Phenanthrenes and derivatives
TARGETMOL CHEMICALS INC Aristolochic acid A 100MG
Also available in 1 mL, 10 mg, 25 mg, 50 mg, 500 mg and bulk. Please contact Fisher for quotes. Aristolochic acid A (TR 1736) is a compound of mutagenic, carcinogenic, and nephrotoxic compounds commonly found in the Birthwort (Aristolochiaceae) family of plants. Purity 99.97%
Medchemexpress LLC Aristolochic acid D (Aristolochic acid-IVa) | 17413-38-6 | 357.27 | 1 MG
Aristolochic acid D (Aristolochic acid-IVa) is an orally active PDE2 and CDK2 inhibitor isolated from *Aristolochia indica L.* It exhibits anti-inflammatory activity and can be used in the research of inflammation and tumor-related diseases.
- Orally active PDE2 inhibitor
- Orally active CDK2 inhibitor
- Isolated from *Aristolochia indica L.*
- Exhibits anti-inflammatory activity
- Non-carcinogenic
- Non-nephrotoxic
- Can be used in inflammation research
- Can be used in tumor-related diseases research
Cayman Chemical ArIstolochIc AcId 25mg
A PLA2 inhibitor (IC50 = 40 µM in human neutrophils); inhibits human synovial fluid PLA2-induced edema in a dose-dependent manner in vivo; inhibits hemolytic activity of the PLA2 enzymes TFV PL-X, TFV PL-Ia, and TFV PL-Ib from T. flavoviridis venom (IC50s = 4.6, 4.0, and 3.9 µM, respectively); enhances the edema-inducing activity of TFV PL-Ia and TFV PL-Ib; associated with progressive interstitial fibrosing nephropathy and upper urinary tract urothelial carcinomas
Cayman Chemical ArIstolochIc AcId 50mg
A PLA2 inhibitor (IC50 = 40 µM in human neutrophils); inhibits human synovial fluid PLA2-induced edema in a dose-dependent manner in vivo; inhibits hemolytic activity of the PLA2 enzymes TFV PL-X, TFV PL-Ia, and TFV PL-Ib from T. flavoviridis venom (IC50s = 4.6, 4.0, and 3.9 µM, respectively); enhances the edema-inducing activity of TFV PL-Ia and TFV PL-Ib; associated with progressive interstitial fibrosing nephropathy and upper urinary tract urothelial carcinomas
eMolecules Medchem Express / Aristolochic acid B / 1mg / 527573755 / HY-N0511 / / 475-80-9 / MFCD01708574 / 311.249 / C16H9NO6
Medchem Express / Aristolochic acid B / 1mg / 527573755 / HY-N0511 / / 475-80-9 / MFCD01708574 / 311.249 / C16H9NO6
Sigma Aldrich Fine Chemicals Biosciences Aristolochic acid I European Pharmacopoeia (EP) Reference Standard | 313-67-7 | MFCD00004996 |
Aristolochic acid I European Pharmacopoeia (EP) Reference Standard | Mol Wt: 341.27 | 313-67-7 | MFCD00004996 |
Medchemexpress LLC Aristolochic acid C | 4849-90-5 | 327.25 | 5 MG
Aristolochic acid C is a derivative of Aristolochic acid. Aristolochic acid acts as a phospholipase A2 (PLA2) inhibitor, which interferes with cortical microtubule arrays and root growth in Arabidopsis.
- Derivative of Aristolochic acid
- Acts as a phospholipase A2 (PLA2) inhibitor
- Disrupts cortical microtubule arrays
- Interferes with root growth in Arabidopsis
Medchemexpress LLC Aristolochic acid A | 313-67-7 | MFCD00004996 | 99.9% | 10 MG
Aristolochic acid A is a nitrophenanthrene carboxylic acid supplied as a high-purity research reagent for biochemical and cell-based studies. It is commonly used to investigate NF-κB and AP-1 signaling pathways and for mechanistic studies of nephrotoxicity and carcinogenesis.
- High purity (99.9%).
- Molecular formula C17H11NO7; molecular weight 341.27 g/mol.
- Typically supplied as a 10 mg quantity suitable for research use.
- Used in studies of NF-κB and AP-1 inhibition and mechanisms of nephrotoxicity and carcinogenicity.
- Handle as a toxic and carcinogenic compound with appropriate safety precautions.
Medchemexpress LLC Aristolochic acid Va | 108779-46-0 | 357.27 | 1 MG
Aristolochic acid Va is a natural compound isolated from *Aristolochia* plants. This high-purity compound is intended for research use only, supporting a wide range of studies in natural product chemistry and biological activity.
- Natural compound isolated from Aristolochia plants.
- Suitable for various research applications.
- High purity for reliable experimental results.
- Available in multiple sizes for research flexibility.
Medchemexpress LLC Aristolochic acid D (Aristolochic acid-IVa) | 17413-38-6 | 357.27 | 1 ML
Aristolochic acid D (Aristolochic acid-IVa) is an orally active inhibitor of PDE2 (IC50: 4.673 μM) and CDK2 (IC50: 25 μM) that is isolated from Aristolochia indica L. It demonstrates anti-inflammatory activity and is considered non-carcinogenic and non-nephrotoxic. This compound is suitable for research related to inflammation and tumor-related diseases.
- Orally active PDE2 inhibitor (IC50: 4.673 μM).
- CDK2 inhibitor (IC50: 25 μM).
- Isolated from Aristolochia indica L.
- Exhibits anti-inflammatory activity.
- Non-carcinogenic.
- Non-nephrotoxic.
- Useful in research for inflammation and tumor-related diseases.
TARGETMOL CHEMICALS INC Aristolochic acid B 5MG
Also available in 1 mL, 1 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Aristolochic acid B (Aristolochic Acid II) is a natural product from the Aristolochaceae taxon and is one of the main components of aristolochic acid. Aristolochic acid is a mutagen and carcinogen, and Aristolochic acid B (Aristolochic Acid II) can show a greater carcinogenic risk in vivo than Aristolochic acid I. Purity 99.99%
Chem-Impex International, Inc. 9,10-Phenanthrenequinone | MFCD00001163 | 100G
9,10-Phenanthrenequinone, MFCD00001163, 100G
Electron Microscopy Sciences Rosin Alcohol Working Solution 500 ML
Used in Wolbach's Giemsa Method Wolbach, Todd, and Palfrey (1922) Nuclei, collagen. References are Wolbach, S.B., Todd, J.L. and Palfrey, F.W., The Etilogy of Pathology Typhus, Harvard University Press, Cambridge, MA., p. 13 – 14,c 1922 and Luna, L.G., (ed), Manual of Histologic Staining Methods of the AFIP, 3rd Edition, McGraw-Hill, Y, p. 119, c. 1968
Electron Microscopy Sciences Rosin Alcoholic Stock Solution 250 ML
Used in Wolbach's Giemsa Method, Wolbach, Todd, and Palfrey (1922) for the staining of : nuclei, collagen, riskettsia and bacteria. See references Wolbach, S.B., Todd, J.L., and Paltrey, F.W., The Etiology of Pathology Typhus, Harvard University Press, Cambridge, MA, p. 13-14, c. 1922 and Luna, L.G., (ed). Manual of Histologic Staining Methods od the AFIP, 3rd edition. McGraw-Hill, NY, p. 119, c. 1968.
Medchemexpress LLC Hypericin | 548-04-9 | 504.443 | 1 MG
Hypericin is a naturally occurring substance found in Hypericum perforatum L. It functions as an inhibitor of PKC (protein kinase C), MAO (monoaminoxidase), dopamine-beta-hydroxylase, reverse transcriptase, telomerase, and CYP (cytochrome P450). It exhibits antitumor, antiviral, and antidepressive activities, and can induce apoptosis.
- Inhibits PKC (protein kinase C)
- Inhibits MAO (monoaminoxidase)
- Inhibits dopamine-beta-hydroxylase
- Inhibits reverse transcriptase
- Inhibits telomerase
- Inhibits CYP (cytochrome P450)
- Shows antitumor activity
- Shows antiviral activity
- Shows antidepressive activity
- Induces apoptosis
- Relevant for infection research
- Relevant for neurological disease research
- Relevant for cancer research