Art. -Nr.: HY-170621

STAT1/3-IN-1

2 Cited Publications

Kundenbewertung

Based on 2 publication(s) in Google Scholar

STAT1/3-IN-1 is a potent STAT1/3 inhibitor with potent anti-inflammatory effect. STAT1/3-IN-1 inhibits phosphorylation and nuclear translocation of STAT1/3 to modulate microglial inflammation, reduces LPS (HY-D1056)-induced pro-inflammatory cytokines (NO, IL-1β, IL-6, and TNF-α) and inflammatory mediators (iNOS, COX-2). STAT1/3-IN-1 exhibits low toxicity in mice. STAT1/3-IN-1 can be used for the research of neuroinflammation.

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Reinheit: 99.23%
CAS. Nr.: 2958649-56-2
Formel: C₂₈H₂₅ClN₆O₅
Molecular Weight:560.99

Speicherung:

Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 6 months , -20°C, 1 month

STAT1/3-IN-1 Chemical Structure

CAS. Nr.: 2958649-56-2

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Biologische Aktivität
- Beschreibung
- IC₅₀ & Target
- In Vitro
- In Vivo
Chemical Information
Publications (2)
Lösungsmittel & Löslichkeit
- In Vitro
- In Vivo
Reinheit & Dokumentation
Verweise
Help & FAQs
Classifications
Bioz

Biologische Aktivität

Beschreibung

IC₅₀ & Target^[1]

COX-2

IL-6

iNOS

STAT3

STAT1

IL-1β

TNF-α

Alle STAT Isoform-spezifische Produkte anzeigen :

Alle NO Synthase Isoform-spezifische Produkte anzeigen :

Alle COX Isoform-spezifische Produkte anzeigen :

Alle Interleukin Related Isoform-spezifische Produkte anzeigen :

Alle TNF Receptor Isoform-spezifische Produkte anzeigen :

In Vitro

STAT1/3-IN-1 (compound 6k) (1-10 μM, 26 h) inhibits LPS-induced NO production with an IC₅₀ of 4.45 μM, while maintains cell viability in BV-2 cells^[1].
STAT1/3-IN-1 (5-10 μM; 8 h) significantly downregulates mRNA expression of pro-inflammatory cytokines (IL-1β, IL-6, TNF-α) and inflammatory mediators (iNOS, COX-2) in LPS-stimulated BV-2 cells^[1].
STAT1/3-IN-1 (5-10 μM) reduces LPS-induced IL-6 and TNF-α release in BV-2 cells^[1].
STAT1/3-IN-1 (5-10 μM; 26 h) dose-dependently reduces iNOS and COX-2 protein expression in LPS-stimulated BV-2 cells^[1].
STAT1/3-IN-1 (5-10 μM; 5 h) inhibits STAT1 and STAT3 phosphorylation and reduces nuclear phosphorylated STAT1 and STAT3 in LPS-stimulated BV-2 cells^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Real Time qPCR^[1]

Cell Line:

LPS-stimulated BV-2 cells
Concentration:

5, 10 μM
Incubation Time:

8 h (2 h pretreatment + 6 h with LPS)
Result:

Significantly downregulated mRNA expression of IL-1β, IL-6, TNF-α, iNOS and COX-2 in LPS-stimulated BV-2 cells.

Western Blot Analysis^[1]

Cell Line:

LPS-stimulated BV-2 cells
Concentration:

5, 10 μM
Incubation Time:

26 h (2 h pretreatment + 24 h with LPS)
Result:

Decreased LPS-induced iNOS and COX-2 protein expression in a concentration-dependent manner.

Western Blot Analysis^[1]

Cell Line:

LPS-stimulated BV-2 cells
Concentration:

5, 10 μM
Incubation Time:

5 h (2 h pretreatment + 3 h with LPS)
Result:

Abrogated LPS-induced phosphorylation of STAT1 and STAT3.

Immunofluorescence^[1]

Cell Line:

LPS-stimulated BV-2 cells
Concentration:

10 μM
Incubation Time:

5 h (2 h pretreatment + 3 h with LPS)
Result:

Significantly reduced nuclear presence of phosphorylated STAT1 and STAT3 under LPS stimulation.

Western Blot Analysis^[1]

Cell Line:

LPS-stimulated BV-2 cells
Concentration:

10 μM
Incubation Time:

5 h (2 h pretreatment + 3 h with LPS)
Result:

Decreased levels of phosphorylated STAT1 and STAT3 in nuclear extracts under LPS stimulation.

Cell Viability Assay^[1]

Cell Line:

LPS-stimulated BV-2 cells
Concentration:

1, 10 μM
Incubation Time:

26 h (2 h pretreatment + 24 h with LPS)
Result:

Showed no significant cytotoxicity, with cell viability of 88.03% (1 μM) and 86.71% (10 μM) compared to the control group.

In Vivo

STAT1/3-IN-1 (compound 6k) (250 mg/kg; i.g.; single dose) shows low acute toxicity in KM mice^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model:

Male and female KM mice^[1]
Dosage:

250 mg/kg
Administration:

i.g.; single dose
Result:

Showed no significant differences in body weight, organ indices, GPT and GOT levels compared to vehicle control.
Showed no significant damage in major organs (heart, liver, spleen, lungs, and kidneys).

Chemical Information

CAS. Nr. 2958649-56-2
Appearance Solid
Molecular Weight 560.99
Formel C₂₈H₂₅ClN₆O₅
Color White to off-white
SMILES

ClC1=C(N2C=C(C3=CC=CC(NC(C4=CN(C[C@@](OCC[C@H]5C)([H])N5C6=O)C6=C(OC)C4=O)=O)=C3)N=N2)C=CC=C1
Versand

Room temperature in continental US; may vary elsewhere.

Speicherung

Powder	-20°C	3 years
	4°C	2 years
In solvent	-80°C	6 months
	-20°C	1 month

Publications (2)

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Journal Impact Factor

Phytother Res

(+)-Matairesinol, Derived From Olive Oil, Enhanced T-Cell Anti-Tumor Immune via JAK3-STAT1 Signal and Synergized With Anti-PD-1 Efficacy. [Abstract]

2026 Apr 27. PMID: 42037203
J Ethnopharmacol

"Shihu" promote T-cell immunity against breast cancer through bioactive constituent THMB enhancing JAK3-STAT1 signal. [Abstract]

2026 Oct 28:369:121888. PMID: 42202911

Lösungsmittel & Löslichkeit

In Vitro:

DMSO : 100 mg/mL (178.26 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

View the Complete Stock Solution Preparation Table

Preparing Stock Solutions

View the Complete Stock Solution Preparation Table

Concentration Solvent Mass

1 mg

5 mg

10 mg

Concentration

Solvent

Mass

1 mM

1.7826 mL

8.9128 mL

17.8256 mL

5 mM

0.3565 mL

1.7826 mL

3.5651 mL

10 mM

0.1783 mL

0.8913 mL

1.7826 mL

Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.

Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Molaritätsrechner

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Konzentration Konzentration

Volumen Volumen

Molecular Weight Molecular Weight

Verdünnungsrechner

Konzentration _{(Stammlösung)} × Volumen _{(Stammlösung)} = Konzentration _{(Ziellösung)} × Volumen _{(Ziellösung)}

Konzentration _{(Stammlösung)} Konzentration _{(Stammlösung)}

Volumen _{(Stammlösung)} Volumen _{(Stammlösung)}

Konzentration _{(Ziellösung)} Konzentration _{(Ziellösung)}

Volumen _{(Ziellösung)} Volumen _{(Ziellösung)}

In Vivo:

Select the appropriate dissolution method based on your experimental animal and administration route.

Stock Solution Working Solution

For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

Protocol 1

Add each solvent one by one: 10% DMSO 90% Corn Oil

Solubility: ≥ 5 mg/mL (8.91 mM); Clear solution

This protocol yields a clear solution of ≥ 5 mg/mL (saturation unknown). If the continuous dosing period exceeds half a month, please choose this protocol carefully.

Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (50.0 mg/mL) to 900 μL Corn oil, and mix evenly.

In Vivo Dissolution Calculator

Please enter the basic information of animal experiments:

Dosage Dosage
mg/kg
Animal Weight (Per Animal) Animal Weight (Per Animal)
g
Dosing Volume (Per Animal) Dosing Volume (Per Animal)
μL
Number of Animals Number of Animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Please enter your animal formula composition:

%
DMSO +

Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
%
+
+
%
Tween-80 + +
%
Saline +

The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).

Working solution concentration: 0.22 mg/mL

Reinheit & Dokumentation

Select Batch:

Reinheit: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (280 KB)
SDS (251 KB)
- English - EN (251 KB)
- Français - FR (251 KB)
- Deutsch - DE (251 KB)
- Norwegian - NO (251 KB)
- Español - ES (251 KB)
- Swedish - SV (251 KB)
- Italian - IT (251 KB)
- Korean - KR (251 KB)
- Portuguese - PT (251 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

Verweise

[1]. Hou X, et al. Synthesis of dolutegravir derivatives modified by 1,2,3-triazole structure and their anti-inflammatory activity in LPS-induced BV2 cells. Bioorg Med Chem Lett. 2025;117:130076. [Content Brief]

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Complete Stock Solution Preparation Table

Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg
DMSO	1 mM	1.7826 mL	8.9128 mL	17.8256 mL	44.5641 mL
	5 mM	0.3565 mL	1.7826 mL	3.5651 mL	8.9128 mL
	10 mM	0.1783 mL	0.8913 mL	1.7826 mL	4.4564 mL
	15 mM	0.1188 mL	0.5942 mL	1.1884 mL	2.9709 mL
	20 mM	0.0891 mL	0.4456 mL	0.8913 mL	2.2282 mL
	25 mM	0.0713 mL	0.3565 mL	0.7130 mL	1.7826 mL
	30 mM	0.0594 mL	0.2971 mL	0.5942 mL	1.4855 mL
	40 mM	0.0446 mL	0.2228 mL	0.4456 mL	1.1141 mL
	50 mM	0.0357 mL	0.1783 mL	0.3565 mL	0.8913 mL
	60 mM	0.0297 mL	0.1485 mL	0.2971 mL	0.7427 mL
	80 mM	0.0223 mL	0.1114 mL	0.2228 mL	0.5571 mL
	100 mM	0.0178 mL	0.0891 mL	0.1783 mL	0.4456 mL

STAT1/3-IN-1

2 Cited Publications

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STAT1/3-IN-1

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Publications Citing Use of MedChemExpress (MCE) STAT1/3-IN-1

Alle STAT Isoform-spezifische Produkte anzeigen

Alle NO Synthase Isoform-spezifische Produkte anzeigen

Alle COX Isoform-spezifische Produkte anzeigen

Alle Interleukin Related Isoform-spezifische Produkte anzeigen

Alle TNF Receptor Isoform-spezifische Produkte anzeigen

Biologische Aktivität

Chemical Information

Publications (2)

Lösungsmittel & Löslichkeit

Reinheit & Dokumentation

Verweise

Help & FAQs

Complete Stock Solution Preparation Table

STAT1/3-IN-1 Related Classifications

HY-170621 Related Classifications