Paromomycin sulfate salt - BioReagent, for cell culture, ≥98%, powder , CAS No.1263-89-4

CAS: 1263-89-4 Cat. No.: P431665 Peso molecular: 615.63 (free base basis) Número EC: 215-031-7

GRADE & PURITY BioReagent, for Cell culture, ≥98%, powder

Synonyms

SCHEMBL3355 | EN300-245883 | PAROMOMYCIN SULFATE [USP MONOGRAPH] | A883521 | PAROMOMYCIN SULFATE (USP-RS) | Paromomycin sulfate [USP:JAN] | (1,1'-BIPHENYL-2-YL)BORONIC ACID | Humagel | Q27269495 | Aminosidine sulphate | CHEBI:7935 | NSC227228 | D-Streptam

Storage

Room temperature

Descripción general

Chemical structure: aminoglycoside Paromomycin or aminosidine, an aminoglycoside belongs to the class of aminoglycosides. This nonabsorbable antibiotic is found at high level in the lumen of the colon.

Application

Paromomycin sulfate salt has been used as a: reference compound in antileishmanial activity RNA-binding ligand and interacts with aptamer. This interaction prevents the binding (and cutting) of dicer to RNA duplex. Recommended for use in cell culture applications at 100mg/L. Paromomycin sulfate salt has been used as a positive control to compare the purine analog antiviral 2′,3′-dideoxyinosine (ddI).

Other Notes

Keep container tightly closed in a dry and well-ventilated place.Keep in a dry place 1g,5g

Specifications

Sinónimos

SCHEMBL3355 | EN300-245883 | PAROMOMYCIN SULFATE [USP MONOGRAPH] | A883521 | PAROMOMYCIN SULFATE (USP-RS) | Paromomycin sulfate [USP:JAN] | (1, 1'-BIPHENYL-2-YL)BORONIC ACID | Humagel | Q27269495 | Aminosidine sulphate | CHEBI:7935 | NSC227228 | D-Streptam

Especificaciones y pureza

BioReagent, for cell culture, ≥98%, powder

Mecanismos bioquímicos y fisiológicos

Paromomycin possesses antileishmanial and antibacterial activities. It is used to cure visceral leishmaniasis (VL) and cutaneous leishmaniasis (CL). This aminocyclitol glycoside is active against gram-negative and gram-positive bacteria. It is also act

Condiciones de almacenamiento de almacenamiento

Room temperature

Grado

BioReagent, for Cell culture

Tipo de acción

INHIBITOR

Pureza

≥98%

Nombres e identificadores

• Sonrisas canónicas: C1C(C(C(C(C1N)OC2C(C(C(C(O2)CO)O)O)N)OC3C(C(C(O3)CO)OC4C(C(C(C(O4)CN)O)O)N)O)O)N.OS(=O)(=O)O
• IUPAC Name: (2S,3S,4R,5R,6R)-5-amino-2-(aminomethyl)-6-[(2R,3S,4R,5S)-5-[(1R,2R,3S,5R,6S)-3,5-diamino-2-[(2S,3R,4R,5S,6R)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-hydroxycyclohexyl]oxy-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl]oxyoxane-3,4-diol;sulfuric acid
• InChIKey: LJRDOKAZOAKLDU-UDXJMMFXSA-N
• INCHI: 1S/C23H45N5O14.H2O4S/c24-2-7-13(32)15(34)10(27)21(37-7)41-19-9(4-30)39-23(17(19)36)42-20-12(31)5(25)1-6(26)18(20)40-22-11(28)16(35)14(33)8(3-29)38-22;1-5(2,3)4/h5-23,29-36H,1-4,24-28H2;(H2,1,2,3,4)/t5-,6+,7+,8-,9-,10-,11-,12+,13-,14-,15-,16-,17-,18-,19-,20-,21-,22-,23+;/m1./s1
• Isómeros SMILES: C1[C@H]([C@@H]([C@H]([C@@H]([C@H]1N)O[C@@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)N)O[C@H]3[C@@H]([C@@H]([C@H](O3)CO)O[C@@H]4[C@@H]([C@H]([C@@H]([C@@H](O4)CN)O)O)N)O)O)N.OS(=O)(=O)O
• RTECS: WK2320000
• CAS alternativo: 7542-37-2；84420-34-8
• Peso molecular: 615.63 (free base basis)

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Clase Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Level5 Aminosaccharides
          • Level6 Aminoglycosides
            • Level7 Aminocyclitol glycosides
              • Level8 2-deoxystreptamine aminoglycosides
                • Level9 4,5-disubstituted 2-deoxystreptamines

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Aminosaccharides - Aminoglycosides - Aminocyclitol glycosides - 2-deoxystreptamine aminoglycosides
• Direct Parent: 4,5-disubstituted 2-deoxystreptamines
• Alternative Parents: Disaccharides O-glycosyl compounds Aminocyclitols and derivatives Cyclohexanols Cyclohexylamines Organic sulfuric acids Oxanes Tetrahydrofurans 1,2-aminoalcohols Acetals Oxacyclic compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Primary alcohols Organopnictogen compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: 4,5-disubstituted 2-deoxystreptamine - Disaccharide - Glycosyl compound - O-glycosyl compound - Aminocyclitol or derivatives - Cyclohexanol - Cyclohexylamine - Sulfuric acid - Cyclitol or derivatives - Oxane - Cyclic alcohol - Tetrahydrofuran - Organic sulfuric acid or derivatives - Secondary alcohol - 1,2-aminoalcohol - Acetal - Organoheterocyclic compound - Oxacycle - Alcohol - Primary aliphatic amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Amine - Organonitrogen compound - Primary amine - Primary alcohol - Aliphatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as 4,5-disubstituted 2-deoxystreptamines. These are 2-deoxystreptamine aminoglycosides that a glycosidically linked to a pyranose of furanose unit at the C4- and C5-positions.
• 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

Objetivos asociados (humanos)

HEK293 (82097 Activities)

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HFF (3142 Activities)

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PCDH15 Tbio Protocadherin-15 (27 Activities)

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SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)

Discover Target: SLCO1B1

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SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)

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RPSA Tbio 80S Ribosome (239 Activities)

Discover Target: RPSA

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Objetivos asociados (no humanos)

Escherichia coli (133304 Activities)

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Bacillus subtilis (32866 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

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Bacillus spizizenii (1898 Activities)

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Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: H2O: 50mg/mL (store stock solution at 2-8°C. Stable at 37°C for 5 days.)
• Rotación específica [α]: 48° (C=1,H2O)
• Peso molecular: 713.700 g/mol
• Hydrogen Bond Donor Count: 15
• Hydrogen Bond Acceptor Count: 23
• Rotatable Bond Count: 9
• Exact Mass: 713.264 Da
• Monoisotopic Mass: 713.264 Da
• Topological Polar Surface Area: 430.000 Ų
• Heavy Atom Count: 47
• Formal Charge: 0
• Complexity: 952.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 19
• 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

Referencias

1. Lu Qi, Shanshan Liu, Zhen Yan, Min Qiao, Haonan Peng, Liping Ding.  (2023)  A cross-reactive fluorescent ensemble based on perylene derivative/surfactant assemblies for discrimination of multiple aminoglycoside antibiotics in aqueous solution.  JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY,      [PMID:] [10.1016/j.jphotochem.2023.115128]

2. Qiang Chen, Yiyan Cheng, Zhihong Huang, Shuo Du, Quanqian Lyu, Senbin Chen, Juan Tao, Lianbin Zhang, Jintao Zhu.  (2025)  All Drug Glassy Microneedle Patches for Instantaneous Transdermal Delivery.  ADVANCED MATERIALS,      [PMID:40960233] [10.1002/adma.202512849]