| DC8726 |
FLLL31
Featured
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FLLK31 is a potent and selective inhibitor of the STAT3 signaling pathway. |
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| DC7751 |
FLLL32
Featured
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FLLL32, a novel curcumin analogue, is a potent STAT3 inhibitor. |
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| DC8164 |
Gilteritinib(ASP2215)
Featured
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FLT3/AXL inhibitor |
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| DC8230 |
FLT3-IN-1(SKLB4771)
Featured
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FLT3-IN-1(SKLB4771) is a novel potent and selective Flt3 inhibitor with IC50 of 10 nM; against FLT3-ITD-expressing MV4-11 cells with IC50 of 6 nM. |
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| DC5889 |
Fludarabine
Featured
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Fludarabine (Synonyms: F-ara-A; NSC 118218) is a prodrug converted to free nucleoside 9-β-D-arabinosyl-2-fluoroadenine (F-ara-A). F-ara-A enters cells and accumulates as 5’-triphosphate. Interferes with DNA synthesis and repair. |
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| DC4190 |
Fludarabine phosphate
Featured
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Fludarabine Phosphate is an analogue of adenosine and deoxyadenosine, which is able to compete with dATP for incorporation into DNA and inhibit DNA synthesis. |
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| DC8337 |
Fluensulfone
Featured
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Fluensulfone is a new nematicide of the fluoroalkenyl thioether group that has significantly reduced environmental impact with low toxicity to non-target insects and mammals. |
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| DC11413 |
Flumatinib
Featured
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Flumatinib is a multi-kinase inhibitor with IC50 Values of 1.2 nM, 307.6 nM and 2662 nM for c-Abl, PDGFRβ and c-Kit respectively. |
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| DC8910 |
Flunarizine dihydrochloride
Featured
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Flunarizine is a selective calcium entry blocker. |
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| DC22475 |
FITC
Featured
|
Fluorescein isothiocyanate(FITC) is a derivative of fluorescein used in wide-ranging applications including flow cytometry. |
|
| DC10424 |
Fluorescein-5-maleimide
Featured
|
Fluorescein-5-maleimide is a fluorescent thiol-reactive dye used to conjugate fluorescein to proteins (excitation: 494 nm, emission: 519 nm). |
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| DC9669 |
Fluoroclebopride
Featured
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Fluoroclebopride is useful chemical for PET image study. |
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| DC9078 |
Fluoxetine Hydrochloride
Featured
|
Fluoxetine HCl is an antidepressant of the selective serotonin reuptake inhibitor (SSRI) class. |
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| DC9164 |
Flupenthixol dihydrochloride
Featured
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Flupenthixol dihydrochloride is a typical antipsychotic of the thioxanthene class that acts as an antagonist at dopamine D2 receptors (Ki = 0.38 nM) and an inverse agonist at serotonin 5-HT2A receptors (Ki = 7 nM).1 It has also been identified as an inhib |
|
| DC10158 |
Fluralaner
Featured
|
Fluralaner (INN) is a systemic insecticide and acaricide Fluralaner through potent blockage of GABA and L-glutamate gated chloride channels. |
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| DC12247 |
Fluspirilene (R 6218; Redeptin)
Featured
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Fluspirilene is a non-competitive antagonist of L-type calcium channels with an IC50 of 0.03 μM. Fluspirileneis a long-acting injectable depot antipsychotic drug used for schizophrenia. |
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| DC10020 |
Fluticasone furoate
Featured
|
Fluticasone furoate is a synthetic trifluorinated corticosteroid with potent anti-inflammatory activity. |
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| DC22228 |
Fluzoparib
Featured
|
Fluzoparib (SHR 3162) is a selective poly [ADP-ribose] polymerase 1 (PARP1) and poly [ADP-ribose] polymerase 2 inhibitor (PARP2), being developed by Jiangsu HengRui Medicine, for the treatment of cancer. PARP enzymes play a vital role in repair of DNA dam |
|
| DC10826 |
FM-381
Featured
|
FM-381 is a JAK3 specific reversible covalent inhibitor with IC50 of 127 pM for JAK3 and demonstrates 400-, 2,700- and 3,600-fold selectivity over JAK1, JAK2, and TYK2, respectively. |
|
| DC7937 |
LFM-A13
Featured
|
FM-A13 is a selective inhibitor of Bruton’s tyrosine kinase (BTK) – IC₅₀’s = 2.5 µM (recombinant BTK) and 17.2 µM (human BTK). |
|
| DC26027 |
FMF-04-159-2
Featured
|
FMF-04-159-2 is a covalent CDK14 inhibitor. FMF-04-159-2 inhibits CDK14 and CDK2 with IC50s of 39.6 nM and 256 nM in NanoBRET assay, respectively. |
|
| DC10194 |
FMK 9a
Featured
|
FMK 9a is an autophagin-1 inhibitor with IC50 values of 80 and 73 μM in FRET and LRA assay. |
|
| DC7696 |
FMK
Featured
|
Fmk is an irreversible ribosomal S6 kinase inhibitor 1/2 inhibitor. |
|
| DC8703 |
Fmoc-Val-Cit-PAB
Featured
|
Fmoc-Val-Cit-PAB is a linker for antibody-drug-conjugation (ADC). |
|
| DC8701 |
Fmoc-Val-Cit-PAB-PNP
Featured
|
Fmoc-Val-Cit-PAB-PNP is a peptide prodrug linker, is a linker for antibody-drug-conjugation (ADC). |
|
| DC21019 |
FOBISIN 101
Featured
|
FOBISIN 101 is a small molecule 14-3-3 protein-protein interaction inhibitor with IC50 of 9.3 and 16.4 uM for the binding of 14-3-3ζ or 14-3-3γ to PRAS40, respectively. |
|
| DC4207 |
Fondaparinux sodium
Featured
|
Fondaparinux sodium is a synthetic and specific inhibitor of activated Factor X (Xa). |
|
| DCAPI1249 |
Acesulfame Potassium
Featured
|
Acesulfame potassium is an artificial sweetener. Acesulfame potassium (long-term) affects cognitive functions, potentially via altering neuro-metabolic functions in mice. |
|
| DC8285 |
Acotiamide HCl
Featured
|
Acotiamide monohydrochloride trihydrate is an orally active and first-in-class gastroprokinetic agent for the treatment of functional dyspepsia. Acotiamide monohydrochloride trihydrate enhances acetylcholine released by enteric neurons through muscarinic |
|
| DC7849 |
DTP3
Featured
|
For the detailed information of DTP3, the solubility of DTP3 in water, the solubility of DTP3 in DMSO, the solubility of DTP3 in PBS buffer, the animal experiment (test) of DTP3, the cell expriment (test) of DTP3, the in vivo, in vitro and clinical trial test of DTP3, the EC50, IC50,and affinity,of DTP3, Please contact DC Chemicals.. |
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