(-)-JNJ-A07
CAS No. 2135640-92-3
(-)-JNJ-A07( —— )
Catalog No. M35763 CAS No. 2135640-92-3
(-)-JNJ-A07 is a selective and potent dengue virus (DENV) inhibitor with an EC50 of 31 nM, exhibiting significant antiviral activity for the study of dengue virus infections.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 501 | In Stock |
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| 5MG | 392 | In Stock |
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| 10MG | 655 | In Stock |
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| 25MG | 1264 | In Stock |
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| 50MG | 1655 | In Stock |
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| 100MG | 2260 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product Name(-)-JNJ-A07
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NoteResearch use only, not for human use.
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Brief Description(-)-JNJ-A07 is a selective and potent dengue virus (DENV) inhibitor with an EC50 of 31 nM, exhibiting significant antiviral activity for the study of dengue virus infections.
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Description(-)-JNJ-A07 is a potent and selective DENV inhibitor with an EC50 value of 31 nM.
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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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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number2135640-92-3
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Formula Weight578.96
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Molecular FormulaC28H26ClF3N2O6
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (172.72 mM; Ultrasonic )
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SMILESC(C(NC1=CC(OCCCC(O)=O)=CC(OC)=C1)C2=CC=C(Cl)C=C2)(=O)N3C=4C(CC3)=CC=C(OC(F)(F)F)C4
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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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β-CGRP, human
β-CGRP, human ,a 37-amino acid peptide,is the beta form of Calcitonin-gene-related peptide (β-CGRP), involved extensively in regulation of the cardiovascular and nervous systems. β-CGRP contains a disulphide bridge at the N-terminus, a C-terminal phenylalanine amide important for immune recognition, and an a-helix between residues 8 and 18.
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Acid Yellow 36
Acid Yellow 36 is an azo dye and a pH indicator. Acid Yellow 36 changes its color from red at pH 1.2 to yellow at pH 2.3.
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Substance P (6-11)/H...
Substance P (6-11) is the C-terminal hexapeptideamide of Substance P (Substance P ).Substance P (6-11) binds to NK-1 tachykinin receptor. Substance P (6-11) shows depolarization of motoneurons and a hypotensive effect.
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