NS1-IN-1

SKU:BHB21900923
Research Validated
Overview
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NS1-IN-1 (CAS 181373-35-3) is an inhibitor. Relevant to Anti-infection and PI3K/Akt/mTOR research. Molecular formula C23H26N2O4, molecular weight 394.46 g/mol. Also known as REDD1 inducer-1.
CAS Number 181373-35-3
Molecular Weight 394.46 g/mol
Storage See Certificate of Analysis
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Catalog no. Size
HY-134922-1MG 1 mg
HY-134922-5MG 5 mg
HY-134922-10MG 10 mg
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  • Options: Size: 1 mg, 5 mg, 10 mg
  • Lead time: made to order; typically ships within 2–3 weeks.
  • Storage: Please store the product under the recommended conditions in the Certificate of Analysis.
  • Shipping: Room temperature in continental US; may vary elsewhere.
  • Upon receipt: store as stated on the Certificate of Analysis; contact us if you need the condition before ordering.
Field Specification
Alternative names REDD1 inducer-1
CAS no. 181373-35-3
Applications
  • Functional Assay (In Vitro)
Molecular weight 394.46
Molecular formula C23H26N2O4
SMILES O=C(O)CCCCCN(C(C1=CC=C(N2CCCCC2)C3=CC=CC4=C13)=O)C4=O
Storage Refer to Certificate of Analysis (CoA) for storage conditions
Shipping Room temperature in continental US; may vary elsewhere.
Catalog no. (Mfr.) HY-134922
Main SKU BHB21900923
Inhibitors

Compound Overview

NS1-IN-1, also known as REDD1 inducer-1, is a naphthalimide compound and an NS1 inhibitor. It antagonizes influenza A virus NS1-mediated inhibition of host gene expression, induces REDD1 expression, and suppresses the mTORC1 signaling pathway via a TSC1-TSC2-dependent mechanism. It exhibits broad antiviral activity against influenza virus and vesicular stomatitis virus (VSV), with low toxicity[1]. It has the molecular formula C23H26N2O4 and a molecular weight of 394.46 g/mol.

Physical & Chemical Properties

CAS Number 181373-35-3
Molecular Formula C23H26N2O4
Molecular Weight 394.46 g/mol
SMILES O=C(O)CCCCCN(C(C1=CC=C(N2CCCCC2)C3=CC=CC4=C13)=O)C4=O
Signaling Pathway Anti-infection; PI3K/Akt/mTOR
Storage Please store the product under the recommended conditions in the Certificate of Analysis.
Shipping Room temperature in continental US; may vary elsewhere.

Literature Cited

Sources cited in this description and in the In Vitro & In Vivo Data tab. Peer-reviewed publications that used this product are listed under References.

[1]. Mata MA, et al. Chemical inhibition of RNA viruses reveals REDD1 as a host defense factor. Nat Chem Biol. 2011 Sep 11;7(10):712-9.

Safety

For Research Use Only. Not for use in diagnostic or therapeutic procedures, and not for human or veterinary use. Handle in accordance with your institution's chemical hygiene plan.

In Vitro

NS1-IN-1 (25-50 μM; 24-30 h) decreases replication of influenza virus and expression of viral proteins (NP, M1, etc.) in MDCK cells while showing low cytotoxicity, in line with a cell viability assay giving CC50/IC50 ≈ 31[1]. In A549 cells, NS1-IN-1 (30 μM; 4-9 h) inhibits influenza viral protein expression and induces REDD1, while suppressing mTORC1 signaling through a TSC1-TSC2 dependent mechanism[1]. NS1-IN-1 (30 μM; up to 18 h) induces REDD1 mRNA transcriptionally without activating IFN-β or ISGs, confirming an interferon-independent antiviral mechanism[1]. NS1-IN-1 (25-50 μM; 24 h) additionally blocks VSV infection in MDCK cells, with antiviral activity depends on the REDD1-TSC1-TSC2-mTORC1 axis[1].

Cell Viability Assay[1]

Cell LineMDCK, MEF, HBEC cells
Concentration0.2-100 μM
Incubation Time24-72 h
ResultShowed low cytotoxicity in host cells, with CC50/IC50 selectivity ratio of approximately 31.

Western Blot Analysis[1]

Cell LineMDCK, A549 cells
Concentration30 μM
Incubation Time4-9 h post-infection
ResultDownregulated influenza viral proteins (NS1, NP, M1, etc.) and induced REDD1 protein (6-8 fold). Reduced S6K phosphorylation at Thr389 (mTORC1 inhibition) without directly affecting AKT in early stages.

Real Time qPCR[1]

Cell LineA549 cell
Concentration30 μM
Incubation TimeVarious time points (up to 18 h pretreatment + infection)
ResultTranscriptionally induced REDD1 mRNA expression; induction was abolished by actinomycin D. Did not induce IFN-β or interferon-stimulated genes.

Data provided by the manufacturer. Numbered citations refer to the Literature Cited list in the product description.

Q.How long does this take to ship?
A.This item is produced on request and typically ships within 2–3 weeks.
Q.Can this be used in humans or for diagnostics?
A.No. This product is supplied For Research Use Only. It is not for diagnostic or therapeutic procedures and not for human or veterinary use.

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Microglial SIRT1 activation attenuates synapse loss in retinal inner plexiform layer via mTORC1 inhibition. J Neuroinflammation 2023 Sep 5;20(1):202. PMID: 37670386

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