| Catalog No | Product Description | CAS No. | Purity | Structural Formula |
|---|---|---|---|---|
| BP2242 | 26241-63-4 | 98% |
|
|
| BP3240 |
Lucidenic acid C
Lucidenic acid C has anti-invasive effect, it shows significant inhibitory effects on PMA-induced MMP-9 activity and invasion of HepG(2 )cells.
|
95311-96-9 | 98% |
|
| BP0002 | 116064-77-8 | 98% |
|
|
| BP1767 |
Magnocurarine
Magnocurarine is a natural product from Magnolia officinalis.
|
6801-40-7 | 98% |
|
| BP3633 |
Balanophonin, (+)-
Balanophonin shows potent α-glucosidase inhibitory activity, it has antioxidant, and anti-cancer activities. (±)-Balanophonin shows significant antibacterial activity against cariogenic oral streptococci, Streptococcus mutans and S. sobrinus.
|
215319-47-4 | 98% |
|
| BP5411 | 33458-84-3 | 98% |
|
|
| BP0333 |
Cephalotaxine
Cephalotaxine is a benzazepine alkaloid isolated from Cephalotaxus harringtonia. It is a secondary alcohol, an organic heteropentacyclic compound, a benzazepine alkaloid, a benzazepine alkaloid fundamental parent, an enol ether, a tertiary amino compound and a cyclic acetal. Cephalotaxine is an antiviral as well as antitumor agent. It is useless for the treatment of infection by flaviviruses, but potentially useful in combined therapy against hepatitis B.
|
24316-19-6 | 98% |
|
| BP1439 |
Vincristine
Vincristine-induced nociceptive painful sensation, may be due to its potential of antioxidative, neuroprotective and calcium channel inhibitory action.Vincristine can treat MM, ERK1/2, Akt, and NF-κB inhibitors are potentially useful as anti-MDR agents for the treatment of Vincristine-resistant MM. An inherited polymorphism in the promoter region of CEP72 was associated with increased risk and severity of Vincristine-related peripheral neuropathy. Vincristine is a vinca alkaloid with formula C46H56N4O10 found in the Madagascar periwinkle, Catharanthus roseus. It is used (commonly as the corresponding sulfate salt)as a chemotherapy drug for the treatment of leukaemia, lymphoma, myeloma, breast cancer and head and neck cancer. It has a role as a drug, an antineoplastic agent, a tubulin modulator, a microtubule-destabilising agent and a plant metabolite.
|
57-22-7 | 98% |
|
| BP2215 |
Ganoderic acid Gama
Ganoderic acid gamma is a triterpenoid.
|
294674-00-3 | 98% |
|
| BP2247 | 2226858-23-5 | 98% |
|
|
| BP1620 | 19716-59-7 | 98% |
|
|
| BP2197 | 562-35-6 | 98% |
|
|
| BP2170 |
Ganosporeric acid A
Ganosporeric acid A is a triterpenoid.
|
135357-25-4 | 98% |
|
| BP1720 |
Polyporenic acid C
Polyporenic acid C shows inhibitory activity against human collagenase. Polyporenic acid C induces apoptosis through the death receptor-mediated apoptotic pathway where the activation of caspase-8 leads to the direct cleavage of execution caspases without the involvement of the mitochondria.
|
465-18-9 | 98% |
|
| BP1658 |
Veratramine
Veratramine exhibits cytotoxic activity against human tumor cell lines A549, PANC-1, SW1990 and NCI-H249. Veratramine shows hypotensive effect, the effect is directly positively correlated with the dosage. Veratramine is a piperidine alkaloid comprising the 14,15,16,17-tetradehydro derivative of veratraman having two hydroxy groups at the 3- and 23-positions. It derives from a hydride of a veratraman.
|
60-70-8 | 98% |
|
| BP5401 | 244230-20-4 | 94% |
|
|
| SBP02410 | 139101-67-0 |
|
||
| BP3200 |
Hypaphorine
Hypaphorine is an amino acid betaine obtaine by exhaustive methylation of the alpha-amino group of L-tryptophan with concomitant deprotonation of the carboxy group. It has a role as a xenobiotic, a plant metabolite and a fungal metabolite. It is an amino-acid betaine, an indole alkaloid and a L-tryptophan derivative. Hypaphorine is an indole-3-acetic acid antagonist which specifically compete with indole-3-acetic acid in binding to the indole-3-acetic acid-binding site in plant peroxidases.Hypaphorine and endogenous indole-3-acetic acid counteract in controlling root hair elongation.
|
487-58-1 | 98% |
|
| BP3729 |
Etoposide
Etoposide is a beta-D-glucoside, an organic heterotetracyclic compound and a furonaphthodioxole. It has a role as an antineoplastic agent and a DNA synthesis inhibitor. It is functionally related to a podophyllotoxin and a 4'-demethylepipodophyllotoxin. Etoposide is a chemotherapy medication used for the treatments of a number of types of cancer. Etoposide inhibits DNA synthesis by forming a complex with topoisomerase II and DNA, it induces apoptosis in MCF-7 breast cancer cells.
|
33419-42-0 | 98% |
|
| BP1863 |
Epinodosin
Epinodosin induces significant DNA damage to HepG2 cells in a time- and dose-dependent manner.Epinodosin has a biphasic, dose-dependent effect on root growth and a strong inhibitory effect on root hair development in Lactuca sativa L. seedlings.
|
20086-60-6 | 98% |
|
Shenshuai
Wenjing
Hedandan