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Melanoma

Melanoma is a serious form of skin cancer that develops in melanocytes, the cells that produce melanin. It is often caused by exposure to ultraviolet (UV) radiation from sunlight or tanning beds. While less common than other skin cancers, melanoma is more dangerous due to its potential to metastasize rapidly if not detected and treated early. Early signs include changes in existing moles or the appearance of new, unusual-looking growths. Diagnosis typically involves a biopsy, and treatment options vary based on stage, including surgical excision, immunotherapy, targeted therapy, or chemotherapy.
Catalog No Product Description CAS No. Purity Structural Formula
BP2399 698393-97-4 98% 6-O-cinnamoyl-D-glucopyranose
BP5408 136172-60-6 98% 6'-O-Caffeoylarbutin
BP1323
Solasonine
Solasonine displays leishmanicidal activity against promastigote forms of L. amazonensis. Solasonine is a steroid, an azaspiro compound and an oxaspiro compound.
19121-58-5 98% Solasonine
BP1669
Fuscaxanthone C
1-Hydroxy-3,6,7-trimethoxy-2,8-diprenylxanthone is a member of xanthones. Fuscaxanthone C is a natural product from Garcinia mangostana.
15404-76-9 98% Fuscaxanthone C
BP4393
Lirinidine
(+)-Lirinidine has antioxidative activity, and it can significantly inhibit the proliferation of melanoma cells; it also shows potent inhibition of melanogenesis. Lirinidine exhibits significant inhibition of collagen, arachidonic acid and platelet activating factor-induced platelet aggregation.
54383-28-7 98% Lirinidine
BP1473
Ginsenoside RK2
Ginsenoside Rk1 has anti-tumor, and anti-platelet aggregation activities. Ginsenoside Rk1 can strongly inhibit permeability induced by VEGF, advance glycation end-product, thrombin, or histamine in human retinal endothelial cells, it reduces the vessel leakiness of retina in a diabetic mouse model; this anti-permeability activity of Rk1 is correlated with enhanced stability and positioning of tight junction proteins at the boundary between cells; Rk1 induces phosphorylation of myosin light chain and cortactin, which are critical regulators for the formation of the cortical actin ring structure and endothelial barrier.
364779-14-6 98% Ginsenoside RK2
BP5258
(+)-Rhododendrol
Rhododendrol is an inhibitor of melanin synthesis developed for lightening/whitening cosmetics, it can competitively inhibit mushroom tyrosinase and serve as a good substrate, while it also shows cytotoxicity against cultured human melanocytes at high concentrations sufficient for inhibiting tyrosinase. (+)-Rhododendrol and epi-rhododendrin have anti-inflammatory effect, they can suppress the NO production by activated macrophages in vivo.
59092-94-3 98% (+)-Rhododendrol
BP3256
Methyl rosmarinate
Methyl rosmarinate shows antioxidative, and antifungal activities. It has inhibitory activities against tyrosinase, α-glucosidase, and matrix metalloproteinase-1 (MMP-1).
99353-00-1 98% Methyl rosmarinate
BP0033
Inulicin
Inulicin is a terpene lactone.
33627-41-7 98% Inulicin
BP5335
Bruceoside A
Bruceoside A could be transformed into the potent anticancer component brusatol in vivo, rather than its direct deglycosylated metabolite bruceosin. It significantly inhibited P-388 lymphocytic leukemic cell RNA and protein synthesis in tissue culture.
63306-30-9 98% Bruceoside A
BP1665 87075-18-1 98% Isolindleyin
BP4388
Piperlonguminine
Piperlonguminine is an efficient depigmenting agent with a novel mechanism of action. It has potent antitumor, antitrypanosomal, anti-hyperlipidemic, anti-platelet and anti-melanogenesis activities. Piperlonguminine obviously improves hepatocyte fatty degeneration of alcoholic fatty liver in mice, it can effectively prevent the occurrence and development of alcoholic fatty liver. (E,E)-Piperlonguminine is a member of benzodioxoles.
5950-12-9 98% Piperlonguminine
BP2318
p-Coumaric acid 4-O-β-D-glucopyranoside
4-O-beta-D-glucosyl-trans-4-coumaric acid is a 4-O-beta-D-glucosyl-4-coumaric acid in which the double bond has trans-configuration. It has a role as a plant metabolite. It is a conjugate acid of a 4-O-beta-D-glucosyl-trans-4-coumarate.
117405-49-9 98% p-Coumaric acid 4-O-β-D-glucopyranoside
BP1254 5578-73-4 98% Sanguinarium chloride
BP0961
Morusin
Morusin is an extended flavonoid that is flavone substituted by hydroxy groups at positions 5, 2' and 4', a prenyl group at position 3 and a 2,2-dimethyl pyran group across positions 7 and 8. It has a role as an antineoplastic agent and a plant metabolite. It is a trihydroxyflavone and an extended flavonoid. Morusin exhibits antinociceptive, analgesic, anticonvulsant, antibacterial, and antitumor activities. Morusin can inhibit NF-κB and STAT3 activity, activate caspases activity, and restorate GABA level.
62596-29-6 98% Morusin
SBP03339 51095-47-7 Methyl p-hydroxyphenyllactate
BP5613 97653-92-4 Lucidone A
BP3045 842-01-3 7,8-Dihydroxy-4-phenylcoumarin
BP1467
Ziyuglycoside I
Ziyuglycoside I has anti-wrinkle activity, could be used as an active ingredient for cosmetics.
35286-58-9 98% Ziyuglycoside I
BP1657
Panaxydol
Panaxydol has anti-cancer activity, can inhibit the growth and apoptosis of cancer cells, the signaling mechanisms involve a [Ca(2+)](i) increase, JNK and p38 MAPK activation, cAMP, MAP kinase and ROS generation through NADPH oxidase and mitochondria. It induces the differentiation in C6 cells, may through a PI 3-K-dependent pathway. Panaxydol is a natural product found in Panax ginseng. It is an epoxide, an acetylenic compound and an olefinic compound.
72800-72-7 Panaxydol