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(R)-Sulforaphane - 98%, high purity , CAS No.142825-10-3

In stock
Item Number
R131741
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SKU Size
Availability
Price Qty
R131741-10mg
10mg
2
$282.90

Non-competitive antagonist of the Ah receptor

Basic Description

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
Specifications & Purity Moligand™, ≥98%
Biochemical and Physiological Mechanisms 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 Temp Protected from light,Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Grade Moligand™
Note 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.
Product Description

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

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organosulfur compounds
Class Sulfoxides
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Sulfoxides
Alternative Parents Isothiocyanates  Sulfinyl compounds  Propargyl-type 1,3-dipolar organic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aliphatic 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
Description This 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

Associated Targets(Human)

NFE2L2 Tchem Nuclear factor erythroid 2-related factor 2 (1 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
VDR Tclin Vitamin D receptor (26531 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MRC5 (9203 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
A549 (127892 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HaCaT (4069 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Nqo1 NAD(P)H dehydrogenase [quinone] 1 (1058 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name 1-isothiocyanato-4-[(R)-methylsulfinyl]butane
INCHI InChI=1S/C6H11NOS2/c1-10(8)5-3-2-4-7-6-9/h2-5H2,1H3/t10-/m1/s1
InChIKey SUVMJBTUFCVSAD-SNVBAGLBSA-N
Smiles CS(=O)CCCCN=C=S
Isomeric SMILES C[S@@](=O)CCCCN=C=S
WGK Germany 3
Molecular Weight 177.29
Reaxy-Rn 1723237
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1723237&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

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.

1 results found

Lot Number Certificate Type Date Item
F1515081 Certificate of Analysis Jan 25, 2023 R131741

Chemical and Physical Properties

Solubility Soluble in DMSO (>5 mg/ml), 100% ethanol, methanol, chloroform, and ethyl acetate.
Sensitivity light sensitive
Molecular Weight 177.300 g/mol
XLogP3 1.400
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 5
Exact Mass 177.028 Da
Monoisotopic Mass 177.028 Da
Topological Polar Surface Area 80.700 Ų
Heavy Atom Count 10
Formal Charge 0
Complexity 152.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 1
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

Solution Calculators

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