Natural Products
| Catalog No. | Information |
| CFN92906 | Neophellamuretin Neophellamuretin is a natural product from Akschindlium godefroyanum (Kuntze) H. Ohashi. |
| CFN92907 | Epimedonin B Epimedonin B is a natural product from Epimedium koreanum. |
| CFN92908 | (-)-Hydroxydihydrobovolide (-)-Hydroxydihydrobovolide is a natural product from Clausena emarginata Huang. |
| CFN92909 | Drynachromoside A Drynachromoside A exhibits the biochemical effects on the proliferation of MC3T3-E1 cells. |
| CFN92910 | Monnieriside A Monnieriside A is a natural product from Drynaria fortunei. |
| CFN92911 | Spiranthol A Reference standards. |
| CFN92912 | Licoricesaponin E2 Licoricesaponin E2 displayed the inhibition on the growth of cancer cells with IC50 at 18.3-41.6 umol/L, it could significantly increase the cytotoxic activity after hydrolysis. |
| CFN92913 | Uralsaponin D Uralsaponin D displayed the inhibition on the growth of cancer cells with IC50 at 18.3-41.6 μmol/L, it could significantly increase the cytotoxic activity after hydrolysis. |
| CFN92914 | 24-Hydroxy-licoricesaponin A3 Reference standards. |
| CFN92915 | Licoricesaponin G2 Licoricesaponin G2 has the anti-inflammatory effects as NF-κB inhibitors, it has anti-HIV activity via significantly interacted with R15K. |
| CFN92916 | Silybin B Silybin B and silybin A are potent inhibitors of both raloxifene 4'- and 6-glucuronidation in all enzyme systems; they show strong effects on cell growth inhibition and apoptosis induction in human chronic myeloid leukemia K562 cells. Silybin B exhibits 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activity. |
| CFN92917 | 8-O-Methylretusin-7-O-beta-D-glucopyranoside 8-O-Methylretusin-7-O-beta-D-glucopyranoside shows significant antimicrobial activity with a broad spectrum as well as antioxidant activity. |
| CFN92918 | Licopyranocoumarin Licopyranocoumarin could as a potent neuroprotective drug via markedly blocked MPP+-induced neuronal PC12D cell death and disappearance of mitochondrial membrane potential, which were mediated by JNK. |
| CFN92919 | Dauriporphinoline Dauriporphinoline is a natural product from Euchresta japonica. |
| CFN92920 | Menisporphine Menisporphine shows cytotoxic activity on the target cancer cell lines. It also shows significant angiogenesis inhibitions. |
| CFN92921 | Dauriporphine Dauriporphine shows cytotoxic activity on the target cancer cell lines, and shows significant angiogenesis inhibitions. Dauriporphine shows significant inhibitions on receptor activator of nuclear factor-κB ligand-induced differentiation of mouse bone marrow-derived macrophages into multinucleated osteoclasts. Dauriporphine shows potent P-gp MDR inhibition activity with an ED50 value 0.03 microg/mL and 0.00010 microg/mL in the MES-SA/DX5 and HCT15 cells, respectively. |
| CFN92922 | 22-beta-Acetoxyglycyrrhizin 22-beta-Acetoxyglycyrrhizin is a natural product from Glycyrrhiza uralensis. |
| CFN92923 | Licoricesaponin A3 Licoricesaponin A3 shows the cytotoxic activity against the human cancer cell lines MGC-803, SW620, and SMMC-7721 with IC50 > 100 μmol/L. |
| CFN92924 | Uralsaponin C Uralsaponin C shows the cytotoxic activity against the human cancer cell lines MGC-803, SW620, and SMMC-7721 with IC50 > 100 μmol/L. |
| CFN92925 | Isoliquiritoside Isoliquiritoside has antioxidant activity,remarkable anti-tumor and anti-HIV effects. It shows strong inhibition against pancreatic lipase ( IC50 of 37.6 uM ). |
| CFN92926 | Curryangine Reference standards. |
| CFN92927 | Murrayamine E Murrayamine E is a natural product from Murraya exotica. |
| CFN92928 | 1-vinyl-4-dimethoxy-beta-carboline 1-vinyl-4-dimethoxy-beta-carboline is a natural product from Picrasma javanica. |
| CFN92929 | 4-Hydroxy-1-methoxycarbonyl-beta-carboline Reference standards. |
| CFN92930 | 5-Hydroxy-canthin-6-one Reference standards. |
| CFN92931 | 1-Methoxymethyl-beta-carboline 1-Methoxymethyl-beta-carboline is a natural product from Picrasma javanica. |
| CFN92932 | 3,3'-Bilawsone 3,3'-Bilawsone is a natural product from Lomatia ferruginea. |
| CFN92933 | 1H-Pyrido[3,4-b]indole-1,3 4(2H,9H)-trione Reference standards. |
| CFN92934 | trans-Cinnamic anhydride trans-Cinnamic anhydride is a acylating agent. |
| CFN92935 | Spiranthesol Spiranthesol is a natural product from Spiranthes australis. |
| CFN92936 | Isophysalin A Isophysalin A exhibits anti-inflammatory activitiy, it exhibits conjugating abilities with glutathione and also shows significant nitric oxide (NO) production inhibiting activities. |
| CFN92937 | Physalin H Physalin H is an Hh signaling inhibitor blocks GLI1-DNA-complex formation, it also strong quinone reductase induction activity with IR (Induction ratio, QR induction activity) value of 3.74±0.02. Physalin H shows immunosuppressive effects on T cells both in vitro and in vivo, and the immunosuppressive activity might be attributed to the suppression of T cell activation and proliferation, the modulation of Th1/Th2 cytokine balance and the induction of HO-1 in T cells. Physalin H shows significant in vitro leishmanicidal activities (0.92-19.4 microg/ml) against promastigotes of Leishmania major.Physalin H shows cytotoxic activity against a panel of human and murine cancer cell lines. |
| CFN92938 | Physalin C Physalin C is a natural product from Physalis alkekengi. |
| CFN92939 | Physalin D Physalin D shows antimalarial activity; it also exhibits a minimum inhibitory concentration value (MIC) against Mycobacterium tuberculosis H(37)Rv strain of 32 microg/mL. Physalin D displays considerable cytotoxicity against several cancer cell lines. It presents antinociceptive properties associated with central. |
| CFN92940 | Physalin A Physalin A exerts anti-tumor activity in non-small cell lung cancer cell lines by suppressing JAK/STAT3 signaling, it inhibits androgen-independent prostate cancer cell growth through activation of cell apoptosis and downregulation of androgen receptor expression. Physalin A induces apoptosis via p53-Noxa-mediated ROS generation, and autophagy plays a protective role against apoptosis through p38-NF-κB survival pathway in A375-S2 cells. |
| CFN92941 | Physalin B Physalin B shows antimalarial, anti-Trypanosoma cruzi, anti-bacterial, anti- leukemia activities, it has the potential to be developed as an effective chemotherapeutic lead compound for the treatment of malignant melanoma, it inhibits androgen-independent prostate cancer cell growth through activation of cell apoptosis and downregulation of androgen receptor expression. Physalin B exhibits a minimum inhibitory concentration value (MIC) against Mycobacterium tuberculosis H(37)Rv strain of 32 microg/mL. Physalin B also presents antinociceptive properties associated with central. |
| CFN92942 | Xanthone V1a Reference standards. |
| CFN92943 | Minimolide F Minimolide F displays inhibitory activity against human nasopharyngeal cancer cells (CNE) with IC(50) values ranging from 1.1 to 20.3 uM. |
| CFN92944 | Thermopsidine Reference standards. |
| CFN92945 | Mogroside IIIe Mogroside IIIe has anti-inflammatory activity, it attenuates LPS-induced acute lung injury in mice partly through regulation of the TLR4/MAPK/NF-κB axis via AMPK activation. It also has anti-fibrotic activity, it reduces pulmonary fibrosis through Toll-Like receptor 4 pathways. |
| CFN92946 | Mogroside III-A2 Mogroside III-A2 exhibits inhibitory effects with IC50 values of 346-400 mol ratio/32 pmol TPA. and shows weak inhibitory effects on activation of (+/-)-(E)-methyl-2-[(E)-hydroxyimino]-5-nitro-6-methoxy-3-hexemide (NOR 1), a nitric oxide (NO) donor. |
| CFN92947 | Mogroside II-A1 Mogroside II-A1 exhibits inhibitory effects with IC50 values of 346-400 mol ratio/32 pmol TPA. and shows weak inhibitory effects on activation of (+/-)-(E)-methyl-2-[(E)-hydroxyimino]-5-nitro-6-methoxy-3-hexemide (NOR 1), a nitric oxide (NO) donor. |
| CFN92948 | Trilobinine (+)-Trilobinine has relaxant effects via the activation of beta 2-adrenoceptors, it can reduce the spontaneous tone and inhibit the contractions induced by carbachol and histamine. |
| CFN92949 | Caulophyllumine A Caulophyllumine A is a natural product from Cimicifuga heracleifolia. |
| CFN92950 | 5-O-Caffeoylshikimic acid 5-O-Caffeoylshikimic acid shows anti-oxidative activity; it also shows anti-inflammatory activity, the underlying mechanism was associated with downregulation of nuclear factor-κB. 5-O-Caffeoylshikimic acid can remarkably inhibit the macrophage migration and adhesion. It also shows moderate MDR reversal activity. |
| CFN92951 | 3-O-Caffeoylshikimic acid 3-O-Caffeoylshikimic acid shows anti-oxidative activity, it also shows potent antiproliferative activities with IC(50) values among 5-150 μM against HepG2 human liver cancer, HL-60 human myeloid leukemia, K562 human myeloid leukemia, and CNE-1 human nasopharyngeal carcinoma cell lines. |
| CFN92952 | 4-O-Caffeoylshikimic acid 4-O-Caffeoylshikimic acid is a natural product from Illicium verum. |
| CFN92953 | Leucanthogenin Reference standards. |
| CFN92954 | 5,7,4'-Trimethoxyafzelechin 5,7,4'-Trimethoxyafzelechin is a natural product from Celastrus orbiculatus. |
| CFN92955 | Isoatriplicolide tiglate Isoatriplicolide tiglate acts as an antiproliferation agents particularly against breast and cervical cancers by inducing cell cycle arrest in the S/G2 phase and caspase dependent apoptosis at relatively low (< 10 μg/mL) and high (> 50 μg/mL) concentrations, respectively. Isoatriplicolide tiglate exhibits significant neuroprotective activity against glutamate-induced toxicity at concentrations ranging from 1 uM to 10 uM. |
