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Other Targets

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Cat. No. Product Name Field of Application Chemical Structure
DC23116 (S)-GNE-140
The less active enantiomer of GNE-140, inhibits LDHA activity (18-fold less potent that (R)-GNE-140).
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DC10411 TB500-2
TB500-2 is one of the TB500 metabolites. TB500 is a synthetic version of an active region of thymosin β4. TB500 is claimed to promote endothelial cell differentiation, angiogenesis in dermal tissues, keratinocyte migration, collagen deposition and decreas
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DC20095 Target Protein-binding moiety 6 hydrochloride
Target Protein-binding moiety 6 hydrochloride is a compound that binds to BRD9, and used for inhibiting BRD9 activity, based on PROTAC.
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DC20048 TAK-828F
TAK-828F is a potent, selective, and orally available retinoic acid receptor-related orphan receptor γt (RORγt) inverse agonist (binding IC50=1.9 nM, reporter gene IC50=6.1 nM). TAK-828F shows excellent ROR isoforms selectivity (>5000-fold selectivity aga
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DC8880 Orteronel (TAK-700)
TAK-700 shows potent inhibitory activity against rat, monkey, and human steroid 17,20-lyase inhibitor with IC50 of 54 nM, 27 nM, and 38 nM, respectively.
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DC20117 SW-163D-AcLysValCit-PABC-DMAE
SW-163D-AcLysValCit-PABC-DMAE is a Drug-Linker Conjugates for ADC which consists of a natural bis-intercalator, SW-163D, conjugated via an AcLysValCitPABC-DMAE linker.
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DC20098 SRPKIN-1
SRPKIN-1 is a covalent and irreversible SRPK1/2 inhibitor with IC50s of 35.6 and 98 nM, respectively. Anti-angiogenesis effect.
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DC9767 SHR-1977 Featured
SHR-1977 is a novel ROMK/hERG inhibitor, (ROMK IC50 = 44 nM, hERG IC50 = >100,000 nM)
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DC20051 Sauristolactam (Saurolactam)
Sauristolactam, a natural aristolactam isolated from aerial portions of Saururus chinensis, has significant neuroprotective activity against glutamate-induced toxicity in primary cultured rat cortical cells. Sauristolactam also inhibits the receptor activ
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DC12391 BL-AD008 Featured
BL-AD008 (BL-AD 008) is a novel small molecule, dual-target activator targeting AMPK/ZIPK; demonstrates remarkable anti-proliferative activities toward cervical cancer cells and could induce apoptosis by death-receptor and mitochondrial pathways; also sho
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DC26066 BAY 61-3606 hydrochloride Featured
BAY 61-3606 is a potent, ATP-competitive, reversible, and highly selective inhibitor of Syk tyrosine kinase with Ki of 7.5 nM, displays no inhibitory effect against Btk, Fyn, Itk, Lyn, and Src.
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DC23086 Vandetanib hydrochloride
A potent and selective VEGFR2 (KDR) inhibitor with IC50 of 40 nM.
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DCZ-153 paclitaxtide
>98%,Standard References
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DCZ-129 Panax notoginsenosides
>98%,Standard References
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DCY-142 Ginkgolic acids
>98%,Standard References
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DCY-113 Acevaltratum
>98%,Standard References
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DCJ-050 3’-methoxy-5’-hydroxyisoflavone-7-O-β-D-glucoside
>98%,Standard References
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DCY-141 Yejunualactone
>98%,Standard References
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DCF-009 beta-rosasterol
>98%,Standard References
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DCY-129 Acetytastragaloside
>98%,Standard References
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DCS-112 Ochnaflavone7-O-β-D-gluco-pyranoside
>98%,Standard References
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DCS-097 1,3,5,8-Tetrahydroxylxanthone
>98%,Standard References
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DCY-175 Icarisid II
>98%,Standard References
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DCG-023 Epimeredinoside A
>98%,Standard References
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DCJ-068 Sanguinarine citrate
>98%,Standard References
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DCJ-060 3’-Methoxy apiin;Chrysoeiol-7-(2-O-apiosylglucoside)
>98%,Standard References
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DCJ-047 25-OCH3-Protopanaxtiol
>98%,Standard References
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DCY-090 beta-boswellic acid,3-acetyl,11-keto
>98%,Standard References
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DCY-089 alpha-boswellic acid,3-acetyl
>98%,Standard References
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DCS-085 R-Notoginsenoside R2
>98%,Standard References
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