Ro 48-8071 - ≥98% , CAS No.189197-69-1

CAS: 189197-69-1 Cat. No.: R276229 Formula: C27H31BrFNO6 Peso molecolare: 564.4
Disponibile su ordine
GRADE & PURITY ≥98%
Synonyms
SCHEMBL4437311 | SR-05000001957 | Methanone, (4-bromophenyl)[2-fluoro-4-[[6-(methyl-2-propen-1-ylamino)hexyl]oxy]phenyl]-, (2E)-2-butenedioate (1:1) | C27H31BrFNO6 | Ro-48-8071 fumarate | Ro48-8071 fumarate | EX-A532 | A14321 | (4-bromophenyl)-[2-fluoro-4
Storage
Protected from light,Store at -20°C
Shipped In
Ice chest + Ice pads
★
Size
Germania (EU)
USA*
Price
Qty
10mg
R276229-10mg
Su ordinazione · 8–12 settimane

54,58€

82,35€
Salva 27,77 € (33.72%)
25mg
R276229-25mg
—
1 Disponibile

91,89€

137,88€
Salva 45,99 € (33.35%)
50mg
R276229-50mg
—
1 Disponibile

154,37€

231,60€
Salva 77,23 € (33.35%)
100mg
R276229-100mg
—
2 Disponibile

261,97€

393,00€
Salva 131,03 € (33.34%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Panoramica

An   benzofuranylallylamine compound that acts as a potent, active site targeting, competitive and reversible inhibitor of 2,3-oxidosqualene:lanosterol cyclase activity (OSC; IC50 ~6.5 nM against mammalian) and reduces cholesterol synthesis (IC50 ~1.5 nM in HepG2 cells) with minimal buildup of both dioxidosqualene and monooxidosqualene. Downregulates 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase mRNA and synthesis, and exerts less adverse effects in animal models than Statins. Shown to preferentially enhance the DNA-binding affinity of mutant p53 and arrest the growth of human breast cancer cells (IC50 ~10 µM).

Specifications

Sinonimi
SCHEMBL4437311 | SR-05000001957 | Methanone, (4-bromophenyl)[2-fluoro-4-[[6-(methyl-2-propen-1-ylamino)hexyl]oxy]phenyl]-, (2E)-2-butenedioate (1:1) | C27H31BrFNO6 | Ro-48-8071 fumarate | Ro48-8071 fumarate | EX-A532 | A14321 | (4-bromophenyl)-[2-fluoro-4
Specifiche e purezza
≥98%
Meccanismi biochimici e fisiologici
Potent 2,3-oxidosqualene cyclase (OSC) inhibitor (IC 50 = 6.5 nM). Displays lipid lowering activity. Active in vivo .
Condizioni di conservazione di stoccaggio
Protected from light,Store at -20°C
Spedito in
Ice chest + Ice pads
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Nota
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.
Purezza
≥98%
Nomi e identificatori
Pubchem Sid528766963
Sorrisi canoniciCN(CCCCCCOC1=CC(=C(C=C1)C(=O)C2=CC=C(C=C2)Br)F)CC=C.C(=CC(=O)O)C(=O)O
IUPAC Name(4-bromophenyl)-[2-fluoro-4-[6-[methyl(prop-2-enyl)amino]hexoxy]phenyl]methanone;(E)-but-2-enedioic acid
InChIKeyXCYAYLWZCRGKDS-WLHGVMLRSA-N
INCHI1S/C23H27BrFNO2.C4H4O4/c1-3-14-26(2)15-6-4-5-7-16-28-20-12-13-21(22(25)17-20)23(27)18-8-10-19(24)11-9-18;5-3(6)1-2-4(7)8/h3,8-13,17H,1,4-7,14-16H2,2H3;1-2H,(H,5,6)(H,7,8)/b;2-1+
Isomeri SMILES CN(CCCCCCOC1=CC(=C(C=C1)C(=O)C2=CC=C(C=C2)Br)F)CC=C.C(=C/C(=O)O)\C(=O)O
CAS alternativo 161582-11-2
Peso molecolare 564.4

Documentazione

📋 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
SuperclassBenzenoids
ClasseBenzene and substituted derivatives
SubclassBenzophenones
Intermediate Tree Nodes Not available
Direct ParentBenzophenones
Alternative Parents Aryl-phenylketones  Diphenylmethanes  Benzoyl derivatives  Phenoxy compounds  Phenol ethers  Alkyl aryl ethers  Bromobenzenes  Fluorobenzenes  Aryl fluorides  Dicarboxylic acids and derivatives  Aryl bromides  Unsaturated fatty acids  Vinylogous halides  Trialkylamines  Carboxylic acids  Organic oxides  Hydrocarbon derivatives  Organobromides  Organofluorides  Organopnictogen compounds  
Molecular FrameworkNot available
Substituents Benzophenone - Diphenylmethane - Aryl-phenylketone - Benzoyl - Phenol ether - Aryl ketone - Phenoxy compound - Bromobenzene - Alkyl aryl ether - Fluorobenzene - Halobenzene - Fatty acyl - Fatty acid - Unsaturated fatty acid - Dicarboxylic acid or derivatives - Aryl bromide - Aryl halide - Aryl fluoride - Vinylogous halide - Tertiary aliphatic amine - Tertiary amine - Ketone - Carboxylic acid derivative - Ether - Carboxylic acid - Organic nitrogen compound - Organohalogen compound - Organobromide - Organofluoride - Carbonyl group - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Amine - Aromatic homomonocyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as benzophenones. These are organic compounds containing a ketone attached to two phenyl groups.
External Descriptors Not available
Struttura 3D
Modello di struttura chimica interattiva





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Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Obiettivi associati (non umani)
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Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
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.

4 results found

Lot NumberCertificate TypeDataOggetto
F2205177Certificate of AnalysisMar 13, 2026 R276229
F2205182Certificate of AnalysisMar 13, 2026 R276229
F2205535Certificate of AnalysisMar 13, 2026 R276229
F2205547Certificate of AnalysisMar 13, 2026 R276229
Proprietà chimiche e fisiche
SolubilitàSoluble in water to 25 mM
SensibilitàSensitive to light and humidity
Peso molecolare564.400 g/mol
XLogP3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count8
Rotatable Bond Count14
Exact Mass563.132 Da
Monoisotopic Mass563.132 Da
Topological Polar Surface Area104.000 Ų
Heavy Atom Count36
Formal Charge0
Complexity586.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds1
Covalently-Bonded Unit Count2
Citations of This Product
Riferimenti
1. Yuxiang Hong, Yang Gu, Dewei Lin, Zizhao Wu, Wenhao Chen, Tianjian Lu, Pornpatsorn Lertphadungkit, Jingbo Ma, Haili Wang, Bo Zhou, Gil Bar-Sela, Idan Cohen, Peng Xu.  (2025)  De novo biosynthesis of cannabinoid and its analogs in Yarrowia lipolytica.  BioDesign Research,      [PMID:41416103] [10.1016/j.bidere.2025.100021]
Calcolatori di soluzioni
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