| Catalog No | Product Description | CAS No. | Purity | Structural Formula |
|---|---|---|---|---|
| SBP02354 | 919769-83-8 |
|
||
| BP5524 | 84294-87-1 | 98% |
|
|
| 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% |
|
| SBP01167 | 27740-43-8 |
|
||
| SBP01238 | 28619-41-2 |
|
||
| SBP03248 | 80510-09-4 |
|
||
| BP5656 | 176182-06-2 |
|
||
| BPC0059 | 14773-42-3 |
|
||
| BP5012 | 34170-18-8 | 98% |
|
|
| SBP01947 | 62312-55-4 |
|
||
| BP3312 | 150881-01-9 |
|
||
| BP1456 | 212701-97-8 |
|
||
| BP3054 |
Adenosine
Adenosine is a nucleoside composed of a molecule of adenine attached to a ribose sugar molecule (ribofuranose) moiety via a β-N9-glycosidic bond. Adenosine induces SphK1 activity in human and mouse sickle and normal erythrocytes in vitro, it can activate the neuroimmune system, alter neuronal function and neurotransmission,and contribute to symptoms of sickness and psychopathologies. Adenosine activates mast cells have been long implicated in allergic asthma and studies in rodent mast cells have assigned the A3 Adenosine receptor (A3R) a primary role in mediating Adenosine responses. Adenosine is a ribonucleoside composed of a molecule of adenine attached to a ribofuranose moiety via a betaN9-glycosidic bond. It has a role as an analgesic, a vasodilator agent, an anti-arrhythmia drug, a human metabolite and a fundamental metabolite. It is a purines D-ribonucleoside and a member of adenosines. It is functionally related to an adenine.
|
58-61-7 | 98% |
|
| SBP01354 | 1467083-10-8 |
|
||
| BPC0229 | 75656-91-6 |
|
||
| BP2299 | 28251-63-0 | 98% |
|
|
| BP5773 | 116159-73-0 |
|
||
| BP1391 |
Thermopsine
Thermopsine exhibits antibacterial activity.
|
486-90-8 | 98% |
|
| BP0273 |
Bicuculline
Bicuculline is a benzylisoquinoline alkaloid that is 6-methyl-5,6,7,8-tetrahydro[1,3]dioxolo[4,5-g]isoquinoline which is substituted at the 5-pro-S position by a (6R)-8-oxo-6,8-dihydrofuro[3,4-e][1,3]benzodioxol-6-yl group. A light-sensitive competitive antagonist of GABAA receptors. It was originally identified in 1932 in plant alkaloid extracts and has been isolated from Dicentra cucullaria, Adlumia fungosa, Fumariaceae, and several Corydalis species. (+)-Bicuculline is a competitive antagonist of GABAA receptors with IC50 of 2 μM, also blocks Ca(2+)-activated potassium channels.It is effective in vitro against spore germination of some plant pathogenic fungi, it can significantly inhibit spore germination of all the fungi at concentrations of 100-1000 ppm.
|
485-49-4 | 98% |
|
| BPC0353 | 62018-77-3 |
|
Shenshuai
Wenjing
Hedandan