Cat. No. | Product name | CAS No. |
DC9444 |
5-R-Rivaroxaban
5-R-Rivaroxaban is (R) enantiomer of Rivaroxaban. |
865479-71-6 |
DC20195 |
6-(Dimethylamino)purine;N,N-Dimethyladenine
6-Dimethylaminopurine is a serine threonine protein kinase inhibitor. It inhibits the germinal vesicle breakdown and the meiotic maturation of oocytes. |
938-55-6 |
DC23336 |
6-Ethylthioinosine
6-Ethylthioinosine (6-ETI. |
13286-04-9 |
DC20604 |
6-FABA
6-FABA (6-Fluoroanthranilic Acid) is a small-molecule inhibitor of MTB tryptophan synthesis that converts Mtb into a tryptophan auxotroph and restores the efficacy of a failed host defense. |
434-76-4 |
DC9376 |
6-FITC
6-Fluorescein isothiocyanate(6-FITC) is a derivative of fluorescein used in wide-ranging applications including flow cytometry. |
3326-31-6 |
DC12326 |
6-Hydroxybentazon (6-Hydroxybentazone)
6-Hydroxybentazon is a phase I metabolite of bentazone, and bentazone is a chemical for use in herbicides. |
60374-42-7 |
DC20297 |
6-Hydroxy-DL-DOPA
Featured
6-Hydroxy-DL-DOPA is a small-molecule that disrupts with RAD52 oligomerization, inhibits ssDNA binding by RAD52 with IC50 of 1.1 uM and by RAD52 (1 209) with IC50 of 1.6 uM. |
21373-30-8 |
DC8864 |
6-Mercaptopurine (6-MP) Monohydrate
6-Mercaptopurine Monohydrate is a widely used antileukemic agent and immunosuppressive drug that inhibits de novo purine synthesis through incorporation of thiopurine methyltransferase metabolites into DNA and RNA. |
6112-76-1 |
DC12540 |
6-MOMIPP
6-MOMIPP is a novel microtubule disruptor that targets the colchicine binding site on β-tubulin, induces mitotic arrest, caspase activation and loss of cell viability of U251 glioblastoma in vitro. |
1961272-45-6 |
DC10215 |
7,8-Dihydroxyflavone
7,8-Dihydroxyflavone acts as a potent and selective small-molecule agonist of the TrkB receptor (Kd ≈ 320 nM), the main signaling receptor of brain-derived neurotrophic factor (BDNF). |
38183-03-8 |
DC12463 |
7-BIA
7-BIA is a small molecule 7-butoxy illudalic acid analog that targets receptor-type protein tyrosine phosphatase D (PTPRD, IC50=1-3 uM) with some specificity. |
1313403-49-4 |
DC12215 |
7-Dehydrocholesterol
7-Dehydrocholesterol is biosynthetic precursor of cholesterol and vitamin D3. |
434-16-2 |
DC21513 |
7DG
7DG (7-Desacetoxy-6,7-dehydrogedunin) is a selective inhibitor of protein kinase R (PKR) that directly interact with the C-terminal of PKR. |
26927-01-5 |
DC26033 |
8-Hydroxy-efavirenz
Featured
8-Hydroxy-efavirenz is the primary metabolite of the antiretroviral drug Efavirenz, stimulates the glycolytic flux in cultured rat astrocytes. |
205754-33-2 |
DC10186 |
8-O-Acetyl shanzhiside methyl ester
8-O-Acetyl shanzhiside methyl ester (ND01) is an iridoid glucoside isolated from the leaves of Lamiophlomis rotata Kudo, a Chinese folk medicinal plant in Xi-zang. |
57420-46-9 |
DC11964 |
Lys01
A 10-fold more potent lysosomal autophagy inhibitor than hydroxychloroquine (HCQ).. |
391426-22-4 |
DC20669 |
Imexon
A 2-cyanoaziridine derivative with antitumor activity in some types of cancer, including pancreatic, lung, breast, prostate, melanoma, and multiple myeloma. |
59643-91-3 |
DC23303 |
A 385358
A 385358 is a potent, selective, cell-permeable Bcl-XL inhibitor with Ki of 0.8 nM, displays >80-fold selectivity over Bcl-2 (Ki=64 nM). |
406228-55-5 |
DC24006 |
Nucleoside-Analog-2
A 4′-azidocytidine analogue that shows anti-HCV activity.. |
876708-01-9 |
DC24009 |
Nucleoside-Analog-1
A 4′-azidocytidine analogue that shows anti-HCV activity.. |
876707-99-2 |
DC7038 |
A 922500
Featured
A 922500 is a potent, selective, and orally bioavailable DGAT-1 inhibitor with IC50 values of 7 nM and 24 nM for human and mouse DGAT-1 respectively. |
959122-11-3 |
DC22355 |
Lisinopril
A angiotensin-converting enzyme (ACE) inhibitor for treatment of hypertension, heart failure, and after heart attacks.. |
76547-98-3 |