonyl)] propylpseudouridine | ||
N1-Methyl-N3-[(2S)-2-(t-butoxycarbonyl)amino-3-(t-butoxycarbonyl)] propylpseudouridine is a Nucleoside Derivative - C-nucleoside; N-Alkylated nucleoside. | |||
T16969 | t-Boc-Aminooxy-PEG3-alcohol | Others | |
t-Boc-Aminooxy-PEG3-alcohol is a polyethylene glycol (PEG)-based linker compound commonly employed for the synthesis of proteolysis targeting chimeras (PROTACs)[1]. | |||
T24856 | t-Boc-aminooxy-PEG3-propargyl | ||
t-Boc-aminooxy-PEG3-propargyl is a crosslinker containing a propargyl group and a t-Boc-aminooxy group. PEG Linkers may be useful in the development of antibody-drug conjugates. | |||
TNU1137 | 3’-O-(t-Butyldimethylsilyl)-2’-deoxyadenosine | ||
3'-O-(t-Butyldimethylsilyl)-2'-deoxyadenosine is a Nucleoside Derivative - Protected nucleoside with NH2/OH group open. |