S-Gboxin - ≥96% , CAS No.2101317-21-7

CAS: 2101317-21-7 Cat. No.: S412174 Formule: C₂₇H₃₂F₃IN₂O₂ Poids moléculaire: 600.45 PubChem CID: 137628665

GRADE & PURITY ≥96%

Synonyms

AKOS037649109 | A936428 | 2101317-21-7 (iodide) | BS-16592 | 2101317-21-7 | EX-A2979 | [(1R,2S,5R)-5-methyl-2-propan-2-ylcyclohexyl] 2-[3-methyl-2-[3-(trifluoromethyl)phenyl]benzimidazol-3-ium-1-yl]acetate;iodide | 3-(2-(((1R,2S,5R)-2-isopropyl-5-methylcy

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Vue d’ensemble

Information

S-Gboxin S-Gboxin, a functional analogue of Gboxin, is an oxidative phosphorylation (OXPHOS) inhibitor which inhibits growth of mouse and human glioblastoma (GBM) with IC50 of 470 nM.

Targets

OXPHOS ; GBM (Cell-based assay) ; 470 nM

Specifications

Synonymes

AKOS037649109 | A936428 | 2101317-21-7 (iodide) | BS-16592 | 2101317-21-7 | EX-A2979 | [(1R,2S,5R)-5-methyl-2-propan-2-ylcyclohexyl] 2-[3-methyl-2-[3-(trifluoromethyl)phenyl]benzimidazol-3-ium-1-yl]acetate;iodide | 3-(2-(((1R,2S,5R)-2-isopropyl-5-methylcy

Spécifications et pureté

≥96%

Mécanismes biochimiques et physiologiques

S-Gboxin, a functional analogue of Gboxin, is an oxidative phosphorylation (OXPHOS) inhibitor which inhibits growth of mouse and human glioblastoma (GBM) with IC50 of 470 nM.

Conditions de stockage de stockage

Store at -20°C

Expédié en

Ice chest + Ice pads

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Pureté

≥96%

Propriétés du produit

• ALogP: 4.587
• Liaison rotative: 7

Noms et identifiants

• Pubchem Sid: 504773503
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504773503
• Sourires canoniques: CC1CCC(C(C1)OC(=O)CN2C3=CC=CC=C3[N+](=C2C4=CC(=CC=C4)C(F)(F)F)C)C(C)C.[I-]
• IUPAC Name: [(1R,2S,5R)-5-methyl-2-propan-2-ylcyclohexyl] 2-[3-methyl-2-[3-(trifluoromethyl)phenyl]benzimidazol-3-ium-1-yl]acetate;iodide
• InChIKey: DCAJNAWCJSUZDG-DZJKTSMVSA-M
• INCHI: 1S/C27H32F3N2O2.HI/c1-17(2)21-13-12-18(3)14-24(21)34-25(33)16-32-23-11-6-5-10-22(23)31(4)26(32)19-8-7-9-20(15-19)27(28,29)30;/h5-11,15,17-18,21,24H,12-14,16H2,1-4H3;1H/q+1;/p-1/t18-,21+,24-;/m1./s1
• Isomères SMILES: C[C@@H]1CC[C@H]([C@@H](C1)OC(=O)CN2C3=CC=CC=C3[N+](=C2C4=CC(=CC=C4)C(F)(F)F)C)C(C)C.[I-]
• PubChem CID: 137628665
• Poids moléculaire: 600.45

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Level5 Amino acids and derivatives
          • Level6 Alpha amino acids and derivatives
            • Level7 Alpha amino acid esters

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Amino acids and derivatives - Alpha amino acids and derivatives
• Direct Parent: Alpha amino acid esters
• Alternative Parents: Phenylimidazoles Trifluoromethylbenzenes Menthane monoterpenoids Bicyclic monoterpenoids Aromatic monoterpenoids Benzimidazoles N-substituted imidazoles Heteroaromatic compounds Carboxylic acid esters Propargyl-type 1,3-dipolar organic compounds Monocarboxylic acids and derivatives Carboximidamides Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organofluorides Organic oxides Organic iodide salts Hydrocarbon derivatives Alkyl fluorides
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Alpha-amino acid ester - 2-phenylimidazole - Trifluoromethylbenzene - P-menthane monoterpenoid - Monoterpenoid - Bicyclic monoterpenoid - Aromatic monoterpenoid - Benzimidazole - Benzenoid - N-substituted imidazole - Monocyclic benzene moiety - Heteroaromatic compound - Imidazole - Azole - Carboxylic acid ester - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic iodide salt - Organic salt - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Alkyl halide - Alkyl fluoride - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as alpha amino acid esters. These are ester derivatives of alpha amino acids.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: Solubility (25°C) In vitro DMSO: 100 mg/mL (166.54 mM); Ethanol: 100 mg/mL (166.54 mM); Water: ˂1 mg/mL
• DMSO (mg/mL) Solubilité maximale: 100
• DMSO (mM) Solubilité maximale: 166.541760346407
• Eau (mg/mL) Solubilité maximale: ˂1
• Poids moléculaire: 600.500 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 6
• Exact Mass: 600.146 Da
• Monoisotopic Mass: 600.146 Da
• Topological Polar Surface Area: 35.100 Ų
• Heavy Atom Count: 35
• Formal Charge: 0
• Complexity: 700.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 3
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

XLogP3

Références

1. Zhuojia Xie, Zhengguang Zou, Changji Xu, Shenglin Zhong, Min Feng, Xinyu Jiang, Weijian Zhang, Xiuxin Zheng, Wenbin He.  (2024)  Changes in microstructure, magnetocaloric effect and critical behavior of La0.8Sr0.2MnO3 manganites by K/Co doping.  CHINESE JOURNAL OF PHYSICS,      [PMID:] [10.1016/j.cjph.2024.05.038]