KM-023
CAS No. 1097628-00-6
KM-023( —— )
Catalog No. M35996 CAS No. 1097628-00-6
KM-023 is a new second-generation non-nucleoside reverse transcriptase inhibitor for the study of human immunodeficiency virus (HIV) type 1 infection.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 358 | In Stock |
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| 5MG | 361 | In Stock |
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| 10MG | 542 | In Stock |
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| 25MG | 870 | In Stock |
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| 50MG | 1163 | In Stock |
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| 100MG | 1562 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | 3134 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameKM-023
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NoteResearch use only, not for human use.
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Brief DescriptionKM-023 is a new second-generation non-nucleoside reverse transcriptase inhibitor for the study of human immunodeficiency virus (HIV) type 1 infection.
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DescriptionKM-023 is a new second-generation non-nucleoside reverse transcriptase inhibitor for the study of human immunodeficiency virus (HIV) type 1 infection.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayMicrobiology/Virology
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TargetHIV
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RecptorHIV Protease
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Research Area——
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Indication——
Chemical Information
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CAS Number1097628-00-6
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Formula Weight325.36
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Molecular FormulaC18H19N3O3
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Purity>98% (HPLC)
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Solubility——
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SMILESC(=O)(C1=C(C(C)C)C(=O)NC(=O)N1CC)C2=CC(C#N)=CC(C)=C2
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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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14-Dicaffeoylquinic ...
14-Dicaffeoylquinic acid has antioxidant activity.14-Dicaffeoylquinic acid is a potent and highly selective class of HIV-1 integrase inhibitors inhibitsHIV-1 replication in MT-2 cell culture at non-toxic concentrations.
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HIV-IN-6
HIV-IN-6 is an HIV viral inhibitor that inhibits the replication of the HIV virus.HIV-IN-6 has anti-HIV viral activity and works by targeting Src family kinases (SFK) (e.g., Hck) that interact with the viral Nef protein.
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Cosalane
Cosalane (NSC 658586) is an HIV replication inhibitor, an inhibitor of chemokine receptor 7 (CCR7) signalling in humans and mice, with antiviral activity that blocks the binding of CCR7 to its natural ligands, CCL19 and CCL21.
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