(R)-Sulforaphane - Moligand™, ≥98% , CAS No.142825-10-3

CAS: 142825-10-3 Cat. No.: R131741 Summenformel: C6H11NOS2 Molekulargewicht: 177.29
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QUALITÄT & REINHEIT Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98%
Synonyms
HY-13755A | 1-isothiocyanato-4-[(R)-methanesulfinyl]butane | 1-Propanamine, 2-chloro-N,N-dimethyl-, hydrochloride (1:1) | (R)-1-Isothiocyanato-4-(methylsulfinyl)butane | GA49J4310U | 2-Piperidinemethanol, 97% | SULFORAPHANE [MI] | SULFORAPHANE [INCI] | (R
Storage
Protected from light,Store at -20°C
Shipped In
Ice chest + Ice pads
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Größe
Deutschland (EU)
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Preis
Menge
5mg
R131741-5mg
Auf Bestellung · 8–12 Wochen
130,07€
10mg
R131741-10mg
—
2 Auf Lager
199,49€
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Warum diese Qualität

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

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Lagerung & Versand

Protected from light,Store at -20°C Versand Ice chest + Ice pads. Genaue Spezifikationen finden Sie im chargenspezifischen COA.

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Qualitätsdokumente

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

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Literaturbeleg

In 0 peer-reviewten Publikationen zu Chromatographie, organischer Synthese und Kreuzkupplungsreaktionen zitiert.

Übersicht

L-Sulforaphane, a compound found at high levels in broccoli, has been reported to prevent NFκB binding, which results in downregulation of apoptosis inhibitors therefore inducing apoptosis. Research has demonstrated sulforaphane to be a potent inducer of phase II detoxification enzymes and display chemoprotective properties. Other experiments have shown sulforaphane to induce enzymes of xenobiotic metabolism and therefore accelerate the metabolic disposal of xenobiotics. Sulforaphane also displays a capacity to inhibit intracellular, extracellular, and antibiotic-resistant strains of Helicobacter pylori. Additionally, this compound has been found to prevent clonogenicity. This product is sold in the L-enantiomer form.
An inducer of apoptosis, detoxification and xenobiotic enzymes

Spezifikationen

Synonyme
HY-13755A | 1-isothiocyanato-4-[(R)-methanesulfinyl]butane | 1-Propanamine, 2-chloro-N,N-dimethyl-, hydrochloride (1:1) | (R)-1-Isothiocyanato-4-(methylsulfinyl)butane | GA49J4310U | 2-Piperidinemethanol, 97% | SULFORAPHANE [MI] | SULFORAPHANE [INCI] | (R
Spezifikationen & Reinheit
Moligand™, ≥98%
Biochemische und physiologische Mechanismen
Non-competitive antagonist of the aryl hydrocarbon receptor. Natural isothiocyanate. Antioxidant, promotes cell proliferation, reduces senescence and apoptosis. Upregulates CYP1A1/1B1 apoprotein levels in vivo . Chemopreventive.
Storage
Protected from light,Store at -20°C
Verschickt in
Ice chest + Ice pads
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Note
Moligand™
Aktionsart
INHIBITOR
Hinweis
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Reinheit
≥98%
Namen und Kennungen
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/528753261
Kanonisches Lächeln
CS(=O)CCCCN=C=S
IUPAC Name
1-isothiocyanato-4-[(R)-methylsulfinyl]butane
InChIKey
SUVMJBTUFCVSAD-SNVBAGLBSA-N
INCHI
1S/C6H11NOS2/c1-10(8)5-3-2-4-7-6-9/h2-5H2,1H3/t10-/m1/s1
Isomere SMILES
C[S@@](=O)CCCCN=C=S
WGK Deutschland
3
Molekulargewicht
177.29
Reaxy-Rn
1723237
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1723237&ln=

Dokumentation

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Erweiterte Daten

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganosulfur compounds
KlasseSulfoxides
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentSulfoxides
Alternative Parents Isothiocyanates  Sulfinyl compounds  Propargyl-type 1,3-dipolar organic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Sulfoxide - Isothiocyanate - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Sulfinyl compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Aliphatic acyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as sulfoxides. These are compounds containing a sulfoxide functional group, with the structure RS(=O)R' (R,R' not H).
External Descriptors sulforaphane
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (menschlich)
NFE2L2 Tchem Nuclear factor erythroid 2-related factor 2 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MRC5 (9203 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HaCaT (4069 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Zugehörige Ziele (nicht menschlich)
Nqo1 NAD(P)H dehydrogenase [quinone] 1 (1058 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

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3 results found

Lot NumberCertificate TypeDatumArtikel
F1515081F1515081Certificate of AnalysisJul 07, 2026 R131741
L2529243L2529243Certificate of AnalysisDec 15, 2025 R131741
F2524554F2524554Certificate of AnalysisJun 10, 2025 R131741
Chemische und physikalische Eigenschaften
LöslichkeitSoluble in DMSO (>5 mg/ml), 100% ethanol, methanol, chloroform, and ethyl acetate.
Empfindlichkeitlight sensitive
Molekulargewicht177.300 g/mol
XLogP31.400
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count4
Rotatable Bond Count5
Exact Mass177.028 Da
Monoisotopic Mass177.028 Da
Topological Polar Surface Area80.700 Ų
Heavy Atom Count10
Formal Charge0
Complexity152.000
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
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Lösungsrechner
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