Sulfathiazole - ≥98% , Bacterial dihydropteroate synthase inhibitor, CAS No.72-14-0, Bacterial dihydropteroate synthase inhibitor

Name: Sulfathiazole - ≥98% , Bacterial dihydropteroate synthase inhibitor, CAS No.72-14-0, Bacterial dihydropteroate synthase inhibitor
Brand: Aladdin Scientific
SKU: S128351
Availability: InStock

CAS: 72-14-0 Cat. No.: S128351 Summenformel: C₉H₉N₃O₂S₂ Molekulargewicht: 255.32 Beilstein Registry Number: 226178 EG-Nummer: 200-771-5 PubChem CID: 5340

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QUALITÄT & REINHEIT ≥98%

Synonyms

Storage

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Spezifikationen Produkteigenschaften Namen und Kennungen Dokumentation Erweiterte Daten Taxonomic Classification 3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften FAQs und Artikel Citations of This Product Lösungsrechner Bewertungen Häufig gestellte Fragen

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Warum diese Qualität

≥98% für empfindliche chromatographische und analytische Workflows, die minimale Basislinieninterferenzen erfordern.

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Lagerung & Versand

Room temperature Versand Normal. Genaue Spezifikationen finden Sie im chargenspezifischen COA.

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SDS, COA, Datenblatt und Spezifikationsblatt stehen zum Download bereit. Chargenspezifische COA über Chargennummernsuche abrufbar.

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Literaturbeleg

In 66 peer-reviewten Publikationen zu Chromatographie, organischer Synthese und Kreuzkupplungsreaktionen zitiert.

Spezifikationen

Synonyme

Spezifikationen & Reinheit

≥98%

Biochemische und physiologische Mechanismen

Sulfonamide antibiotic that blocks the synthesis of dihydrofolic acid by inhibiting the enzyme dihydropteroate synthase. Mode of Action: Inhibits folic acid synthesis in prokaryotes. Anti-microbial Spectrum: Gram positive, Gram negative, Chlamydia Mode of

Storage

Room temperature

Verschickt in

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Aktionsart

INHIBITOR

Mechanismus der Wirkung

Bacterial dihydropteroate synthase inhibitor

Reinheit

≥98%

Produkteigenschaften

ALogP

0.1

Namen und Kennungen

Pubchem Sid

504750873

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504750873

Kanonisches Lächeln

C1=CC(=CC=C1N)S(=O)(=O)NC2=NC=CS2

IUPAC Name

4-amino-N-(1,3-thiazol-2-yl)benzenesulfonamide

InChIKey

JNMRHUJNCSQMMB-UHFFFAOYSA-N

INCHI

1S/C9H9N3O2S2/c10-7-1-3-8(4-2-7)16(13,14)12-9-11-5-6-15-9/h1-6H,10H2,(H,11,12)

Isomere SMILES

C1=CC(=CC=C1N)S(=O)(=O)NC2=NC=CS2

WGK Deutschland

RTECS

WP2360000

PubChem CID

5340

Molekulargewicht

255.32

Beilstein

226178

Dokumentation

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Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Klasse Benzene and substituted derivatives
    - Subclass Benzenesulfonamides

Kingdom	Organic compounds
Superclass	Benzenoids
Klasse	Benzene and substituted derivatives
Subclass	Benzenesulfonamides
Intermediate Tree Nodes	Not available
Direct Parent	Aminobenzenesulfonamides
Alternative Parents	Benzenesulfonyl compounds Aniline and substituted anilines Organosulfonamides Thiazoles Heteroaromatic compounds Aminosulfonyl compounds Azacyclic compounds Primary amines Organopnictogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic heteromonocyclic compounds
Substituents	Aminobenzenesulfonamide - Benzenesulfonyl group - Aniline or substituted anilines - Organosulfonic acid amide - Azole - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Thiazole - Aminosulfonyl compound - Heteroaromatic compound - Organoheterocyclic compound - Azacycle - Organonitrogen compound - Amine - Organic oxygen compound - Organic nitrogen compound - Organosulfur compound - Organopnictogen compound - Primary amine - Hydrocarbon derivative - Organic oxide - Aromatic heteromonocyclic compound
Beschreibung	This compound belongs to the class of organic compounds known as aminobenzenesulfonamides. These are organic compounds containing a benzenesulfonamide moiety with an amine group attached to the benzene ring.
External Descriptors	a small molecule
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

3D-Struktur

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PDE5A Tclin Phosphodiesterase 5A (5113 Activities)

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EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)

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CA2 Tclin Carbonic anhydrase II (17698 Activities)

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ESR1 Tclin Estrogen receptor alpha (17718 Activities)

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HMGCR Tclin HMG-CoA reductase (2475 Activities)

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NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

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INSR Tclin Insulin receptor (5558 Activities)

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PGR Tclin Progesterone receptor (8562 Activities)

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ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)

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CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)

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ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)

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HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)

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ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)

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AR Tclin Androgen Receptor (11781 Activities)

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CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

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ACE Tclin Angiotensin-converting enzyme (1423 Activities)

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DRD2 Tclin Dopamine D2 receptor (23596 Activities)

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GABRA1 Tclin GABA receptor alpha-1 subunit (399 Activities)

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MAOA Tclin Monoamine oxidase A (11911 Activities)

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CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)

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DRD1 Tclin Dopamine D1 receptor (9720 Activities)

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DRD4 Tchem Dopamine D4 receptor (7907 Activities)

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ACHE Tclin Acetylcholinesterase (18204 Activities)

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PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)

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SLC6A2 Tclin Norepinephrine transporter (10102 Activities)

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HRH2 Tclin Histamine H2 receptor (5428 Activities)

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ADRA1D Tclin Alpha-1d adrenergic receptor (4171 Activities)

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MAOB Tclin Monoamine oxidase B (8835 Activities)

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HTR1B Tclin Serotonin 1b (5-HT1b) receptor (2801 Activities)

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HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)

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HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)

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AVPR2 Tclin Vasopressin V2 receptor (2912 Activities)

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ADORA1 Tclin Adenosine A1 receptor (17603 Activities)

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AGTR1 Tclin Type-1 angiotensin II receptor (5176 Activities)

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CALCR Tclin Calcitonin receptor (2215 Activities)

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SLC6A4 Tclin Serotonin transporter (12625 Activities)

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CRHR1 Tclin Corticotropin releasing factor receptor 1 (2996 Activities)

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ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)

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PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)

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HRH1 Tclin Histamine H1 receptor (7573 Activities)

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ADRA1B Tclin Alpha-1b adrenergic receptor (2912 Activities)

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OPRM1 Tclin Mu opioid receptor (19785 Activities)

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DRD3 Tclin Dopamine D3 receptor (14368 Activities)

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AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)

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OPRD1 Tclin Delta opioid receptor (15096 Activities)

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OPRK1 Tclin Kappa opioid receptor (16155 Activities)

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HTR3A Tclin Serotonin 3a (5-HT3a) receptor (3366 Activities)

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GCGR Tclin Glucagon receptor (2563 Activities)

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SLC6A3 Tclin Dopamine transporter (10535 Activities)

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GRIN1 Tclin Glutamate (NMDA) receptor subunit zeta 1 (122 Activities)

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ddlB D-alanylalanine synthetase (66 Activities)

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murA UDP-N-acetylglucosamine 1-carboxyvinyltransferase (389 Activities)

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Agtr2 Angiotensin II type 2 (AT-2) receptor (803 Activities)

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Mc4r Melanocortin receptor 4 (1205 Activities)

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Ltc4s Leukotriene C4 synthase (1 Activities)

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Sigmar1 Sigma opioid receptor (160 Activities)

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Npy1r Neuropeptide Y receptor type 1 (8 Activities)

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Cckar Cholecystokinin A receptor (90 Activities)

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Ntsr1 Neurotensin receptor 1 (48 Activities)

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Pde4d Phosphodiesterase 4D (4 Activities)

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Bdkrb1 Bradykinin B1 receptor (77 Activities)

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Nos2 Nitric oxide synthase, inducible (3573 Activities)

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Mapk1 MAP kinase ERK2 (650 Activities)

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Hdac6 Histone deacetylase 6 (222 Activities)

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Mmp9 Matrix metalloproteinase 9 (38 Activities)

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folP Dihydropteroate synthase (129 Activities)

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Hcar2 Hydroxycarboxylic acid receptor 2 (55 Activities)

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Streptococcus pneumoniae (31063 Activities)

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Pseudomonas aeruginosa (123386 Activities)

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Klebsiella pneumoniae (43867 Activities)

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Salmonella typhimurium (15756 Activities)

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Pasteurella multocida (1166 Activities)

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Staphylococcus aureus (210822 Activities)

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Staphylococcus epidermidis (22802 Activities)

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Acinetobacter baumannii (41033 Activities)

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Escherichia coli (133304 Activities)

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Enterococcus faecium (13803 Activities)

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Mycobacterium avium (4587 Activities)

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Mycobacterium kansasii (6484 Activities)

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Mycobacterium tuberculosis (203094 Activities)

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Enterococcus faecalis (29875 Activities)

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Lacticaseibacillus casei (578 Activities)

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Plasmodium berghei (192651 Activities)

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Mus musculus (284745 Activities)

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Rattus norvegicus (775804 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

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Proteus sp. (112 Activities)

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lasR Transcriptional activator protein lasR (432 Activities)

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Glra2 Glycine receptor (1745 Activities)

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Wirkungsmechanismen

Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)

C of A & Other Certificates(BSE/TSE, COO):

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18 results found

Lot Number	Certificate Type	Datum	Artikel
J2227790	Certificate of Analysis	Aug 04, 2026	S128351
J2227753	Certificate of Analysis	Aug 04, 2026	S128351
J2227710	Certificate of Analysis	Aug 04, 2026	S128351
J2227697	Certificate of Analysis	Aug 04, 2026	S128351
F2217145	Certificate of Analysis	Apr 02, 2026	S128351
F2217208	Certificate of Analysis	Apr 02, 2026	S128351
A2628168	Certificate of Analysis	Jan 29, 2026	S128351
C2512747	Certificate of Analysis	Jul 29, 2024	S128351
C2512748	Certificate of Analysis	Jul 29, 2024	S128351
C2512749	Certificate of Analysis	Jul 29, 2024	S128351
A2509363	Certificate of Analysis	Jul 06, 2024	S128351
F2615087	Certificate of Analysis	Jul 06, 2024	S128351
A2509369	Certificate of Analysis	Jul 06, 2024	S128351
A2509362	Certificate of Analysis	Jul 06, 2024	S128351
J2411078	Certificate of Analysis	Oct 09, 2022	S128351
J2411079	Certificate of Analysis	Oct 09, 2022	S128351
F2217189	Certificate of Analysis	Jun 01, 2022	S128351
J2331128	Certificate of Analysis	Jun 01, 2022	S128351

Chemische und physikalische Eigenschaften

Löslichkeit	Slightly soluble in water, deuterated dimethyl sulfoxide and ethanol. Soluble in acetone, dilute mineral acids, potassium hydroxide solution, sodium hydroxide solution, ammonia water, dimethyl sulphoxide and methanol.
Schmelzpunkt (°C)	200-202°C
Molekulargewicht	255.300 g/mol
XLogP3	0.100
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	6
Rotatable Bond Count	3
Exact Mass	255.014 Da
Monoisotopic Mass	255.014 Da
Topological Polar Surface Area	122.000 Å²
Heavy Atom Count	16
Formal Charge	0
Complexity	320.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
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	1

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What is the purity of this product?

This product is supplied at ≥98% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.

How should this product be stored?

Store at room temperature.

How is this product shipped?

This product ships under standard ambient conditions. No temperature-controlled packaging is required.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 72-14-0, the molecular formula is C9H9N3O2S2, and the molecular weight is 255.32 g/mol. InChIKey JNMRHUJNCSQMMB-UHFFFAOYSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.

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Other applications36

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Spectroscopy sample preparation5

Drug / compound screening6

Extraction & workup solvent33

Organic synthesis — reaction medium27

Chromatography (HPLC / GC / TLC)12

Crystallization & recrystallization2

Industrial & non-pharma application2

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Sulfathiazole - ≥98% , Bacterial dihydropteroate synthase inhibitor, CAS No.72-14-0, Bacterial dihydropteroate synthase inhibitor

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