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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Curcumin | 458-37-7 | sc-200509 sc-200509A sc-200509B sc-200509C sc-200509D sc-200509F sc-200509E | 1 g 5 g 25 g 100 g 250 g 1 kg 2.5 kg | $36.00 $68.00 $107.00 $214.00 $234.00 $862.00 $1968.00 | 47 | |
Curcumin is a yellow-orange dye, NOS2 regulator, and inhibitor of NF-κB, 5-LO, Cox-2, COP9, and p300/CBP. | ||||||
N-Acetyl-L-tyrosinamide | 1948-71-6 | sc-301273 sc-301273A | 1 g 5 g | $97.00 $255.00 | ||
N-Acetyl-L-tyrosinamide is an analogue of L-tyrosine which stimulates the transport of L-Tyr, mainly by the ASC system | ||||||
GSK 4716 | 101574-65-6 | sc-203986 sc-203986A | 10 mg 50 mg | $71.00 $285.00 | ||
GSK 4716 is a selective agonist with estrogen-related receptors ERRβ and ERRγ | ||||||
Tyrphostin 51 | 122520-90-5 | sc-200545 sc-200545A | 5 mg 25 mg | $59.00 $305.00 | ||
Tyrphostin 51 is a potent inhibitor of EGFRK activity showing mixed competitive inhibition with ATP and substrate1-3. | ||||||
N-[3-(4-hydroxyphenyl)-1-oxo-2-propenyl]-L-phenylalanine, methyl ester | 615264-52-3 | sc-221976 sc-221976A | 5 mg 10 mg | $45.00 $87.00 | 1 | |
N-[3-(4-hydroxyphenyl)-1-oxo-2-propenyl]-L-phenylalanine, methyl ester is an inhibitor of ACAT-1 and -2 | ||||||
AMI-1, free acid | 134-47-4 | sc-300192 | 1 g | $96.00 | ||
AMI-1, free acid is a chemical shown to inhibit arginine, in vitro, with no inhibitory effect on lysine | ||||||
Butein | 487-52-5 | sc-202510 sc-202510A | 5 mg 50 mg | $172.00 $306.00 | 8 | |
Butein is inhibits the tyrosine kinase activity of the EGF receptor and p60c-src | ||||||
γ-Tocotrienol | 14101-61-2 | sc-205529 sc-205529A | 1 mg 10 mg | $48.00 $349.00 | 2 | |
γ-Tocotrienol is an antioxidant | ||||||
cis-Resveratrol Solution (in Ethanol) | 61434-67-1 | sc-205254 sc-205254A | 5 mg 10 mg | $120.00 $228.00 | 2 | |
cis-Resveratrol Solution (in Ethanol) is an antioxidant antiproliferative compound shown to inhibit Cox-1 | ||||||
SKF 38393 hydrochloride | 62717-42-4 | sc-203264 | 25 mg | $49.00 | ||
SKF 38393 hydrochloride is a benzazepine selective agonist of D1DR |