IMT1B
Based on 10 publication(s) in Google Scholar
IMT1B (LDC203974) is an orally active, noncompetitive and specific allosteric inhibitor of mitochondrial RNA polymerase (POLRMT) and inhibits mitochondrial DNA (mtDNA) expression. IMT1B has anti-tumour effects.
Nur für Forschungszwecke. Wir verkaufen nicht an Patienten.
- Reinheit: 99.45%
- CAS. Nr.: 2304621-06-3
- Formel: C24H21ClFNO6
- Molecular Weight:473.88
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Speicherung:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 2 years , -20°C, 1 year
Publications Citing Use of MedChemExpress (MCE) IMT1B
More- Cell Metab. 2024 Jul 2;36(7):1586-1597.e7. [Abstract]
- Nat Cell Biol. 2023 Nov;25(11):1575-1589. [Abstract]
- Nat Commun. 2026 Jun 15;17(1):5288. [Abstract]
- Exp Mol Med. 2024 Feb;56(2):408-421. [Abstract]
- Cell Death Discov. 2025 Nov 10;11(1):524. [Abstract]
- Int Immunopharmacol. 2025 May 7:157:114778. [Abstract]
- Int Immunopharmacol. 2025 Apr 16:155:114673. [Abstract]
- Mol Biol Cell. 2022 Oct 1;33(12):ar108. [Abstract]
- SSRN. 2025 Dec 15.
- bioRxiv. January 04, 2022.
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RT-PCR
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IF
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RT-PCR
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WB
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RT-PCR
Alle DNA/RNA Synthesis Isoform-spezifische Produkte anzeigen
More
Biologische Aktivität
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RNA Polymerase |
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| A2780 | IC50 |
0.138 μM
Compound: IMT1B
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Antiproliferative activity against human A2780 cells incubated for 168 hrs by SRB method
Antiproliferative activity against human A2780 cells incubated for 168 hrs by SRB method
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[PMID: 36997840] |
| A549 | IC50 |
0.881 μM
Compound: IMT1B
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Antiproliferative activity against human A549 cells incubated for 168 hrs by SRB method
Antiproliferative activity against human A549 cells incubated for 168 hrs by SRB method
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[PMID: 36997840] |
| CAPAN-1 | IC50 |
1.352 μM
Compound: IMT1B
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Antiproliferative activity against human CAPAN-1 cells assessed as cell viability measured after 168 hrs incubation by SRB assay
Antiproliferative activity against human CAPAN-1 cells assessed as cell viability measured after 168 hrs incubation by SRB assay
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[PMID: 39049433] |
| DLD-1 | IC50 |
0.142 μM
Compound: IMT1B
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Antiproliferative activity against human DLD-1 cells incubated for 168 hrs by SRB method
Antiproliferative activity against human DLD-1 cells incubated for 168 hrs by SRB method
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[PMID: 36997840] |
| HeLa | IC50 |
1.052 μM
Compound: IMT1B
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Antiproliferative activity against human HeLa cells incubated for 168 hrs by SRB method
Antiproliferative activity against human HeLa cells incubated for 168 hrs by SRB method
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[PMID: 36997840] |
| HepG2 | IC50 |
0.168 μM
Compound: IMT1B
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Antiproliferative activity against human HepG2 cells incubated for 168 hrs by SRB method
Antiproliferative activity against human HepG2 cells incubated for 168 hrs by SRB method
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[PMID: 36997840] |
| HUVEC | IC50 |
>50 μM
Compound: IMT1B
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Antiproliferative activity against HUVEC cells assessed as cell viability measured after 168 hrs incubation by SRB assay
Antiproliferative activity against HUVEC cells assessed as cell viability measured after 168 hrs incubation by SRB assay
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[PMID: 39049433] |
| IMR-90 | IC50 |
>50 μM
Compound: IMT1B
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Antiproliferative activity against human IMR-90 cells incubated for 168 hrs by SRB method
Antiproliferative activity against human IMR-90 cells incubated for 168 hrs by SRB method
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[PMID: 36997840] |
| MDA-MB-231 | IC50 |
>10 μM
Compound: IMT1B
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Antiproliferative activity against human MDA-MB-231 cells incubated for 168 hrs by SRB method
Antiproliferative activity against human MDA-MB-231 cells incubated for 168 hrs by SRB method
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[PMID: 36997840] |
| MDA-MB-468 | IC50 |
0.189 μM
Compound: IMT1B
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Antiproliferative activity against human MDA-MB-468 cells incubated for 168 hrs by SRB method
Antiproliferative activity against human MDA-MB-468 cells incubated for 168 hrs by SRB method
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[PMID: 36997840] |
| MIA PaCa-2 | IC50 |
0.152 μM
Compound: IMT1B
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Antiproliferative activity against human MIA PaCa-2 cells incubated for 168 hrs by SRB method
Antiproliferative activity against human MIA PaCa-2 cells incubated for 168 hrs by SRB method
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[PMID: 36997840] |
| MIA PaCa-2 | IC50 |
0.159 μM
Compound: IMT1B
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Antiproliferative activity against human MIA PaCa-2 cells assessed as cell viability measured after 168 hrs incubation by SRB assay
Antiproliferative activity against human MIA PaCa-2 cells assessed as cell viability measured after 168 hrs incubation by SRB assay
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[PMID: 39049433] |
| NCI-H1975 | IC50 |
0.221 μM
Compound: IMT1B
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Antiproliferative activity against human NCI-H1975 cells incubated for 168 hrs by SRB method
Antiproliferative activity against human NCI-H1975 cells incubated for 168 hrs by SRB method
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[PMID: 36997840] |
| NCI-H3122 | IC50 |
>10 μM
Compound: IMT1B
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Antiproliferative activity against human NCI-H3122 cells incubated for 168 hrs by SRB method
Antiproliferative activity against human NCI-H3122 cells incubated for 168 hrs by SRB method
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[PMID: 36997840] |
| PANC-1 | IC50 |
1.566 μM
Compound: IMT1B
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Antiproliferative activity against human PANC-1 cells assessed as cell viability measured after 168 hrs incubation by SRB assay
Antiproliferative activity against human PANC-1 cells assessed as cell viability measured after 168 hrs incubation by SRB assay
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[PMID: 39049433] |
| PBMC | IC50 |
>50 μM
Compound: IMT1B
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Antiproliferative activity against human PBMC cells incubated for 168 hrs by SRB method
Antiproliferative activity against human PBMC cells incubated for 168 hrs by SRB method
|
[PMID: 36997840] |
IMT1B is a noncompetitive inhibitor that causes a conformational change of POLRMT, which blocks substrate binding and transcription in a dose-dependent way in vitro[1].
IMT1B (0.01 nM-10 μM; 72-168 hours) dose-dependently decreases in cell viability in A2780, A549 and HeLa cells[1].
IMT1B depletes cellular metabolites[1].
IMT1B increases the levels of mono- and diphosphate nucleotides that results in a considerable increase in the AMP/ATP ratio and levels of phosphorylated AMPK[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:A2780 cells
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Concentration:0.01 nM, 1 nM, 10 nM, 100 nM, 1 μM, 10 μM
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Incubation Time:72 hours, 96 hours, 168 hours
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Result:Decreased cell viability in a dose-dependent manner.
IMT1B reduces mtDNA transcript levels and respiratory-chain subunit levels in tumours[1].
IMT1B exhibits good oral bioavailability (mice 101 %) and Cmax (mice 5149 ng/mL) following oral administration (mice 10 mg/kg)[1].
IMT1B exhibits elimination half-life (mice 1.88 h) due to plasma clearance (mice 0.44 L/h/kg) following intravenous administration (mice 1 mg/kg)[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:7-9 weeks female BALB/c nude mice, with A2780 cells xenograft[1]
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Dosage:100 mg/kg
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Administration:Oral administration, daily, for four weeks
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Result:Led to a clear reduction of tumour volume.
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Animal Model:Mice[1]
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Dosage:1 mg/kg for i.v.; 10 mg/kg for oral (Pharmacokinetic Analysis)
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Administration:Intravenous administration and oral administration
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Result:Oral bioavailability (101%), Cmax (5149 ng/mL), T1/2 (1.88 h).
Chemical Information
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CAS. Nr. 2304621-06-3
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Appearance Solid
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Molecular Weight 473.88
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Formel C24H21ClFNO6
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Color White to off-white
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SMILES
O=C([C@@H]1CN(C([C@H](OC2=CC=C(C(O3)=C2)C(C4=CC=C(F)C=C4Cl)=CC3=O)C)=O)CCC1)O
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Synonyms
LDC203974
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Versand
Room temperature in continental US; may vary elsewhere.
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Speicherung
Powder -20°C 3 years 4°C 2 years In solvent -80°C 2 years -20°C 1 year
Publications (10)
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Journal Impact Factor
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Most Recent
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Cell Metab
A novel protein CYTB-187AA encoded by the mitochondrial gene CYTB modulates mammalian early development. [Abstract]2024 Jul 2;36(7):1586-1597.e7. PMID: 38703762 -
Nat Cell Biol
2023 Nov;25(11):1575-1589. PMID: 37770567
IMT1B purchased from MedChemExpress. Usage Cited in: Nat Cell Biol. 2023 Nov;25(11):1575-1589. [Abstract]
qRT-PCR measurements of MT-CO1 mRNA levels after treatment with IMT1B (500nM) for indicated time in NT or NME6 KO K562 cells.
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Nat Commun
Oncogenic KRAS-driven type I interferon signalling primes pancreatic cancer for necroptosis. [Abstract]2026 Jun 15;17(1):5288. PMID: 42297776 -
Exp Mol Med
Nucleus pulposus cells regulate macrophages in degenerated intervertebral discs via the integrated stress response-mediated CCL2/7-CCR2 signaling pathway. [Abstract]2024 Feb;56(2):408-421. PMID: 38316963
IMT1B purchased from MedChemExpress. Usage Cited in: Exp Mol Med. 2024 Feb;56(2):408-421. [Abstract]
Immunofluorescence staining of dsRNA and mitochondria in rNPCs pretreated with TLR4-IN-C34, MitoTempo or IMT1B (200 nM) for 1 h and then treated with LPS for 6 h.
IMT1B purchased from MedChemExpress. Usage Cited in: Exp Mol Med. 2024 Feb;56(2):408-421. [Abstract]
cl2 and Ccl7 gene expression in rNPCs with or without IMT1B (200 nM) pretreatment for 1 h and LPS treatment for 6 h.
IMT1B purchased from MedChemExpress. Usage Cited in: Exp Mol Med. 2024 Feb;56(2):408-421. [Abstract]
IMT1B (200 nM) pretreatment for 1 h and LPS treatment for 6 h. The expression of PKR-ISR pathway-related proteins in rNPCs.
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Cell Death Discov
Identification of a novel minor-groove DNA binder that represses mitochondrial gene expression and induces apoptosis in highly aggressive leiomyosarcoma cells. [Abstract]2025 Nov 10;11(1):524. PMID: 41213941
IMT1B purchased from MedChemExpress. Usage Cited in: Cell Death Discov. 2025 Nov 10;11(1):524. [Abstract]
Expression levels of the indicated mitochondrial encoded genes in SK-UT-1 cells treated with10 µM of XMH95, Hoechst 33258 or IMT1B. Incubation time was 18 hours for XMH95 and Hoechst 33258, and 48 hours for IMT1B. RNAs were extracted at the indicated processed for qRT-PCR.
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Int Immunopharmacol
STING-mediated mitochondrial DNA release exacerbates PANoptosis in liver ischemia reperfusion injury. [Abstract]2025 May 7:157:114778. PMID: 40339491 -
Int Immunopharmacol
mtDNA/RNA boosts radiation-induced abscopal effect via M1 macrophage polarization-promoted IFN-β-dependent inflammatory response. [Abstract]2025 Apr 16:155:114673. PMID: 40245773 -
Mol Biol Cell
2022 Oct 1;33(12):ar108. PMID: 35921164 -
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Lösungsmittel & Löslichkeit
DMSO : 200 mg/mL (422.05 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)
Select the appropriate dissolution method based on your experimental animal and administration route.
- 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.
Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline
Solubility: ≥ 5 mg/mL (10.55 mM); Clear solution
This protocol yields a clear solution of ≥ 5 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (50.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.
Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
Please enter the basic information of animal experiments:
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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
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%DMSO +
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
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%+
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+%Tween-80 + +
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%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
Method for preparing stock solution: mg drug dissolved in μL DMSO. Stock solution concentration: mg/mL.
1. Take μL DMSO stock solution;
2. Add μL .
μL , mix evenly;
3. Then add μL Tween 80, mix evenly;
4. Then add μL
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
Reinheit & Dokumentation
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Data Sheet (277 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Portuguese - PT (393 KB)
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Handling Instructions (2659 KB)
Verweise
Complete Stock Solution Preparation Table
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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 2.1102 mL | 10.5512 mL | 21.1024 mL | 52.7560 mL |
| 5 mM | 0.4220 mL | 2.1102 mL | 4.2205 mL | 10.5512 mL | |
| 10 mM | 0.2110 mL | 1.0551 mL | 2.1102 mL | 5.2756 mL | |
| 15 mM | 0.1407 mL | 0.7034 mL | 1.4068 mL | 3.5171 mL | |
| 20 mM | 0.1055 mL | 0.5276 mL | 1.0551 mL | 2.6378 mL | |
| 25 mM | 0.0844 mL | 0.4220 mL | 0.8441 mL | 2.1102 mL | |
| 30 mM | 0.0703 mL | 0.3517 mL | 0.7034 mL | 1.7585 mL | |
| 40 mM | 0.0528 mL | 0.2638 mL | 0.5276 mL | 1.3189 mL | |
| 50 mM | 0.0422 mL | 0.2110 mL | 0.4220 mL | 1.0551 mL | |
| 60 mM | 0.0352 mL | 0.1759 mL | 0.3517 mL | 0.8793 mL | |
| 80 mM | 0.0264 mL | 0.1319 mL | 0.2638 mL | 0.6594 mL | |
| 100 mM | 0.0211 mL | 0.1055 mL | 0.2110 mL | 0.5276 mL |