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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC42983 | Tormentic acid |
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| DC42982 | Pomolic acid |
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| DC42980 | Atroscine |
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| DC42977 | 6-O-Feruloylglucose |
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| DC42976 | Poricoic acid A(F) |
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| DC42974 | 6-O-Caffeoylarbutin |
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| DC42973 | Lobetyol |
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| DC42972 | trans-pDMA |
Effective constitutive androstane receptor (CAR) activator; Inhibitor of the gluconeogenic genes PEPCK and G6Pase through suppression of HNF4a and FOXO1 transcriptional activity
More description
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| DC42971 | ent-3-Oxokaurane-16,17-diol |
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| DC42970 | Cudraxanthone L |
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| DC42968 | ML138 |
Selective agonist of kappa opioid receptors (KOR)
More description
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| DC42967 | CEP-28122 Mesylate |
A highly potent, selective and orally active ALK inhibitor
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| DC42966 | 8-Prenyldaidzein |
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| DC42964 | CEP-33779 |
A highly selective, orally active inhibitor
More description
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| DC42963 | 5,7-Di-O-methylquercetin |
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| DC42962 | Discodermide |
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| DC42961 | Soyasaponin Ac |
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| DC42960 | Apigenin 4'-O-rhamnoside |
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| DC42959 | Heudelotinone |
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| DC42957 | UBP710 |
Selective modulator of NMDA receptors, potentiates responses at GluN1/GluN2A and GluN1/GluN2B
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| DC42956 | S4 |
A potent and selective inhibitor against sulfamate carbonic anhydrase (CA) subtypes CAIX & CAXII (Ki = 2, 7, 546, 5600 nM against human CA XII, IX, II, and I, respectively). S4 selectively inhibits migration upon anoxia/hypoxia-induced CAIX expression in
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| DC42955 | N-Allylnormetazocine hydrochloride |
Selective σ1 receptor agonist.
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| DC42954 | Macrocarpal A |
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| DC42953 | 9-Hydroxy-13E-labden-15-oic acid |
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| DC42952 | Terchebulin |
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| DC42951 | L-687414 |
Selective, low intrinsic activity, partial agonist at the glycine site of the N-methyl-D-aspartate (NMDA) receptor
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| DC42950 | IMZ-SnBu3 |
A presursor of Iodine-123 labeled Iomazenil as a SPECT imaging agent
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| DC42949 | 15-Demethylplumieride |
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| DC42948 | 4-Epialyxialactone |
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| DC42947 | Dihydrocucurbitacin B |
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