Cat. No. | Product Name | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
TN4642 | Neorauflavane
化合物 TN4642
|
53734-74-0 | 98% |
|
Neorauflavane shows tyrosinase inhibition, it can inhibit tyrosinase monophenolase activity with an IC50 of 30 nM, it also can efficiently reduce melanin content... | ||||
TN4580 | Morachalcone A
化合物 TN4580
|
76472-88-3 | 97.00% |
|
Morachalcone A displays significant tyrosinase inhibitory activity (IC50, 0.013 uM); it also exerts strong pancreatic lipase inhibition with IC 50 value of 6.2 u... | ||||
TC0017 | Haplopine
化合物 TC0017
|
5876-17-5 |
|
|
Haplopine shows photo-activated antimicrobial activity against S. aureus. It exhibits potent melanogenesis-inhibitory activities with almost no toxicity to the c... | ||||
TN1840 | Kurarinol
苦参醇
|
855746-98-4 | 98% |
|
Kurarinol is a potent inhibitor of sortase A, with an IC50 value of 107.7 ± 6.6 μM. Kurarinol has extremely strong tyrosinase inhibitory activity, exerts varying... | ||||
TN2672 | 2-(2,4-Dihydroxyphenyl)-6-hydroxybenzofuran
化合物 TN2672
|
67736-22-5 | 98% |
|
2-(2,4-Dihydroxyphenyl)-6-hydroxybenzofuran shows radical scavenging activities. It also shows mushroom tyrosinase inhibitory activity with an IC50 value of 5.2 ... | ||||
T37961 | P-Tolualdehyde
对甲苯醛
|
104-87-0 | 98% |
|
p-Tolualdehyde 是一种 RIFM 香料,对蘑菇酪氨酸酶显示出抑制作用。 | ||||
T79401 | Tyrosinase-IN-13
化合物 Tyrosinase-IN-13
|
98% |
|
|
Tyrosinase-IN-13 (compound 3c)为Flurbiprofen的衍生物,具有非竞争性酪氨酸酶抑制活性(IC50=68 μM;Ki=36.3 μM),并对肝细胞癌(HepG2)、结直肠癌(HT-29)及黑色素瘤(B16F10)细胞表现出细胞毒性。 | ||||
T79406 | Tyrosinase-IN-14
化合物 Tyrosinase-IN-14
|
98% |
|
|
Tyrosinase-IN-14 (compound 7m) 是一种针对酪氨酸酶的抑制剂, 它通过改变酪氨酸酶的二级结构来降低其催化活性。此化合物的细胞毒性较低, 并且在水果抗褐变方面显示出活性。特别是,Tyrosinase-IN-14 在抑制香蕉储藏期间的褐变方面表现出了有效性。 | ||||
T80203 | Diaminopropionoyl tripeptide-33
化合物 Diaminopropionoyl tripeptide-33
|
1199495-15-2 | 98% |
|
Diaminopropionoyl tripeptide-33为生物活性肽,能保护皮肤细胞不受UVA引发的DNA损伤,已报道在化妆品成分中应用。 | ||||
T80909 | Tyrosinase-IN-19
化合物 Tyrosinase-IN-19
|
98% |
|
|
Tyrosinase-IN-19 是竞争性酪氨酸酶抑制剂,对ROS、ABTS+ 及DPPH 自由基展现显著的抗氧化活性。该化合物通过剂量依赖性方式有效抑制酪氨酸酶表达。 | ||||
T80910 | Tyrosinase-IN-15
化合物 Tyrosinase-IN-15
|
98% |
|
|
Tyrosinase-IN-15 (Compound 39)为酪氨酸酶抑制剂,具有IC50值为7.12 μM及Ki值为11.8 μM。 | ||||
TN5117 | Taxiphyllin
化合物 TN5117
|
21401-21-8 | 98% |
|
Taxiphyllin can inhibit tyrosinase activity in vitro significantly and is a potent tyrosinase inhibitor. Taxiphyllin displays mild antibacterial activity against... | ||||
TN3540 | Broussonin C
化合物 TN3540
|
76045-49-3 | 98% |
|
Broussonin C and broussin are antifungal compounds. Broussonin C exerts simple reversible slow-binding inhibition against diphenolase. | ||||
TN2303 | Viscumneoside III
槲寄生新苷III
|
118985-27-6 | 98% |
|
Viscumneoside III 是一种二氢黄酮 O-糖苷,抑制酪氨酸酶 (tyrosinase),IC50 为 0.5 mM。Viscumneoside III 具有抗心绞痛作用。 | ||||
TN3644 | Chlorophorin
化合物 TN3644
|
537-41-7 | 98% |
|
Chlorophorin shows high anti-protozoal activity with an MIC of 0.25 microg/ml. Chlorophorin can strongly inhibit mushroom tyrosinase activity with IC50 values of... | ||||
TN2288 | Uralenol
化合物 TN2288
|
139163-15-8 | 98% |
|
Uralenol significantly shows the inhibitory activities against the PTP1B enzyme; it also shows inhibitory activities on mushroom tyrosinase using l-tyrosine as s... | ||||
TN2280 | Trametenolic acid
3-羟基羊毛甾-8,24-二烯-21-酸
|
24160-36-9 | 98% |
|
Trametenolic acid is a cytotoxic agent.It exhibits a mode of mixed inhibition with a K I of 0.9μM, K IS of 0.5μM, and an IC50 of 7.25μM.Trametenolic acid and Bet... | ||||
TN1314 | 6-Hydroxykaempferol
6-羟基山奈酚
|
4324-55-4 | 98% |
|
6-Hydroxykaempferol is a competitive inhibitor of tyrosinase compared to L-DOPA, it shows also high antioxidant activities. | ||||
T2S0799 | Noroxyhydrastinine
化合物 T2S0799
|
21796-14-5 | 98% |
|
Noroxyhydrastinine exhibits potent melanogenesis-inhibitory activities, it inhibits melanogenesis, at least in part, by inhibiting the expression of protein leve... | ||||
T10664 | Calcium 2-oxoglutarate
化合物 T10664
|
71686-01-6 | 98% |
|
Calcium 2-oxoglutarate is an intermediate in the production of GTP or ATP in the Krebs cycle. It is a reversible inhibitor of tyrosinase (IC50: 15 mM). |