Cat. No. | Product name | CAS No. |
DC20407 |
HMPC
HMPC is a novel bacteriostatic agent that shows bacteriostatic activity against S. aureus (MIC=4 μg/ml) and rescues Caenorhabditis elegans from S. aureus infection. |
128202-97-1 |
DC22107 |
HMS-101
HMS-101 (HMS101) is a potent, selective mutant IDH1 inhibitor, the IC50 is significantly lower in mouse bone marrow cells transduced with IDH1mut compared with IDH1wt (1 uM vs 12 uM, respectively). |
1070690-06-0 |
DC9415 |
Hoechst 33342 (trihydrochloride)
Hoechst 33342 3Hcl(HOE 33342 3Hcl) is an AT-specific DNA minor groove ligand used fluorochrome for visualizing cellular DNA. |
875756-97-1 |
DC9418 |
Hoechst 33258 analog
Hoechst stains are part of a family of blue fluorescent dyes used to stain DNA. |
258843-62-8 |
DC22129 |
HOIPIN-1(JTP-0819958;HOIP inhibitor-1)
Featured
HOIPIN-1 (JTP-0819958, HOIP inhibitor-1) is a chemical inhibitor of linear ubiquitin chain assembly complex (LUBAC, IC50=2.8 uM), specifically generates Met1-linked linear ubiquitin chains through the ubiquitin ligase activity in HOIP, and activates the N |
|
DC22108 |
HOIPIN-8
HOIPIN-8 (HOIP inhibitor-8) is a potent chemical inhibitor of linear ubiquitin chain assembly complex (LUBAC, IC50=11 nM), specifically generates Met1-linked linear ubiquitin chains through the ubiquitin ligase activity in HOIP, and activates the NF-kB pa |
|
DC10177 |
Homoplantaginin
Homoplantaginin is a flavonoid from a traditional Chinese medicine Salvia plebeia with antiinfammatory and antioxidant properties. |
17680-84-1 |
DC12154 |
Hosenkoside A
Hosenkoside A is a baccharane glycoside isolated from the seeds of impatiens balsamina. |
156791-82-1 |
DC12148 |
Hosenkoside B
Hosenkoside B is a baccharane glycoside isolated from the seeds of impatiens balsamina. |
156764-82-8 |
DC12152 |
Hosenkoside F ((+)-Hosenkoside F)
Hosenkoside F is a baccharane glycoside isolated from the seeds of impatiens balsamina. |
160896-45-7 |
DC12153 |
Hosenkoside K
Hosenkoside K is a baccharane glycoside isolated from the seeds of impatiens balsamina. |
160896-49-1 |
DC12149 |
Hosenkoside M ((+)-Hosenkoside M)
Hosenkoside M is a baccharane glycoside isolated from the seeds of impatiens balsamina. |
161016-51-9 |
DC23978 |
hPGDS-IN-1
Featured
hPGDS-IN-1 is a potent, selective hPGDS inhibitor with IC50 of 12 nM in FP or EIA assays.. |
1234708-04-3 |
DC23894 |
HPI-1
Featured
HPI-1 is a Hedgehog (Hh) pathway inhibitor that suppresses signaling through Shh (IC50=1.5 uM) without significantly affecting Wnt signaling (IC50>30 uM). |
599150-20-6 |
DC12259 |
HS-10296 hydrochloride
HS-10296 hydrochloride is an orally available and third-Generation inhibitor of epidermal growth factor receptor (EGFR)-activating mutations and T790M-resistant mutation with limited activity against wild-type EGFR. |
2134096-03-8 |
DC11128 |
HS148
Featured
HS148 (DAPK3 inhibitor HS148) is a selective DAPK3 inhibitor with Ki of 119 nM, >10-fold selectivity over Pim kinases.. |
1892595-16-2 |
DC12616 |
HS-152
HS-152 (HS152) is a specific small-molecule inhibitor of SMAD ubiquitin regulatory factor 1 (SMURF1), not only potently inhibits SMURF1-mediated RHOB degradation with IC50 of 3.2 uM, but also strongly blocks SMURF1-mediated RHOA and SMAD1 degradation (IC5 |
|
DC7426 |
HS-173
Featured
HS-173 is a potent PI3Kα inhibitor with IC50 of 0.8 nM. |
1276110-06-5 |
DC12632 |
HS220
Featured
HS220 (HS-220) is a Plasmodium-selective takinib analog that targets atypical P. falciparum protein kinase 9 (PfPK9, Kd=4.1 uM) but does not inhibit HsTAK1, decreases K63-linked ubiquitination in P. falciparum; inhibits P. berghei parasite load in HuH7 ce |
1570374-32-1 |
DC11126 |
HS56
HS56 (Pim-DAPK3 inhibitor HS56) is a potent, dual Pim/DAPK3 inhibitor with Ki of 72 nM (Pim-3) and 315 nM (DAPK3), shows micromolar potency toward Pim-1 and Pim-2 (Ki=1.5 and 17 uM). |
922050-57-5 |
DC23784 |
HS-72
HS-72 is an allosteric, selective, cell-permeable inhibitor of inducible Hsp70 (Hsp70i or Hsp72), shows selectivity for Hsp70i over the closely related Hsc70 as well as the broader purinome. |
1800285-51-1 |
DC21126 |
HSD 1169
HSD1169 is a potent, dual FLT3/TOPK inhibitor with activity against FLT3-ITD secondary mutations (D835 or F691, Kd=1-5 nM), potently inhibits acute myeloid leukemia cell lines (IC50=5 nM). |