Category: pyrazoles-derivatives

Xu, Sheng-jie published the artcileSynthesis and cytotoxicity of some pyrazolic compounds, Name: 4-(1H-Pyrazol-4-yl)pyridine, the publication is Guangzhou Huagong (2012), 40(24), 47-48, database is CAplus.

Seven pyrazole compounds were synthesized and characterized by ¹H NMR and MS, and the cytotoxicity of the compounds on Bel-7402, KB, HL-60, and BGC-823 was tested by MTT assay. The results showed that compound 4f exhibited higher cytotoxicity against Bel-7402 and BGC-823 cell lines.

Guangzhou Huagong published new progress about 19959-71-8. 19959-71-8 belongs to pyrazoles-derivatives, auxiliary class Pyrazole,Pyridine, name is 4-(1H-Pyrazol-4-yl)pyridine, and the molecular formula is C13H10O2, Name: 4-(1H-Pyrazol-4-yl)pyridine.

Referemce:
https://en.wikipedia.org/wiki/Pyrazole,
Pyrazoles – an overview | ScienceDirect Topics

Yu, Lingbo published the artcileSynthesis of 1-alkyl-4-amino-5-pyrazolecarboxylate and ethyl 1-alkyl-5-amino-4-pyrazolecarboxylate, Product Details of C7H11N3O2, the publication is Zhongguo Haiyang Daxue Xuebao, Ziran Kexueban (2006), 36(3), 54-58, database is CAplus.

Synthetic routes to two kinds of substituted pyrazole derivatives were designed based on an anal. of their structural features. The methods for preparing such heterocyclic intermediates, including an N-alkylation reaction condition are researched. The structures of 1-cyclopentyl-4-nitro-5-propyl-1H-pyrazole-3-carboxylic acid Et ester and 1-cyclopentyl-4-nitro-3-propyl-1H-pyrazole-5-carboxylic acid Et ester were identified by HMBC and INEPT NMR techniques.

Zhongguo Haiyang Daxue Xuebao, Ziran Kexueban published new progress about 23286-70-6. 23286-70-6 belongs to pyrazoles-derivatives, auxiliary class Pyrazole,Amine,Ester, name is Ethyl 5-amino-3-methyl-1H-pyrazole-4-carboxylate, and the molecular formula is C15H21BO3, Product Details of C7H11N3O2.

Referemce:
https://en.wikipedia.org/wiki/Pyrazole,
Pyrazoles – an overview | ScienceDirect Topics

Kang, Quan-Peng published the artcileSymmetric containing-PMBP N₂O₂-donors nickel(II) complexes: Syntheses, structures, Hirshfeld analyses and fluorescent properties, Formula: C17H14N2O2, the publication is Polyhedron (2019), 38-50, database is CAplus.

One mononuclear Ni(II) complex [Ni(L¹)(MeOH)₂]·MeOH (1) and two novel trinuclear Ni(II) complexes [Ni₃(L²)₃(EtOH)₆] (2) and [Ni₃(L²)₃(H₂O)₆] (3) constructed from sym. N₂O₂-donors chelating ligands (H₂L¹ and H₂L²) were synthesized and characterized by elemental analyses, FT-IR, UV-Vis spectra and fluorescence spectra. The structures of all three complexes were confirmed by single crystal x-ray diffraction analyses. Complex 1 includes one Ni(II) atom, one completely deprotonated (L¹)^2- unit and two coordinated methanol mols., and forms an infinite 2D supramol. network via the intermol. hydrogen bonds. While complex 2 or 3 is trinuclear with three Ni(II) atoms, three completely deprotonated (L²)^2- units and six coordinated ethanol or H₂O mols. These self-assembling complexes form different dimensional supramol. structures through inter- and intramol. hydrogen bonds. Hirshfeld surface analyses for complexes 1, 2 and 3 were mapped with various functions and further quantification of intermol. interactions was made through the generation of 2D fingerprint plots. In addition, the fluorescence titration experiments were used to characterize fluorescence properties of complexes 1 and 2.

Polyhedron published new progress about 4551-69-3. 4551-69-3 belongs to pyrazoles-derivatives, auxiliary class Benzenes, name is 4-Benzoyl-5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one, and the molecular formula is C17H14N2O2, Formula: C17H14N2O2.

Referemce:
https://en.wikipedia.org/wiki/Pyrazole,
Pyrazoles – an overview | ScienceDirect Topics

Lu, Youcai published the artcileExtraction and Separation of Rare Earths from Nitrate Medium by Mixtures of p-Phosphorylated Calixarene and 1-Phenyl-3-methyl-4-benzoyl-pyrazalone-5, Safety of 4-Benzoyl-5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one, the publication is Chinese Journal of Chemistry (2014), 32(10), 1077-1082, database is CAplus.

The gadolinium extraction by the mixtures of p-phosphorylated calixarene and 1-phenyl-3-methyl-4-benzoyl- pyrazalone-5 from nitrate medium was studied, which indicated an obvious synergistic effect between these two extractants. The extractants exhibit no interaction with each other before the metal extraction Gadolinium(III) was extracted by the species of Ln(PMBP)₂L₂(NO₃) instead of Ln(PMBP)₃·(HPMBP) or Ln(NO₃)₃·2L which are extracted by HPMBP or L alone. Thermodn. functions (ΔG, ΔH, ΔS) were calculated The extraction of other rare earths was also investigated and compared. Possible single rare earth separation was discussed.

Chinese Journal of Chemistry published new progress about 4551-69-3. 4551-69-3 belongs to pyrazoles-derivatives, auxiliary class Benzenes, name is 4-Benzoyl-5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one, and the molecular formula is C17H14N2O2, Safety of 4-Benzoyl-5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one.

Referemce:
https://en.wikipedia.org/wiki/Pyrazole,
Pyrazoles – an overview | ScienceDirect Topics

Guo, Jun-ling published the artcileOne-step synthesis and thermal behavior of 1-methyl-3,4,5-trinitropyrazole, Product Details of C4H6N2, the publication is Hanneng Cailiao (2015), 23(3), 304-306, database is CAplus.

1-Methyl-3, 4 ,5-trinitropyrazole (MTNP) as an insensitive energetic compound was one-step synthesized with 1-methylpyrazole via direct nitration using mixture of nitric acid and fuming sulfuric acid for the first time. The structure of MTNP was characterized by IR, NMR, elemental anal., and mass spectrum. The reaction conditions were optimized as following: reaction temperature 90 °C, reaction time 6 h , molar ratio of HNO₃ and fuming sulfuric acid 1 : 8. At this condition, the yield of MTNP can reach up to 15.2%. Thermal behavior of MTNP was studied by DSC. Results show that its decomposition temperature is 272.0 °C, indicating a good heat stability.

Hanneng Cailiao published new progress about 930-36-9. 930-36-9 belongs to pyrazoles-derivatives, auxiliary class Pyrazole, name is 1-Methylpyrazole, and the molecular formula is C4H6N2, Product Details of C4H6N2.

Referemce:
https://en.wikipedia.org/wiki/Pyrazole,
Pyrazoles – an overview | ScienceDirect Topics

Liu, Mingming published the artcileDiscovery of Novel Aryl Carboxamide Derivatives as Hypoxia-Inducible Factor 1α Signaling Inhibitors with Potent Activities of Anticancer Metastasis, Computed Properties of 763120-58-7, the publication is Journal of Medicinal Chemistry (2019), 62(20), 9299-9314, database is CAplus and MEDLINE.

In order to discover novel hypoxia-inducible factor 1 (HIF-1) inhibitors for the cancer metastasis treatment, 68 new aryl carboxamide compounds were synthesized and evaluated for their inhibitory effect by dual luciferase-reporter assay. Based on five rounds of investigation on structure-activity relationships step by step, compound I was discovered as the most active inhibitor (IC₅₀ = 0.32 μM) with no obvious cytotoxicity (CC₅₀ > 50 μM). It effectively attenuated hypoxia-induced HIF-1α protein accumulation and reduced transcription of vascular epidermal growth factor in a dose-dependent manner, which was further demonstrated by its inhibitory potency on capillary-like tube formation, angiogenesis of zebrafish as well as cellular migration and invasion. Importantly, compound I exhibited antimetastatic potency in breast cancer lung metastasis in the mice model, indicating its promising therapeutic potential for prevention and treatment of tumor metastasis. These results definitely merit attention for further rational design of more efficient HIF-1 inhibitors in the future.

Journal of Medicinal Chemistry published new progress about 763120-58-7. 763120-58-7 belongs to pyrazoles-derivatives, auxiliary class Pyrazole,Boronic acid and ester,Boronic Acids,Boronic acid and ester, name is 1H-Pyrazole-4-boronic acid, and the molecular formula is C3H5BN2O2, Computed Properties of 763120-58-7.

Referemce:
https://en.wikipedia.org/wiki/Pyrazole,
Pyrazoles – an overview | ScienceDirect Topics

Solum, Eirik J. published the artcileSynthesis and biological evaluation of analogs of didehydroepiandrosterone as potential new anticancer agents, Name: 1H-Pyrazole-4-boronic acid, the publication is Molecules (2020), 25(13), 3052, database is CAplus and MEDLINE.

The synthesis, cytotoxicity and inhibition of CDK8 by thirteen analogs I (Ar = C₆H₅, isoquinolin-5-yl, indole-5-yl, etc.) of cortistatin A are reported. These efforts revealed that the analogs with either a 6- or 7-isoquinoline or 5-indole side chain in the 17-position are the most promising anti-proliferative agents. These compounds exhibited potent cytotoxic effects in CEM, HeLa and HMEC-1 cells. All three compounds exhibited IC₅₀ values < 10μM. The analog I (Ar = indole-5-yl) exhibited an IC50 value of 0.59μM towards the human dermal microvascular endothelial cell line (HMEC-1), significantly lower than the reference standard 2-methoxyestradiol. At a concentration at 50 nM the most potent I (Ar = isoquinolin-5-y) compound reduced the activity of CDK8 to 35%.

Molecules published new progress about 763120-58-7. 763120-58-7 belongs to pyrazoles-derivatives, auxiliary class Pyrazole,Boronic acid and ester,Boronic Acids,Boronic acid and ester, name is 1H-Pyrazole-4-boronic acid, and the molecular formula is C7H4ClIO2, Name: 1H-Pyrazole-4-boronic acid.

Referemce:
https://en.wikipedia.org/wiki/Pyrazole,
Pyrazoles – an overview | ScienceDirect Topics

Tng, Jiahui published the artcileAchiral Derivatives of Hydroxamate AR-42 Potently Inhibit Class I HDAC Enzymes and Cancer Cell Proliferation, Name: (1H-Pyrazol-5-yl)boronic acid, the publication is Journal of Medicinal Chemistry (2020), 63(11), 5956-5971, database is CAplus and MEDLINE.

AR-42 is an orally active inhibitor of histone deacetylases (HDACs) in clin. trials for multiple myeloma, leukemia, and lymphoma. It has few hydrogen bond donors and acceptors but is a chiral 2-arylbutyrate and potentially prone to racemization. We report achiral AR-42 analogs incorporating a cycloalkyl group linked via a quaternary carbon atom, with up to 40-fold increased potency against human class I HDACs (e.g., JT86, IC₅₀ 0.7 nM, HDAC1), 25-fold increased cytotoxicity against five human cancer cell lines, and up to 70-fold less toxicity in normal human cells. JT86(I) was ninefold more potent than racAR-42 in promoting accumulation of acetylated histone H4 in MM96L melanoma cells. Mol. modeling and structure-activity relationships support binding to HDAC1 with tetrahydropyran acting as a hydrophobic shield from water at the enzyme surface. Such potent inhibitors of class I HDACs may show benefits in diseases (cancers, parasitic infections, inflammatory conditions) where AR-42 is active.

Journal of Medicinal Chemistry published new progress about 724710-02-5. 724710-02-5 belongs to pyrazoles-derivatives, auxiliary class Pyrazole,Boronic acid and ester,Pyrazole,Boronic Acids,Boronic acid and ester, name is (1H-Pyrazol-5-yl)boronic acid, and the molecular formula is C22H32O2, Name: (1H-Pyrazol-5-yl)boronic acid.

Referemce:
https://en.wikipedia.org/wiki/Pyrazole,
Pyrazoles – an overview | ScienceDirect Topics

Tng, Jiahui published the artcileAchiral Derivatives of Hydroxamate AR-42 Potently Inhibit Class I HDAC Enzymes and Cancer Cell Proliferation, Recommanded Product: 1H-Pyrazole-4-boronic acid, the publication is Journal of Medicinal Chemistry (2020), 63(11), 5956-5971, database is CAplus and MEDLINE.

AR-42 is an orally active inhibitor of histone deacetylases (HDACs) in clin. trials for multiple myeloma, leukemia, and lymphoma. It has few hydrogen bond donors and acceptors but is a chiral 2-arylbutyrate and potentially prone to racemization. We report achiral AR-42 analogs incorporating a cycloalkyl group linked via a quaternary carbon atom, with up to 40-fold increased potency against human class I HDACs (e.g., JT86, IC₅₀ 0.7 nM, HDAC1), 25-fold increased cytotoxicity against five human cancer cell lines, and up to 70-fold less toxicity in normal human cells. JT86(I) was ninefold more potent than racAR-42 in promoting accumulation of acetylated histone H4 in MM96L melanoma cells. Mol. modeling and structure-activity relationships support binding to HDAC1 with tetrahydropyran acting as a hydrophobic shield from water at the enzyme surface. Such potent inhibitors of class I HDACs may show benefits in diseases (cancers, parasitic infections, inflammatory conditions) where AR-42 is active.

Journal of Medicinal Chemistry published new progress about 763120-58-7. 763120-58-7 belongs to pyrazoles-derivatives, auxiliary class Pyrazole,Boronic acid and ester,Boronic Acids,Boronic acid and ester, name is 1H-Pyrazole-4-boronic acid, and the molecular formula is C15H23BO2, Recommanded Product: 1H-Pyrazole-4-boronic acid.

Referemce:
https://en.wikipedia.org/wiki/Pyrazole,
Pyrazoles – an overview | ScienceDirect Topics

Pan, Zhongwei published the artcileStudies on extraction equilibrium of rare earths in ion liquid extraction system using 1-butyl-3-methyl-imidazolium hexafluorophosphate and 1-phenyl-3-methyl-4-benzoyl-pyrazolone-5, Formula: C17H14N2O2, the publication is Advanced Materials Research (Durnten-Zurich, Switzerland) (2013), 602-604(Pt. 2), 887-891, database is CAplus.

The extraction equilibrium of four rare earth ions (REⁿ⁺, n = 3 or 4) was investigated in ionic liquid (IL) extraction system using 1-butyl-3-methyl-imidazolium hexafluorophosphate ([Bmim]PF₆) ionic liquid as extraction solvent and 1-phenyl-3-methyl-4-benzoyl-pyrazolone-5 (HPMBP, HP) as extractant. The extraction percentage could be higher than 99%. The extracted species in the REⁿ⁺-[Bmim]PF₆-HP system was neutral REP_n (n = 3 or 4) and complete recovery of REⁿ⁺ extracted into [Bmim]PF₆ can be achieved using diluent HCl as stripping agent. [Bmim]PF₆ can be recycled in the experiment The extraction equilibrium constants and the pH_1/2 values of four REs and their separation factors between adjacent rare earths were estimated and comparatively studied.

Advanced Materials Research (Durnten-Zurich, Switzerland) published new progress about 4551-69-3. 4551-69-3 belongs to pyrazoles-derivatives, auxiliary class Benzenes, name is 4-Benzoyl-5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one, and the molecular formula is C17H14N2O2, Formula: C17H14N2O2.

Referemce:
https://en.wikipedia.org/wiki/Pyrazole,
Pyrazoles – an overview | ScienceDirect Topics