Products with
Precursors bioactivity
Cat.No.
|
Product Name
|
BCN1424 |
Hordenine
|
Hordenine is an inhibitor of noradrenaline uptake, is also an effective inhibitor of hyperpigmentation. It can inhibit melanogenesis by suppressing cAMP production, which is involved in the expression of melanogenesis-related proteins. Hordenine also has a positive inotropic effect upon the heart, increases systolic and diastolic blood pressure, peripheral blood flow volume, inhibits gut movements. |
BCN1475 |
1,2:4,5-Di-O-isopropylidene-beta-D-fructopyranose
|
1. 1,2:4,5-di-O-isopropylidene-beta-D-fructopyranose is a synthetic precursor of the asymmetric epoxidation catalyst 1,2:4,5-di-O-isopropylidene-beta-D-erythro-2,3-
hexadiulo-2,6-pyranose. |
BCN1544 |
5'-Deoxy-5-fluoro-N-[(pentyloxy)carbonyl]cytidine 2',3'-diacetate
|
1. 5'-Deoxy-5-fluoro-N-[(pentyloxy)carbonyl]cytidine 2',3'-diacetate,which is a key intermediate of capecitabine. |
BCN1749 |
Hypotaurine
|
1. Hypotaurine is a precursor of taurine and an antioxidant, intracellular hypotaurine is mainly supplied to placental trophoblasts by transfer from extracellular fluid across the plasma membrane, and may play a role in cell protection by scavenging reactive oxygen species.
2. Hypotaurine and cysteine sulfinate have scavenging activity towards the carbonate radical anion.
3. Hypotaurine/taurine synthesis strongly inhibits cysteinesulfinate decarboxylase (pyridoxal 5'-phosphate-dependent enzyme) as well as cystathionine γ-lyase.
4. Hypotaurine and raffinose supplementation in semen extenders provide a protection of sperm parameters against cryopreservation injury.
5. Hypotaurine suppresses acute, inflammatory, and neuropathic pain, may regulate nociceptive transmission physiologically by activating glycinergic neurons in the spinal cord, is a promising candidate for treating various pain states. |
BCN1778 |
8-Amino-7-oxononanoic acid
|
1. 8-Amino-7-oxononanoic acid is a precursor of 7,8-Diaminopelargonic acid (DAPA), and 7,8-diaminopelargonic acid aminotransferase (DAPA AT) is a potential drug target in Mycobacterium tuberculosis. |