| Catalog No | Product Description | CAS No. | Purity | Structural Formula |
|---|---|---|---|---|
| BP5346 |
Artesunate Peroxy Hemiacetal
Artesunate is a part of the artemisinin group of agents with an IC50 of < 5 μM for small cell lung carcinoma cell line H69. It is a potential inhibitor of STAT-3 and exhibits selective cytotoxicity of cancer cells over normal cells in vitro; A potent inhibitor of EXP1.Artesunate has anti-inflammatory activity, can prevent neuroinflammation in BV2 microglia by interfering with NF-κB and p38 MAPK signalling.
|
958447-25-1 | 98% |
|
| BP3922 |
Yadanziolide A
Yadanziolide A shows strong antiviral activity.
|
95258-14-3 | 98% |
|
| BP4757 | 51768-38-8 | 98% |
|
|
| BP1784 |
Eurycomanone
Eurycomanone has anti-cancer activity, it is cytotoxic on HepG2 cells by inducing apoptosis through the up-regulation of p53 and Bax, and down-regulation of Bcl-2.
|
84633-29-4 | 98% |
|
| SBP02579 | 1897-26-3 |
|
||
| BP3378 |
Taccalonolide A
Taccalonolide A is the first microtubule stabilizing agent to be discovered from a plant since identification of the mechanism of action of paclitaxel and it is the first natural product steroid identified to have these cellular effects.
|
108885-68-3 | 98% |
|
| SBP03207 | 464-85-7 |
|
||
| BP1730 |
Cratoxylone
1. Cratoxylone exhibits potent activity in vitro against Plasmodium falciparum chloroquine-resistant strain W2, with the IC₅₀ value belows 3 uM.
|
149155-01-1 | 98% |
|
| BP1425 |
Isopteropodine
Isopteropodine has antimicrobial activity, it shows strong apoptotic effects on acute leukaemic lymphoblasts, it also shows an ability to stimulate the immune system.
|
5171-37-9 | 98% |
|
| BP0809 |
Jatrorrhizine chloride
Jatrorrhizine has neuroprotective, antioxidative, anti-inflammatory, antihypercholesterolemic, and anti-hyperglycemia effects.Jatrorrhizine is expected to be developed as a new gastric prokinetic drug, it is metabolized by human CYP1A2 and multiple UGT1A isoforms. It has inhibitory activities against the expression of inducible NO syntase (iNOS) and cyclooxygenase-2 (COX-2), and can improve the utilization and excretion of cholesterol by up-regulating the mRNA and protein expression of LDLR and CYP7A1.
|
6681-15-8 | 98% |
|
| SBP02936 | 107633-69-2 |
|
||
| BP1795 | 138809-10-6 | 98% |
|
|
| SBP03208 | 59443-02-6 |
|
||
| BP0449 |
Daphnetin
Daphnetin is a dihydroxycoumarin that is being used in China for the treatment of coagulation disorders, is a protein kinase inhibitor, inhibits EGFR, PKA and PKC with IC50 of 7.67 μM, 9.33 μM and 25.01 μM, respectively, also known to exhibit antimalarial, anti-rheumatoid arthritis, anti-proliferative, anti-inflammatory and anti-oxidant activities. it is also a chelator and an antioxidant. Daphnetin can enhance immunological functions of B lymphocytes, the expression of IL-12 in B lymphocytes can be up-regulated by daphnetin through natural immunity approach.
|
486-35-1 | 99% |
|
| SBP03110 | 639-36-1 |
|
||
| BP0198 |
Artesunate
Artesunate is an artemisinin derivative that is the hemisuccinate ester of the lactol resulting from the reduction of the lactone carbonyl group of artemisinin. It is used, generally as the sodium salt, for the treatment of malaria. It has a role as a ferroptosis inducer, an antineoplastic agent and an antimalarial. It is a hemisuccinate, a sesquiterpenoid, a dicarboxylic acid monoester, a cyclic acetal, an artemisinin derivative and a semisynthetic derivative.
Artesunate is a part of the artemisinin group of agents with an IC50 of < 5 μM for small cell lung carcinoma cell line H69. It is a potential inhibitor of STAT-3 and exhibits selective cytotoxicity of cancer cells over normal cells in vitro; A potent inhibitor of EXP1.Artesunate has anti-inflammatory activity, can prevent neuroinflammation in BV2 microglia by interfering with NF-κB and p38 MAPK signalling.
Artesunate is an inhibitor of STAT-3 and export protein 1 (EXP1).
|
88495-63-0 | 98% |
|
| BP0196 |
Artemisic acid
artemisinic acid is a monocarboxylic acid that is prop-2-enoic acid which is substituted at position 2 by a 4,7-dimethyl-1,2,3,4,4a,5,6,8a-octahydronaphthalen-1-yl group (the 1S,4R,4aS,8aR diastereoisomer). It is a sesquiterpenoid precursor of artemisinin, obtained from sweet wormwood, Artemisia annua. It has a role as a metabolite. It is a member of octahydronaphthalenes, a monocarboxylic acid, a sesquiterpenoid and a carbobicyclic compound.
Artemisinic acid (Qing Hao acid) is a sesquiterpene that can be isolated from Artemisia annua L. and is also an important precursor for the synthesis of Artemisinin (HY-B0094). Artemisinic acid has various pharmacological activities, such as anti malarial activity, anti-tumor activity, antipyretic effect, antibacterial activity, allelopathic effect, and anti adipogenic effect.
|
80286-58-4 | 98% |
|
| BP0264 |
Febrifugine
Febrifugine is an effective coccidiostat, possesses schizonticide props; it and its derivatives shows high degree of antimalarial activity but use limited by toxicity .
|
24159-07-7 | 98% |
|
| SBP03261 | 464-86-8 |
|
||
| SBP03106 | 14103-09-4 |
|
Shenshuai
Wenjing
Hedandan