Home Shop R,S-Sulforaphane

R,S-Sulforaphane

ALX-350-232

Datasheet
Manual
SDS
CofA

Already have an account?

Carcinogenesis inhibitor

R,S-Sulforaphane is a synthetic version of the naturally occurring compound, R-sulforaphane, from Broccoli. It is a racemic mixture of both the R and S isomers.
Potent, selective inducer of phase II detoxification enzymes. Inhibits chemically induced mammary tumor formation in rats. Inhibits LPS-induced HMGB1 (high mobility group box 1) secretion.

Shipping: Available products typically ship within 24/48h, via priority shipping.

Do you need support? Contact Customer Service or Technical Support.

Online Account
Access or Create Your Account

Product Details

Alternative Name	D,L-Sulforaphane, 1-Isothiocyanato-4-methylsulfinyl-butane
Appearance	Slightly yellowish liquid.
CAS	4478-93-7 (unspecified stereo)
Formula	C₆H₁₁NOS₂
Identity	Identity determined by 1H-NMR and MS.
MI	14: 8962
MW	177.3
Purity	≥98% (UHPLC)
Solubility	Soluble in methanol or DMSO.
Source	Synthetic.

Handling & Storage

Use/Stability	As indicated on product label or CoA when stored as recommended.
Long Term Storage	-20°C
Shipping	Ambient Temperature

Regulatory Status	RUO – Research Use Only

Dietary Antioxidants Significantly Attenuate Hyperoxia-Induced Acute Inflammatory Lung Injury by Enhancing Macrophage Function via Reducing the Accumulation of Airway HMGB1: Patel, V., Dial, K., et al.; Int. J. Mol. Sci. 21, (2020), Abstract
Free light chains injure proximal tubule cells through the STAT1/HMGB1/TLR axis: Upadhyay, R., Ying, W. Z., et al.; JCI Insight 5, (2020), Abstract
Simultaneous quantification of sulforaphene and sulforaphane by reverse phase HPLC and their content in Raphanus sativus L. var. caudatus Alef extracts: S. Sangthong, et al.; Food. Chem. 201, 139 (2016), Application(s): Standard, Abstract
Flavokawains A and B from kava (Piper methysticum) activate heat shock and antioxidant responses and protect against hydrogen peroxide-induced cell death in HepG2 hepatocytes: Pinner, K. D., Wales, C. T., et al.; Pharm. Biol. 54, 1503 (2016), Abstract
Synergy between sulforaphane and selenium in protection against oxidative damage in colonic CCD841 cells: Y. Wang, et al.; Nutr. Res. 35, 610 (2015), Abstract
4-Methylthiobutyl isothiocyanate (Erucin) from rocket plant dichotomously affects the activity of human immunocompetent cells: C. Gründemann, et al.; Phytomedicine 22, 369 (2015), Application(s): Gas Chromatography – Mass Spectrometry , Abstract
Protective effect of sulforaphane against oxidative stress: Recent advances: C.E. Guerrero-Beltran, et al.; Exp. Toxicol. Pathol. 64, 503 (2012), Abstract
Sulforaphane targets pancreatic tumor-initiating cells by NF-{kappa}B-induced anti-apoptotic signaling: G. Kallifatidis, et al.; Gut 58, 949 (2009), Abstract
The phase 2 enzyme inducers ethacrynic acid, DL-sulforaphane, and oltipraz inhibit lipopolysaccharide-induced high-mobility group box 1 secretion by RAW 264.7 cells: M.E. Killeen, et al.; J. Pharmacol. Exp. Ther. 316, 1070 (2006), Abstract
A novel mechanism of chemoprotection by sulforaphane: inhibition of histone deacetylase: M.C. Myzak, et al.; Cancer Res. 64, 5767 (2004), Abstract — Full Text

Related Products

(+)-Catechin . monohydrate

ALX-385-017

Free radical scavenger

10 citations

Alternative Name	(+)-3,3’,4’,5,7-Flavanpentol . H2O
CAS	225937-10-0
Purity	≥98% (HPLC)

(-)-Arctigenin

ALX-350-312

Antitumor agent

9 citations

Alternative Name	(3R,4R)-4-[(3,4-Dimethoxyphenyl)methyl]dihydro-3-[(4-hydroxy-3-methoxyphenyl)methyl]-2-(3H)-furanone
CAS	7770-78-7
Couple Type	Inhibitor
Purity	≥97% (HPLC)

(-)-Arctiin

ALX-350-318

Antitumor agent

8 citations

Alternative Name	(3R,4R)-4-[(3,4-Dimethoxyphenyl)methyl]-3-[[4-(β-D-glucopyranosyloxy)-3-methoxyphenyl]methyl]dihydro-2(3H)-furanone
CAS	20362-31-6
Couple Type	Inhibitor
Purity	≥95% (HPLC)

(-)-Epigallocatechin gallate

ALX-270-263

Inhibitor of NOS, telomerase and Dnmt

36 citations

Alternative Name	EGCG, (2R,3R)-2-(3,4,5-Trihydroxyphenyl)-3,4-dihydro-1[2H]-benzopyran-3,5,7-triol 3-(3,4,5-trihydroxybenzoate)
CAS	989-51-5
Couple Type	Inhibitor
Purity	≥98% (HPLC)

Last modified: May 29, 2024

Datasheet, Manuals, SDS & CofA

Manuals And Inserts

Datasheet

Certificate of Analysis

Please enter the lot number as featured on the product label

Lot No. :

SDS

Enzo Life Science provides GHS Compliant SDS

If your language is not available please fill out the SDS request form

Your Cart

Your Cart

R,S-Sulforaphane

ALX-350-232

Product Details

Handling & Storage

Datasheet, Manuals, SDS & CofA

Manuals And Inserts

Certificate of Analysis

SDS

Change Country

Tell us about You

Tell us about your paper

Tell us about You

Tell us about your project