Cat. No. | Product name | CAS No. |
DC73958 |
CU-76
CU-76 (cGAS inhibitor CU-76) is a small-molecule human cGAS (hcGAS) inhibitor with IC50 of 0.24 uM. |
2400954-58-5 |
DC73959 |
CW3388
CW3388 (CW-3388, CW3388) is a potent, cell-active Δ8,7-sterol isomerase (EBP) inhibitor, shows near-maximal effects on oligodendrocyte formation at 110 nM. |
414881-01-9 |
DC73960 |
CW4142
CW4142 (CW 4142) is a small molecule SC4MOL inhibitor that enhances oligodendrocyte formation. |
150199-99-8 |
DC73961 |
CW5107
CW5107 (CW 5107) is a small molecule HSD17B7 inhibitor that enhances oligodendrocyte formation. |
|
DC73962 |
Cytochalasin B
Cytochalasin B is a cell-permeable mycotoxin that inhibits network formation by actin filaments, inhibits cell movement and induces nuclear extrusion. |
14930-96-2 |
DC73963 |
DB2313
Featured
DB2313 is a small-molecule transcription factor PU.1 inhibitor abrogating DNA binding by PU.1 with Kd of 29 nM. |
2170606-74-1 |
DC73964 |
DC-SX029
DC-SX029 is a new small-molecule sorting nexin 10 (SNX10) inhibitor (KD=0.935 uM), blocks the SNX10-PIKfyve interaction, decreases TBK1/c-Rel signaling activation. |
300713-88-6 |
DC73965 |
DDIT
DDIT is a potent, non-toxic inhibitor of hyaluronan synthesis via targeting hyaluronan synthase (HAS), significantly suppresses the aggressiveness of triple-negative breast cancer cells grown in tissue culture. |
869355-30-6 |
DC73966 |
DDX3X helicase 64
DDX3X helicase 64 is a potent, selective inhibitor of DDX3X helicase activity with IC50 of 0.14 μM, shows promising anti-HCV activity, with an EC50 of 0.2 μM and cytotoxicity of 86 μM. |
|
DC73967 |
DDX3X helicase 79
DDX3X helicase 79 is a potent, selective inhibitor of DDX3X helicase activity with IC50 of 5 nM, shows antiviral activity against DENV-2 and WNV with EC50 of 1.6 and 2.3 uM, respectively. |
2414591-16-3 |
DC73968 |
DDX3X helicase 86
DDX3X helicase 87 is a potent, selective and aller inhibitor of DDX3X helicase activity with IC50 of 7 nM, shows antiviral activity against DENV-2 and WNV with EC50 of 6.3 and 0.88 uM, respectively. |
2571070-57-8 |
DC73969 |
DFO-5
DFO-5 (Oseltamivir Epoxy Impurity) is an oseltamivir impurity. |
204254-96-6 |
DC73970 |
DFTD
DFTD is a time-dependent, reversible and covalent inhibitor of eukaryotic elongation factor 2 kinase (eEF-2K) targeting of Cys-146, DFTD binds to the ATP binding site of eEF-2K. |
208254-22-2 |
DC73971 |
DHAB
DHAB is a potent, specific small molecule inhibitor of kidney ADPR-cyclase with IC50 of 2.5 nM, does not inhibit CD38, spleen, heart or brain ADPR-cyclase activity in vitro. |
51437-66-2 |
DC73972 |
DHC-156
DHC-156 is a covalent small molecule inhibitor of oncogenic transcription factor brachyury, selectively binds to brachyury, DHC-156 is potent brachyury downmodulator with DC50 of 4.1 uM. |
|
DC73973 |
Dibutepinephrine
Dibutepinephrine is a sympathomimetic compound. |
2735735-23-4 |
DC73974 |
Dichloroallyl lawsone
Dichloroallyl lawsone (Dichlorolapachol, DCL, NSC-126771) is a synthetic analogue of the antimalarial lapachol, inhibits mitochondrial dihydroorotate dehydrogenase (DHODH) with antineoplastic activity. |
36417-16-0 |
DC73975 |
Dihydrorhodamine 123
Dihydrorhodamine 123 (DHR 123) is a cell-permeable fluorogenic probe that is useful for the detection of reactive oxygen species (ROS) such as peroxide and peroxynitrite.. |
109244-58-8 |
DC73976 |
DiI
Dil (DiIC18(3)) is a fluorescent neuronal tracer that labels cell bodies, axons, dendrites, and dendritic spines. |
|
DC73977 |
DKC1125
DKC1125 is a small molecule KSRP-binding compound that specifically inhibits the oncogenic KITENIN complex, suppresses distant metastasis of colorectal cancer (CRC). |
|
DC73978 |
DS07551382
DS07551382 (DS 07551382) is potent, selective and orally active PTDSS1 (phosphatidylserine synthetase 1), suppresses phosphatidylserine (PS) production activity of PTDSS1 (IC50=100 nM) in cell-free assays, but not that of PTDSS2. |
2488609-68-1 |
DC73979 |
DS21150768
DS21150768 is a potent selective and orally active hematopoietic progenitor kinase 1 (HPK1) inhibitor with IC50 of 3.27 nM in cell-free HPK1 assays, binds to HPK1 with an affinity constant (KD) of 6.08 nM. |