Sutezolid - ≥99% , 70S ribosome inhibitor, CAS No.168828-58-8, 70S ribosome inhibitor

CAS: 168828-58-8 Cat. No.: S650066 Peso molecular: 353.41 Número EC: 809-216-7 PubChem CID: 465951
Disponible para pedir
GRADE & PURITY ≥99%
Synonyms
NH-125; NH 125;eEF-2 Kinase Inhibitor, NH125 | SUTEZOLID [WHO-DD] | Sutezolid (USAN/INN) | U-480 | Oxazolidininone | DTXSID20168611 | HY-10251 | AS-74370 | 9EN | cis-3-(Benzyloxymethyl)cyclobutanol, 97% | HY-10392 | N-{[(5S)-3-[3-FLUORO-4-(THIOMORPHOLIN-4
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5mg
S650066-5mg
3

21,90US$

32,90US$
Guardar 11,00 US$ (33.43%)
10mg
S650066-10mg
3

32,90US$

49,90US$
Guardar 17,00 US$ (34.07%)
25mg
S650066-25mg
2

47,90US$

71,90US$
Guardar 24,00 US$ (33.38%)
50mg
S650066-50mg
1

71,90US$

107,90US$
Guardar 36,00 US$ (33.36%)
100mg
S650066-100mg
1

107,90US$

161,90US$
Guardar 54,00 US$ (33.35%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

In Vivo

Sutezolid (PNU-100480) is a thiomorpholinyl analog of linezolid with superior efficacy against M. tuberculosis in the hollow-fiber, mouse, and whole-blood models. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Form:Solid

IC50& Target:Oxazolidinone

Specifications

Sinónimos
NH-125; NH 125;eEF-2 Kinase Inhibitor, NH125 | SUTEZOLID [WHO-DD] | Sutezolid (USAN/INN) | U-480 | Oxazolidininone | DTXSID20168611 | HY-10251 | AS-74370 | 9EN | cis-3-(Benzyloxymethyl)cyclobutanol, 97% | HY-10392 | N-{[(5S)-3-[3-FLUORO-4-(THIOMORPHOLIN-4
Especificaciones y pureza
≥99%
Mecanismos bioquímicos y fisiológicos
Sutezolid (PNU-100480), an active oxazolidinone antimicrobial agent, acts by inhibiting bacterial protein synthesis . Sutezolid has potent activity against mycobacteria , and is used for the research of drug-resistant tuberculosis.
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Tipo de acción
INHIBITOR
Mecanismo de acción
70S ribosome inhibitor
Pureza
≥99%
Propiedades del producto
ALogP1.5
Nombres e identificadores
Sonrisas canónicasCC(=O)NCC1CN(C(=O)O1)C2=CC(=C(C=C2)N3CCSCC3)F
IUPAC NameN-[[(5S)-3-(3-fluoro-4-thiomorpholin-4-ylphenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide
InChIKeyFNDDDNOJWPQCBZ-ZDUSSCGKSA-N
INCHI1S/C16H20FN3O3S/c1-11(21)18-9-13-10-20(16(22)23-13)12-2-3-15(14(17)8-12)19-4-6-24-7-5-19/h2-3,8,13H,4-7,9-10H2,1H3,(H,18,21)/t13-/m0/s1
Isómeros SMILES CC(=O)NC[C@H]1CN(C(=O)O1)C2=CC(=C(C=C2)N3CCSCC3)F
PubChem CID 465951
Peso molecular 353.41

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseThiazinanes
SubclassThiomorpholines
Intermediate Tree Nodes Not available
Direct ParentPhenylthiomorpholines
Alternative Parents Aniline and substituted anilines  Dialkylarylamines  Fluorobenzenes  Oxazolidinones  Aryl fluorides  Acetamides  Carbamate esters  Secondary carboxylic acid amides  Organic carbonic acids and derivatives  Dialkylthioethers  Azacyclic compounds  Oxacyclic compounds  Hydrocarbon derivatives  Organofluorides  Organopnictogen compounds  Carbonyl compounds  Organic oxides  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents 4-phenylthiomorpholine - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Aniline or substituted anilines - Fluorobenzene - Halobenzene - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Oxazolidinone - Acetamide - Carbamic acid ester - Oxazolidine - Carboxamide group - Amino acid or derivatives - Tertiary amine - Carbonic acid derivative - Secondary carboxylic acid amide - Oxacycle - Azacycle - Dialkylthioether - Carboxylic acid derivative - Thioether - Organic oxygen compound - Organic oxide - Amine - Hydrocarbon derivative - Carbonyl group - Organopnictogen compound - Organohalogen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Aromatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as phenylthiomorpholines. These are compounds containing a thiomorpholine ring conjugated to a phenyl group. Thiomorpholine a six-membered aliphatic ring containing one nitrogen atom and one sulfur atom at positions 1 and 4 respectively, and four carbon atoms.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
MAOB Tclin Amine oxidase [flavin-containing] B (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOB Tclin Monoamine oxidase B (8835 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MT4 (17854 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HEK293 (82097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HepG2 (196354 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FECH Tchem Ferrochelatase, mitochondrial (678 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HMBS Tbio Porphobilinogen deaminase (404 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Acinetobacter baumannii (41033 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycobacterium (258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycobacterium avium (4587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycolicibacterium fortuitum (1335 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycobacterium tuberculosis (203094 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycobacterium simiae (3 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycolicibacterium smegmatis (8003 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycobacterium malmoense (3 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycobacterium xenopi (84 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Vero (26788 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

10 results found

Lot NumberCertificate TypeFechaArticulo
I2411275Certificate of AnalysisJul 26, 2024 S650066
I2411276Certificate of AnalysisJul 26, 2024 S650066
I2411277Certificate of AnalysisJul 26, 2024 S650066
I2411278Certificate of AnalysisJul 26, 2024 S650066
I2411279Certificate of AnalysisJul 26, 2024 S650066
I2411280Certificate of AnalysisJul 26, 2024 S650066
I2411281Certificate of AnalysisJul 26, 2024 S650066
I2411282Certificate of AnalysisJul 26, 2024 S650066
I2411283Certificate of AnalysisJul 26, 2024 S650066
I2411284Certificate of AnalysisJul 26, 2024 S650066
Propiedades químicas y físicas
SolubilidadDMSO : 50 mg/mL (141.48 mM; Need ultrasonic)
Peso molecular353.400 g/mol
XLogP31.500
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count6
Rotatable Bond Count4
Exact Mass353.121 Da
Monoisotopic Mass353.121 Da
Topological Polar Surface Area87.200 Ų
Heavy Atom Count24
Formal Charge0
Complexity475.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculadoras de soluciones
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