About 8 results found for searched term "DDa-1" (0.119 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M9862 | Desmopressin diacetate | Others |
| DDAVP; CAS# 16679-58-6 | ||
| Desmopressin diacetate is a selective and potent vasopressor agent that stabilizes the cardiocirculatory function in normal human as well as in patients suffering from catecholamine-resistant vasodilatory shock. | ||
| M43176 | DDa-1 | Others |
| DDa-1 is a potent kinase degrader. | ||
| M14480 | Toddalolactone | PAI-1 |
| Toddalolactone, a main component of Toddalia asiatica, inhibits the activity of recombinant human plasminogen activator inhibitor-1 (PAI-1), with an IC50 value of 37.31 μM. | ||
| M27736 | Lometrexol | Antifolate |
| DDATHF | ||
| Lometrexol (DDATHF), an antipurine antifolate, can inhibit the activity of glycinamide ribonucleotide formyltransferase (GARFT) but do not induce detectable levels of DNA strand breaks. Lometrexol can further inhibit de novo purine synthesis, causing abnormal cell proliferation and apoptosis, even cell cycle arrest. Lometrexol has anticancer activity. Lometrexol also is a potent human Serine hydroxymethyltransferase1/2 (hSHMT1/2) inhibitor. | ||
| M27935 | Lometrexol disodium | Antifolate |
| DDATHF disodium | ||
| Lometrexol (DDATHF) disodium, an antipurine antifolate, can inhibit the activity of glycinamide ribonucleotide formyltransferase (GARFT) but do not induce detectable levels of DNA strand breaks. Lometrexol disodium can further inhibit de novo purine synthesis, causing abnormal cell proliferation and apoptosis, even cell cycle arrest. Lometrexol disodium has anticancer activity. Lometrexol disodium also is a potent human Serine hydroxymethyltransferase1/2 (hSHMT1/2) inhibitor. | ||
| M28430 | Lometrexol hydrate | Antifolate |
| DDATHF hydrate | ||
| Lometrexol (DDATHF) hydrate, an antipurine antifolate, can inhibit the activity of glycinamide ribonucleotide formyltransferase (GARFT) but do not induce detectable levels of DNA strand breaks. Lometrexol hydrate can further inhibit de novo purine synthesis, causing abnormal cell proliferation and apoptosis, even cell cycle arrest. Lometrexol hydrate has anticancer activity. Lometrexol hydrate also is a potent human Serine hydroxymethyltransferase1/2 (hSHMT1/2) inhibitor. | ||
| M55786 | ML328 | Antibiotic |
| ML328 is a selective inhibitor of bacterial AddAB and RecBCD helicase-nucleases with IC50 values of 26 and 5.1 μM, respectively. | ||
| M55775 | CID 697851 | Antibiotic |
| CID 697851 is an AddAB and RecBCD inhibitor, with IC50s of 13 and 33 nM. | ||
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