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Golgicide A
CAS No. 1139889-93-2
Golgicide A( —— )
Catalog No. M19453 CAS No. 1139889-93-2
Golgicide A is a potent and rapidly reversible GBF1 inhibitor.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 60 | In Stock |
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| 2MG | 34 | In Stock |
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| 5MG | 55 | In Stock |
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| 10MG | 93 | In Stock |
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| 25MG | 188 | In Stock |
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| 50MG | 305 | In Stock |
|
| 100MG | 492 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | 1051 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameGolgicide A
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NoteResearch use only, not for human use.
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Brief DescriptionGolgicide A is a potent and rapidly reversible GBF1 inhibitor.
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DescriptionGolgicide A is a potent highly specific and reversible inhibitor of the cis-Golgi ADP-ribosylation factor guanine nucleotide exchange factors (ArfGEF) GBF1. Golgicide A drastically reduced replication of coxsackievirus B3 (CVB3) and other human enterovirus species.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorGBF1
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Research Area——
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Indication——
Chemical Information
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CAS Number1139889-93-2
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Formula Weight284.3
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Molecular FormulaC17H14F2N2
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Purity>98% (HPLC)
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SolubilityDMSO:14.2 mg/mL (50 mM)
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SMILES[H][C@@]12CC=C[C@]1([H])C1=C(NC2C2=CN=CC=C2)C(F)=CC(F)=C1
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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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Apelin-12 (human, bo...
Apelin-12 is one of the most potent C-terminal fragments of the polypeptide that possesses a high affinity to orphan receptor APJ receptor. Apelin-12 is involved in the regulation of body fluid homeostasis and in the central control of feeding. Apelin-12 blocks HIV-1 entry through APJ receptor. Apelin-12 exerts neuroprotective effect.
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CDK2
CDK2 is a member of the eukaryotic S/T protein kinase family and its function is to catalyze the phosphoryl transfer of ATP γ-phosphate to serine or threonine hydroxyl (denoted as S0/T0) in a protein substrate.
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Thioredoxin reductas...
Thioredoxin reductase peptide corresponds to residues 53–67 in thioredoxin reductase (TrxR), used in thioredoxin reductase research.Mammalian thioredoxin reductase (TR) catalyzes the reduction of the redox-active disulfide bond of thioredoxin (Trx) and is similar in structure and mechanism to glutathione reductase except for a C-terminal 16-amino acid extension containing a rare vicinal selenylsulfide bond.
