Procyanidin A1
CAS No. 103883-03-0
Procyanidin A1( Proanthocyanidin A1 )
Catalog No. M23247 CAS No. 103883-03-0
Procyanidin A1 has antiallergic effects, it inhibits degranulation downstream of protein kinase C activation or Ca2+; influx from an internal store in RBL-2H3 cells.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 188 | In Stock |
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| 5MG | 155 | In Stock |
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| 10MG | 250 | In Stock |
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| 25MG | 424 | In Stock |
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| 50MG | 600 | In Stock |
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| 100MG | Get Quote | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameProcyanidin A1
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NoteResearch use only, not for human use.
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Brief DescriptionProcyanidin A1 has antiallergic effects, it inhibits degranulation downstream of protein kinase C activation or Ca2+; influx from an internal store in RBL-2H3 cells.
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DescriptionProcyanidin A1 has antiallergic effects, it inhibits degranulation downstream of protein kinase C activation or Ca2+; influx from an internal store in RBL-2H3 cells.
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In Vitro——
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In Vivo——
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SynonymsProanthocyanidin A1
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PathwayGPCR/G Protein
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TargetCalcium Channel
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RecptorCalcium Channel|LDL|PKC
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Research Area——
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Indication——
Chemical Information
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CAS Number103883-03-0
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Formula Weight576.5
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Molecular FormulaC30H24O12
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (173.46 mM)
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SMILESO[C@@H](C1)[C@@H](c(cc2)cc(O)c2O)Oc2c1c(O)cc1c2[C@H]([C@@H]2O)c(c(O)cc(O)c3)c3O[C@@]2(c(cc2)cc(O)c2O)O1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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L-Phenylalanine-15N
L-Phenylalanine-15N ((S)-2-Amino-3-phenylpropionic acid-15N) is the 15N-labeled L-Phenylalanine. L-Phenylalanine ((S)-2-Amino-3-phenylpropionic acid) is an essential amino acid isolated from Escherichia coli . L-Phenylalanine is a α2δ subunit of voltage-dependent Ca + channels antagonist with a K i of 980 nM.
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Ticolubant
Ticolubant is orally active leukotriene B4 antagonist with high affinity for the human neutrophil LTB4 receptor (Ki = 0.78 nM), blocks LTB4-induced Ca2+ migration with an IC50 of 6.6 ± 1.5 nM, and shows topical anti-inflammatory activity in a mouse model of skin inflammation.
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Stugeron
Cinnarizine is a drug derivative of piperazine, and characterized as an antihistamine and a calcium channel blocker.
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