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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| 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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