| DC9651 |
Ingenol 3-angelate
Featured
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Ingenol 3-Angelate is a PKC(protein kinase C)activator; anti-cancer drug and an active ingredient in Euphorbia peplus. |
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| DC9653 |
Ingenol 5,20-Acetonide |
Ingenol 5,20-Acetonide (CAS 77573-43-4) |
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| DC9654 |
Ingenol 5,20-Acetonide-3-O-angelate |
Ingenol 5,20-Acetonide-3-O-angelate (CAS 87980-68-5) |
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| DC9646 |
Ingenol
Featured
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Ingenol is an extremely weak protein kinase C (PKC) activator. |
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| DC9652 |
Ingenol-3,4:5,20-diacetonide |
Ingenol-3,4:5,20-diacetonide (CAS 77573-44-5) |
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| DC22212 |
RNF5 INHIBITOR INH-02
Featured
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inh-02 (RNF5 inhibitor inh-02) is a novel small molecule inhibitor of E3 ubiquitin ligase RNF5/RMA1. |
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| DC7640 |
INH1 |
INH1 is a cell-permeable Hec1 inhibitor, which specifically disrupts the Hec1/Nek2 interaction. |
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| DC21704 |
Inh2-B1 |
Inh2-B1 (STK1 inhibitor B1) is a novel specific S aureus Ser/Thr protein kinase (STK1) inhibitor with IC50 of 49 uM, directly binds to ATP-binding catalytic domain. |
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| DC7479 |
Tiplaxtinin(PAI-039)
Featured
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Inhibitor of plasminogen activator inhibitor-1 (PAI-1) |
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| DCAPI1453 |
IBANDRONATE SODIUM |
Inhibits bone resorption as a sodium salt and complexed with technetium Tc 99m for bone imaging. The monophosphonates are not active and the biphosphonates are used in disorders affecting the skeleton such as metastatic disease, asteoporosis and Paget's. |
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| DC8132 |
TAPI-0 (TNF-α processing inhibitor-0) |
Inhibits TNF-α processing. Also a general matrix metalloprotease and TACE inhibitor. |
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| DC23238 |
INO-1001 |
INO-1001 is a potent, selective poly(ADP-ribose) polymerase (PARP) with IC50 of <50 nM in CHO cells. |
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| DC20417 |
iNOS inhibitor 12 |
iNOS inhibitor 12 is a potent, highly selective iNOS inhibitor with IC50 of 79 nM, dispalys almost 100-fold selectivity over eNOS and nNOS.. |
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| DC12101 |
Insulin levels modulator |
Insulin levels modulator could be used to treat diabetes. |
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| DC22513 |
INT-767 |
INT-767 is a potent, selective, dual farnesoid X receptor (FXR) and TGR5 agonist with EC50 of 30 and 630 nM, respectively. |
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| DC12106 |
Interferon receptor agonist |
Interferon receptor agonist is an interferonm (IFN) receptor agonist. |
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| DCAPI1381 |
Inulin |
Inulin |
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| DC12160 |
Iodipamide (Adipiodone) |
Iodipamide is a tri-iodinated benzoate derivative and ionic dimeric contrast agent used in diagnostic imaging. |
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| DC20420 |
Ionomycin calcium salt |
Ionomycin is an ionophore produced by the bacterium Streptomyces conglobatus, used in research to raise the intracellular level of calcium (Ca2+) and as a research tool to understand Ca2+ transport across biological membranes. |
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| DC20419 |
Ionomycin |
Ionomycin is an ionophore produced by the bacterium Streptomyces conglobatus. |
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| DC9564 |
Iopamidol |
Iopamidol is a nonionic, low-osmolar iodinated contrast agent.
|
|
| DC5070 |
IOX2
Featured
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IOX 2 is a potent inhibitor of HIF-1α prolyl hydroxylase-2 (PHD2) (IC50 = 21 nM). IOX 2 displays over 100-fold selectivity for PHD2 over factor inhibiting HIF-1 (FIH-1) and histone demethylases. |
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| DC21756 |
IP6K1 inhibitor TNP
Featured
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IP6K1 inhibitor TNP is a potent, selective inositol hexakisphosphate kinase IP6K with IC50 of 0.47 uM (IP6K1), does not inhibit either human or yeast Vip/PPIP5K. |
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| DC9575 |
IPA-3 |
IPA-3 is a selective non-ATP competitive PAK1 inhibitor with IC50 of 2.5 μM, no inhibition to group II PAKs (PAKs 4-6).
|
|
| DC12599 |
IPI-9119 |
IPI-9119 (IPI9119) is a potent, selective, and irreversible inhibitor of fatty acid synthase (FASN) with IC50 of 0.3 nM in biochemical assays. |
|
| DC20667 |
Ipidacrine hydrochloride hydrate |
Ipidacrine hydrochloride hydrate is a reversible acetylcholinesterase (AChE) inhibitor that directly stimulates impulse transmission in the central nervous system and neuromuscular synapses by blocking membrane potassium channels. |
|
| DC20666 |
Ipidacrine hydrochloride |
Ipidacrine hydrochloride is a reversible acetylcholinesterase (AChE) inhibitor that directly stimulates impulse transmission in the central nervous system and neuromuscular synapses by blocking membrane potassium channels. |
|
| DCAPI1117 |
Ipratropium bromide |
Ipratropium bromide |
|
| DC10295 |
IPSU
Featured
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IPSU is a selective, orally available and brain penetrant OX2R antagonist with a pKi of 7.85. |
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| DC23614 |
IQM-266(IQM 266;IQM266) |
IQM-266 (IQM266) is a DREAM (Downstream Regulatory Element Antagonist Modulator) ligand (Kd=4.63 uM), inhibits the KV4.3/DREAM current in a concentration-, voltage-, and time-dependent-manner. |
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