Tetrapyrroles and derivatives
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Filtered Search Results
Medchemexpress LLC Zinc phthalocyanine (ZnPc) | 14320-04-8 | 98.0% | 577.90 | 500 MG
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Zinc phthalocyanine (ZnPc) is a compound utilized in various industrial and biomedical applications. It functions as a catalyst and photoconductor, and shows potential in photodynamic therapy (PDT) and solar-cell applications. It is also capable of photooxidizing cyclohexane.
- Inhibits cancer cell growth in Kyse-140 and OE-33 lines.
- Functions as a photosensitizer, producing reactive oxygen species (ROS) under 694 nm light irradiation.
- Impairs mitochondrial membrane integrity, activates caspase-3, and induces apoptosis in cancer cells.
- Causes long-term damage to the microvascular network in chick chorioallantoic membrane (CAM) models.
- Exhibits antitumor activity in chick chorioallantoic membrane models.
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FUJIFILM BIOSCIENCES INC Lucifer Yellow CH Dilithium Sa
Lucifer Yellow CH Dilithium Salt 6-Amino-2- hydrazinocarbonylamino -23-dihydro-13-dioxo-1H-benz de isoquinoline-58-disulfonic acid dilithium salt is fluorescence dye Ex/Em 428/536 of neurons with higher solubility compared with the Lucifer Yellow CH 2K It can be used for studies on morphology of intracellular neurons For research use only RUO
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Abcam A 769662, AMP-activated protein kinase activator, 50MG
MW 360.4 Da, Purity >99%. Potent, reversible activator of AMP-activated protein kinase (AMPK) (EC₅₀ = 0.8 μM). Directly activates native rat AMPK by mimicking the effects of AMP - it activates AMPK both allosterically and by inhibiting dephosphorylation of AMPK. Shown to inhibit Na+-K+-ATPase at higher concentrations (IC₅₀ = 57 μM) . Inhibits differentiation of adipocytes.
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Abcam GM 6001, MMP inhibitor, 5MG
MW 388.5 Da, Purity >98%. Broad spectrum potent MMP inhibitor. Ki values are 0.4 (MMP-1), 0.5 (MMP-2), 27 (MMP-3), 0.1 (MMP-8), 0.2 (MMP-9), 13.4 (MMP-14) and 0.36 (MMP-26) nM. IC₅₀ value for MMP-7 is 3.7 nM. Pharmacologically active in vivo.
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Abcam SB 216763, GSK3 inhibitor, 1MG
MW 371.2 Da, Purity >98%. Potent and selective GSK3 inhibitor (Ki= 9 nM for GSK-3α). Has little activity against 24 other protein kinases (IC₅₀ > 10 μM). Stimulates glycogen synthesis, gene transcription and is cardio- and neuroprotective.
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Abcam GS 39783, GABAB positive allosteric modulator, 50MG
MW 337.4 Da, Purity >99%. Novel, GABAB positive allosteric modulator (EC50 = 3 μM for [35S]GTPγS binding). Shows anxiolytic and antiaddictive effects *in vivo.* Blood-brain barrier permeable*.* Orally active.
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Abcam Lactacystin, proteasome inhibitor, 200UG
MW 376.4 Da, Purity >95%. Potent, irreversible, cell-permeable, selective 20S proteasome inhibitor (IC₅₀ = 70 nM). Inhibits cell-cycle progression and induces neurite outgrowth in vitro. Anti-bacterial and antitumor agent. Active in vivo and in vitro.
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Apexbio Technology LLC BILIRUBIN 20MG
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BILIRUBIN 20MG APEXBIO TECHNOLOGIES
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Sigma Aldrich Fine Chemicals Biosciences Biliverdin hydrochloride 950MG
Biliverdinnbsp(BV) is considered as a near-infrared (NIR)-absorbing pigment that is endogenic.
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eMolecules Zinc phthalocyanine | 14320-04-8 | MFCD00041955 | 25g
Combi-Blocks | Zinc phthalocyanine | 25g | 296392447 | QC-0016 | 95.000 | 14320-04-8 | MFCD00041955 | 577.920 | C32H16N8Zn
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Abcam omega-Agato x in IVA, Ca2+ channel blocker (P and Q type), 100UG
MW 5202 Da. omega-Agatoxin IVA, Ca2+ channel blocker (P and Q type). Achieve your results faster with highly validated, pure and trusted compounds.
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Abcam [Pyr1]-Apelin 13, endogenous apelin receptor (APJ) agonist, 1MG
MW 1533.8 Da, Purity >95%. [Pyr1]-Apelin 13, endogenous apelin receptor (APJ) agonist. Achieve your results faster with highly validated, pure and trusted compounds.
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Abcam E x endin-4 (E x enatide), GLP-1 receptor agonist, 500UG
MW 4187 Da, Purity >95%. Exendin-4 (Exenatide), GLP-1 receptor agonist. Achieve your results faster with highly validated, pure and trusted compounds.
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Abcam MPEP hydrochloride, mGlu5 antagonist, 10MG
MW 229.7 Da, Purity >99%. Subtype selective and potent non-competitive mGlu₅ antagonist (IC₅₀ = 36 nM). Central effects following systemic administration in vivo.
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Abcam L-threo-PDMP, 10MG
MW 427.03 g/mol, Purity >98%. Enantiomer of D-threo-PDMP (Asc 4052). Activates glycosyltransferases for ganglioside biosynthesis. Antineurodegenerative properties. Active in vivo and in vitro.
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