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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC47831 | Sanggenone H |
Sanggenone H is found in Morus alba L.
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| DC47825 | Oleoside 11-methyl ester |
Oleoside 11-methyl ester is a secoiridoid glucoside and possesses a strong cytotoxic activity against Hep-G2 cells.
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| DC47820 | Methyl p-hydroxyphenyllactate |
Methyl p-hydroxyphenyllactate (MeHPLA) is an important cell growth-regulating agent which binds to nuclear type II binding sites in normal and malignant cells.
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| DC47818 | Pinosylvin monomethyl ether |
Pinosylvin monomethyl ether has antibacterial effect and fungicidal activity.
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| DC47816 | Kulinone |
Kulinone has cytotoxic effects against A549, H460 and HGC27 with IC50 values of 6.2 ± 0.1, 7.8 ± 1.2, 5.6 ± 0.2 μg/ml。
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| DC47815 | Samwirin A |
Samwirin A is a promising radical scavenger in aqueous media at physiological pH.
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| DC47814 | Suomilide |
Suomilide inhibits human trypsin-2 and -3, with IC50 values of 4.7 and 11.5 nM, respectively, while trypsin-1 is inhibited with an IC50 of 104 nM.
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| DC47806 | Rhodiocyanoside A |
Rhodiocyanoside A is found to show antiallergic activity in a passive cutaneous anaphylaxis test in rat.
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| DC47804 | Rocaglaol |
Rocaglaol induces apoptosis and cell cycle arrest in LNCaP cells.
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| DC47802 | Rotundatin |
Rotundatin is useful in inhibition of the aggregation of platelets induced by arachidonic acid and collagen.
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| DC47800 | Monnieriside G |
Monnieriside G is found in Cnidium monnieri fruits.
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| DC47799 | Methylsyringin |
Methylsyringin exhibits anti-inflammatory activity in the LPS-stimulated RAW264.7 cells.
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| DC47798 | Rutaretin |
Rutaretin is found in Atalantia racemosa.
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| DC47795 | Quebecol |
Quebecol is a nutraceutical agent against periodontitis.
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| DC47793 | Peucedanocoumarin II |
Peucedanocoumarin II can induce rice resistance to blast disease.
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| DC47791 | OJV-VI |
OJV-VI is found in ophiopogonis.
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| DC47789 | Schisanwilsonin B |
Schisanwilsonin B is a lignan from the fruits of Schisandra wilsoniana.
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| DC47786 | Moscatin |
Moscatin inhibits AA-induced platelet aggregation in a concentration-dependent manner with IC50 values 37.2 μM .
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| DC47784 | Olivil monoacetate |
Olivil monoacetate is found in Gymnosporia varialilis Loes.
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| DC47783 | Mulberrofuran Q |
Mulberrofuran Q inhibits the formation of 12-hydroxy-5,8,10-heptadecatrienoic acid (HHT) and thromboxane B2 (cyclooxygenase products).
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| DC47533 | Nurr1 agonist 1 |
Nurr1 agonist 1 is an inverse agonist tool for the neuroprotective transcription factor Nurr1.
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| DC47532 | Oxythiamine diphosphate ammonium |
Oxythiamin diphosphate ammonium is a potent transketolase (TK) inhibitor.
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| DC47530 | SLK/STK10-IN-1 |
SLK/STK10-IN-1 is a potent and selective inhibitor of SLK and STK10 with nanomolar potency.
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| DC47529 | SPOP-IN-6b dihydrochloride |
SPOP-IN-6b dihydrochloride is a potent speckle-type POZ protein (SPOP) inhibitor with an IC50 of 3.58 μM.
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| DC47527 | Sinbaglustat |
Sinbaglustat (OGT2378) is a dual inhibitor of glucosylceramide synthase (GCS) and non-lysosomal glucosyl ceramidase (GBA2). Sinbaglustat is an orally available N-alkyl iminosugar that crosses the blood-brain barrier. Sinbaglustat can be used for the research of central neurodegenerative diseases associated with lysosomal dysfunctions.
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| DC47526 | R-(+)-Cotinine |
R-(+)-Cotinine ((+)-Cotinine), a Nicotine metabolite, lacks significant activity across a wide range of pharmacological targets. R-(+)-Cotinine can enhance the Ach-evoked current in human α7 nAChRs.
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| DC47520 | Peptide 78 |
Peptide 78, a chemotactic cytokine, a 78 amino acid protein member of the IL-8 or C-X-C chemokine supergene family. ENA-78 plays an important role in the elicitation of predominantly neutrophils (PMNs) into the joints of rheumatoid arthritis (RA).
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| DC47518 | TIM-3-IN-1 |
TIM-3-IN-1 represents useful tool to further study the biology of TIM-3 immune modulation in cancer.
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| DC47517 | PREP inhibitor-1 |
PREP inhibitor-1 is a highly potent prolyl oligopeptidase (PREP) inhibitor (IC50 < 1 nM).
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| DC47515 | MEIS-IN-3 |
MEIS-IN-3 is a potent myeloid ecotropic viral integration site (MEIS) inhibitor.
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