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CHS3

Catalog No Product Description CAS No. Purity Structural Formula
BPC0148
Anisodine
Anisodine is a traditional anticholinergics, it and anisodamine possess alpha 1-adrenoceptor blocking properties, they are widely used in the People's Republic of China for the management of acute circulatory shock . Anisodine can protect optic nerve of primary open angle glaucoma (POAG) through improving the visual function and blood supply of optic nerve. The combination of Anisodine and citicoline with standard steroid and mannitol therapy appears to be effective in the treatment of early optic nerve contusion.
52646-92-1 98% Anisodine
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% Eurycomanone
BP1795 138809-10-6 98% 13-alpha-(21)-Epoxyeurycomanone
BP3029
4-Methoxysalicylaldehyde
2-Hydroxy-4-methoxybenzaldehyde is a member of phenols and a member of methoxybenzenes.
673-22-3 98% 4-Methoxysalicylaldehyde
BP4932
Sterebin E
Sterebin E may have anti-inflammatory activity.
114343-74-7 98% Sterebin E
BP3527
L-Cysteine hydrochloride monohydrate
L-Cysteine inhibits insulin release via multiple actions on the insulin secretory process through H(2)S production. L-Cysteine administration limits ischemia-reperfusion injury through a mechanism that appears to be at least partially dependent on H2S synthesis. L-cysteine hydrochloride hydrate is a hydrate that is the monohydrate form of L-cysteine hydrochloride. It has a role as a flour treatment agent, an EC 4.3.1.3 (histidine ammonia-lyase) inhibitor and a human metabolite. It contains a L-cysteine hydrochloride.
7048-04-6 98% L-Cysteine hydrochloride monohydrate
BP4822
Cichorin
Cichoriin is a member of coumarins and a glycoside.
531-58-8 98% Cichorin
BP3540
L-Aspartic acid
L-aspartic acid is the L-enantiomer of aspartic acid. It has a role as a neurotransmitter, a mouse metabolite and an Escherichia coli metabolite. It is a L-alpha-amino acid, an aspartate family amino acid, an aspartic acid and a proteinogenic amino acid. It is a conjugate acid of a L-aspartate(1-). It is an enantiomer of a D-aspartic acid. L-Aspartic acid induces a region of negative slope conductance in the current-voltage relationship of cultured spinal cord neurons. It could as the amino donor.
56-84-8 L-Aspartic acid
BP1459
Xanthotoxol
Xanthotoxol shows strong pharmacological activities as anti-inflammatory, antioxidant, cytotoxic, dose-graded sedative, 5-HT antagonistic, and neuroprotective effects.Xanthotoxol also has calcium antagonistic effects, it blocks not only the voltage dependent calcium channel, but also the receptor operated calcium channel in the isolated guinea pig atria.
2009-24-7 98% Xanthotoxol