| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCS-091 | Cephalomannine | >98%,Standard References |
|
| DCC-002 | Vinblastine | >98%,Standard References |
|
| DCQ-004 | 4'-Demethylepipodophyllotoxin | >98%,Standard References |
|
| DCJ-030 | Galanthamine | >98%,Standard References |
|
| DCW-011 | Evocarpine | >98%,Standard References |
|
| DCL-027 | Lipoic acid Featured | Lipoic acid is a selective, small molecule large-conductance Ca(2+)-activated K(+) channel (BKCa, KCa1.1, MaxiK) positive modulator with EC50 of 11 uM. Lipoic acid shows a favorable selectivity profile on Nav, Cav, SK, and IK channels. Lipoic acid causes distinct activation from a concentration of 0.3 and 10 µM Lipoic acid left-shifted the voltage activation curve by 60 mV. Lipoic acid reduces spontaneous phasic contractions in guinea pig urinary bladder strips at 1 uM, while having only a modest effect on contractions evoked by electrical field stimulation (EFS) and no effect on high K+-induced contractions. |
|
| DC22287 | Atractylenolide I Featured | Atractylenolide I is a sesquiterpene derived from the rhizome of Atractylodes macrocephala, possesses diverse bioactivities, such as neuroprotective, anti-allergic, anti-inflammatory and anticancer properties. Atractylenolide I reduces protein levels of phosphorylated JAK2 and STAT3 in A375 cells, and acts as a TLR4-antagonizing agent. |
|
| DC23034 | Isochlorogenic acid C Featured | 4,5-Dicaffeoylquinic acid ( Isochlorogenic acid C) possesses potent hepatoprotective and anti-HBV effects.IC50 value:Target: Anti-hepatitis natural produce.In vitro: To study anti-hepatitis effect of isochlorogenic acid C, anti-apoptotic and anti-injury properties of test compound were evaluated. The results showed that test compound at concentrations of 10 to 100 μg/ml significantly reduced the caspase-3 and transformed growth factor β1 (TGFβ1) levels of the D-GalN-challenged hepatocytes. Also, test compound improved markedly cell viability of the D-GalN-injured hepatocytes and produced a maximum protection rate of 47.28% at a concentration of 100 μg/ml. Furthermore, test compound significantly inhibited productions of HBsAg and HBeAg. Its maximum inhibitory rates on the HBsAg and HBeAg expressions were 86.93 and 59.79%, respectively. In addition, test compound significantly induced the HO-1 expression of HepG2.2.15 cells [1]. In vivo: |
|
| DCF-029 | Columbamine | >98%,Standard References |
|
| DCG-045 | Nardosinone | >98%,Standard References |
|
| DCL-036 | Glucosamine sulfate | >98%,Standard References |
|
| DCZ-276 | 5-Hydroxy-1-tetralone | >98%,Standard References |
|
| DCZ-277 | Methyl 4-hydroxycinnamate | >98%,Standard References |
|
| DCZ-104 | 4-HYDROXY-3-METHOXYCINNAMALDEHYDE | >98%,Standard References |
|
| DCL-018 | 2-Methoxycinnamic acid | >98%,Standard References |
|
| DCY-044 | 3-Hydroxy-4-methoxycinnamic acid | >98%,Standard References |
|
| DCJ-059 | Inosine | >98%,Standard References |
|
| DCH-024 | cis-Anethol | >98%,Standard References |
|
| DCF-022 | 4-(4-Hydroxyphenyl)-2-butanone | >98%,Standard References |
|
| DCY-147 | Isoeugenol | >98%,Standard References |
|
| DCD-064 | Eugenol | >98%,Standard References |
|
| DCZ-272 | Isopropyl 4-Hydroxybenzoate | >98%,Standard References |
|
| DCN-003 | Propylparaben | >98%,Standard References |
|
| DCB-027 | Cantharidin | >98%,Standard References |
|
| DCX-067 | 2,4,5-Trimethoxybenzaldehyde | >98%,Standard References |
|
| DCS-021 | Gallic acid trimethyl ether | >98%,Standard References |
|
| DCM-019 | Propyl gallate | Propyl gallate is a common food antioxidant. Propyl gallate can inhibit the production of acrolein, glyoxal and methylglyoxal. |
|
| DCB-003 | 2-Hydroxyadenosine | >98%,Standard References |
|
| DCN-021 | Guanosine | >98%,Standard References |
|
| DCD-037 | 4-Isopropyltoluene | >98%,Standard References |
|
