p-Aminophenylmercuric acetate
Based on 11 publication(s) in Google Scholar
p-Aminophenylmercuric acetate is an organomercurial activator of matrix metalloproteinases (MMP). P-Aminophenylmercuric acetate participates in the activation and inhibition of MMP-8 by attacking protein sulfhydryl or inducing cysteine switching reaction. p-Aminophenylmercuric acetate promotes the shedding of betacellulin precursor (pro-BTC). p-Aminophenylmercuric acetate influences the binding of agonists and antagonists to the opiate receptor.
For research use only. We do not sell to patients.
- Purity: 98.32%
- CAS No.: 6283-24-5
- Formula: C8H9HgNO2
- Molecular Weight:351.75
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Storage:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 6 months , -20°C, 1 month
Publications Citing Use of MedChemExpress (MCE) p-Aminophenylmercuric acetate
More- Adv Funct Mater. 2026 Feb 12.
- Adv Sci (Weinh). 2026 Jun 9:e76004. [Abstract]
- Sci Adv. 2025 Jan 17;11(3):eadr8841. [Abstract]
- Biomaterials. 2026 Jun:329:123945. [Abstract]
- Chem Eng J. 2026 Jan 12;529:172936.
- Biomedicines. 2026 Jan 27;14(2):286. [Abstract]
- J Photochem Photobiol B. 2026 May:278:113402. [Abstract]
- Biol Reprod. 2025 Apr 13;112(4):709-727. [Abstract]
- Biochem Biophys Res Commun. 2025 Oct 30:786:152681. [Abstract]
- STAR Protoc. 2025 Jun 20;6(2):103867. [Abstract]
- Hong Kong University. 2025.
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WB
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All Cathepsin Isoforms
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Biological Activity
p-Aminophenylmercuric acetate (APMA) (0-30 µM; 20 min) decreases the apparent number of dihydromorphine binding sites and increases the sensitivity of agonist binding to the inhibitory effects of sodium in rat brain homogenate[2].
p-Aminophenylmercuric acetate (0.5 mM; 30 min) activates the MMP-2 and MMP-9[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 6283-24-5
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Appearance Solid
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Molecular Weight 351.75
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Formula C8H9HgNO2
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Color White to yellow
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SMILES
O=C(C)O[Hg]C1=CC=C(C=C1)N
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month
Publications (11)
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Journal Impact Factor
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Most Recent
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Adv Sci (Weinh)
A Brain-Penetrant Nanobody Reveals GSK3β-Driven Proline-Directed Phosphorylation as a Master Regulator of Ischemic Neurodegeneration. [Abstract]2026 Jun 9:e76004. PMID: 42261803 -
Sci Adv
Peptide-drug conjugates repolarize glioblastoma-associated macrophages to resensitize chemo-immunotherapy of glioblastoma. [Abstract]2025 Jan 17;11(3):eadr8841. PMID: 39823328 -
Biomaterials
Targeting hypersialylation via lectin-directed protein aggregation therapy (LPAT) for anti-metastasis applications. [Abstract]2026 Jun:329:123945. PMID: 41456502 -
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Biomedicines
Environmental Lead Promotes Breast Cancer Migration and Invasion via the AKR1C3-NF-κB-MMP Axis. [Abstract]2026 Jan 27;14(2):286. PMID: 41751184 -
J Photochem Photobiol B
Development of a self-assembling aggregation-induced emission nanoprobe for targeted therapy and real-time imaging in non-small cell lung cancer. [Abstract]2026 May:278:113402. PMID: 41793940 -
Biol Reprod
Collagen turnover during cervical remodeling involves both intracellular and extracellular collagen degradation pathways. [Abstract]2025 Apr 13;112(4):709-727. PMID: 39823285
p-Aminophenylmercuric acetate purchased from MedChemExpress. Usage Cited in: Biol Reprod. 2025 Apr 13;112(4):709-727. [Abstract]
After preincubation with APMA (2 mM, 2 h), a non-enzymatic activator of proMMPs, for 2 h, MMPs significantly degraded collagen monomers compared to non-preincubated APMA samples in both groups.
p-Aminophenylmercuric acetate purchased from MedChemExpress. Usage Cited in: Biol Reprod. 2025 Apr 13;112(4):709-727. [Abstract]
Initial studies showed low endogenous gelatinase activity, but preincubation with APMA (2 mM, 2 h) significantly increased the collagen degradative rate in all the 3 groups.
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Biochem Biophys Res Commun
2025 Oct 30:786:152681. PMID: 41056877 -
STAR Protoc
Protocol for isolating extracellular vesicles from human or mouse airway macrophages for functional assays and in vivo or in vitro experimentation. [Abstract]2025 Jun 20;6(2):103867. PMID: 40460201 -
Solvent & Solubility
DMSO : 100 mg/mL (284.29 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, 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.
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.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
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: ≥ 2.08 mg/mL (5.91 mM); Clear solution
This protocol yields a clear solution of ≥ 2.08 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (20.8 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.
Purity & Documentation
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Data Sheet (272 KB)
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SDS (420 KB)
- English - EN (420 KB)
- Français - FR (420 KB)
- Deutsch - DE (420 KB)
- Norwegian - NO (420 KB)
- Español - ES (420 KB)
- Swedish - SV (420 KB)
- Italian - IT (420 KB)
- Korean - KR (420 KB)
- Portuguese - PT (420 KB)
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Handling Instructions (2659 KB)
References
[1]. Sanderson M P, et al. ADAM10 mediates ectodomain shedding of the betacellulin precursor activated by p-aminophenylmercuric acetate and extracellular calcium influx[J]. Journal of Biological Chemistry, 2005, 280(3): 1826-1837. [Content Brief]
[2]. PASTERNAK G W, et al. Differential effects of protein-modifying reagents on receptor binding of opiate agonists and antagonists[J]. Molecular Pharmacology, 1975, 11(3): 340-351. [Content Brief]
[3]. Gendron R, et al. Inhibition of the activities of matrix metalloproteinases 2, 8, and 9 by chlorhexidine[J]. Clinical Diagnostic Laboratory Immunology, 1999, 6(3): 437-439. [Content Brief]
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, 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 | 2.8429 mL | 14.2146 mL | 28.4293 mL | 71.0732 mL |
| 5 mM | 0.5686 mL | 2.8429 mL | 5.6859 mL | 14.2146 mL | |
| 10 mM | 0.2843 mL | 1.4215 mL | 2.8429 mL | 7.1073 mL | |
| 15 mM | 0.1895 mL | 0.9476 mL | 1.8953 mL | 4.7382 mL | |
| 20 mM | 0.1421 mL | 0.7107 mL | 1.4215 mL | 3.5537 mL | |
| 25 mM | 0.1137 mL | 0.5686 mL | 1.1372 mL | 2.8429 mL | |
| 30 mM | 0.0948 mL | 0.4738 mL | 0.9476 mL | 2.3691 mL | |
| 40 mM | 0.0711 mL | 0.3554 mL | 0.7107 mL | 1.7768 mL | |
| 50 mM | 0.0569 mL | 0.2843 mL | 0.5686 mL | 1.4215 mL | |
| 60 mM | 0.0474 mL | 0.2369 mL | 0.4738 mL | 1.1846 mL | |
| 80 mM | 0.0355 mL | 0.1777 mL | 0.3554 mL | 0.8884 mL | |
| 100 mM | 0.0284 mL | 0.1421 mL | 0.2843 mL | 0.7107 mL |