13
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T60002 | DC-S239 | Histone Methyltransferase | |
DC-S239 (DC-S239) is a selective inhibitor of histone methyltransferase SETD7 (IC50 = 4.59 μM) with anticancer activity. | |||
T10972 | DC4 | Others | |
DC4 can be used to synthesize antibody-drug conjugate (ADC), which is an ADC cytotoxin. DC4 can be used for targeted therapy of tumors. | |||
T37147 | 5'-O-DMT-N4-Ac-dC | 5'-O-DMT-N4-Ac-dC | |
5'-O-DMT-N4-Ac-dC (N4-Acetyl-2'-deoxy-5'-O-DMT-cytidine, compound 7) is a deoxynucleoside utilized in the synthesis of dodecyl phosphoramidite. Dodecyl phosphoramidite serves as a crucial precursor for dod-DNA production... | |||
T37136 | 5'-O-DMT-N4-Ac-2'-F-dC | 5’-O-DMT-N4-Ac-2’-F-dC | |
5’-O-DMT-N4-Ac-2’-F-dC is a modified nucleoside and can be used to synthesize DNA or RNA. | |||
T37138 | 5'-O-DMT-N4-Bz-5-Me-dC | 5’-O-DMT-N4-Bz-5-Me-dC | |
5’-O-DMT-N4-Bz-5-Me-dC is a modified nucleoside. 5’-O-DMT-2’-O-TBDMS-rI can be used in the synthesis of deoxyribonucleic acid or nucleic acid. | |||
T37137 | 5'-O-DMT-N4-Bz-2'-F-dC | 5’-O-DMT-N4-Bz-2’-F-dC | |
5’-O-DMT-N4-Bz-2’-F-dC is a nucleoside with protective and modification effects. | |||
T40783 | N4-Benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-deoxycytidine | 5'-O-DMT-N4-Bz-dC | |
N4-Benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-deoxycytidine, also known as 5'-O-DMT-N4-Bz-dC, is a chemical compound utilized in the synthesis of oligodeoxynucleotides that incorporate a 3'-S-phosphorothiolate (3'-PS) linkag... | |||
TN3801 | Methoxyphenoxy]oxane-3,4,5-triol | Dehydrodiconiferyl alcohol 4-O-beta-D-glucopyranoside | Others |
Dehydrodiconiferyl alcohol 4-O-beta-D-glucopyranoside is a natural product from Ligusticopsis wallichiana (DC) Pimenov & Kljuykov. | |||
T19773 | Diethyl bipy55'DC | ||
Diethyl bipy55'DC inhibits CP4H activity in cultured cells. The stability of collagen relies on post-translational modifications, the most prevalent being the hydroxylation of collagen strands by collagen prolyl 4-hydrox... | |||
T63315 | IRAK4-IN-19 | ||
IRAK4-IN-19 is a potent inhibitor of interleukin 1 receptor-associated kinase 4 (IRAK4) (IC50: 4.3 nM).IRAK4-IN-19 inhibits LPS-induced IL23 production in THP and DC cells and suppresses the development of arthritis in a... | |||
T39930 | MS98 | ||
MS98 is a highly effective and specific PROTAC AKT degrader compound that effectively targets and depletes total AKT (T-AKT) within cells, exhibiting a DC 50 value of 78 nM. This compound readily binds to AKT1, AKT2, and... | |||
T62950 | IRAK4-IN-18 | ||
IRAK4-IN-18 is a potent inhibitor of interleukin 1 receptor-associated kinase 4 (IRAK4) (IC50: 15 nM). IRAK4-IN-18 inhibits LPS-induced IL23 production in THP and DC cells and blocks the development of arthritis in rats,... | |||
T37880 | OPC-167832 | ||
OPC-167832 is a potent and orally active dprE1 Inhibitor with an IC50 of 0.258 μM. OPC-167832 has antituberculosis activity and can be used for the research of tuberculosis caused by Mycobacterium tuberculosis[1]. OPC-16... |