Emodine - ≥90%(HPLC) , CAS No.518-82-1

CAS: 518-82-1 Cat. No.: E106692 Formule: C15H10O5 Poids moléculaire: 270.24 Numéro CE: 208-258-8
DISPONIBLE À COMMANDE
GRADE & PURITY ≥90%(HPLC)
Synonyms
EMO | Frangula emodin | MEGxp0_000460 | 1,3,8-Trihydroxy-6-methylanthraquinone | C.I. Natural Yellow 14 | Lopac-E-7881 | Anthraquinone,3,8-trihydroxy-6-methyl- | BDBM11318 | KBio2_005068 | SR-01000075615 | EMODIN [USP-RS] | rheum emodium | 1f0q | 3bqc | 3
Storage
A conserver entre 2 et 8°C
Shipped In
Glace humide
★
Size
Allemagne (EU)
USA*
Price
Qty
100mg
E106692-100mg
—
3 En stock
12,93€
250mg
E106692-250mg
—
3 En stock
13,80€
500mg
E106692-500mg
—
2 En stock
24,21€
1g
E106692-1g
—
1 En stock
41,56€
5g
E106692-5g
—
5 En stock
129,21€
10g
E106692-10g
Sur commande · 8–12 semaines
218,58€
25g
E106692-25g
—
1 En stock
366,97€
Enter a quantity for the sizes you want to add.
🧪
Why this grade

≥90%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

A conserver entre 2 et 8°C Ships Glace humide 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 65 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Vue d’ensemble

Un puissant inhibiteur de la tyrosine kinase p56lck dont il a été démontré qu'il supprime l'activité de la tyrosine kinase HER2/neu.

Specifications

Synonymes
EMO | Frangula emodin | MEGxp0_000460 | 1,3,8-Trihydroxy-6-methylanthraquinone | C.I. Natural Yellow 14 | Lopac-E-7881 | Anthraquinone,3,8-trihydroxy-6-methyl- | BDBM11318 | KBio2_005068 | SR-01000075615 | EMODIN [USP-RS] | rheum emodium | 1f0q | 3bqc | 3
Spécifications et pureté
≥90%(HPLC)
Mécanismes biochimiques et physiologiques
L'émodine est un puissant inhibiteur de Lck (p56lck tyrosine kinase) (IC50 = 18,5 μM). Il bloque sélectivement la croissance des cellules épithéliales bronchiques humaines transformées par v-ras (IC50 = 15 μM). Il a été démontré que l'émodine supprime l'a
Conditions de stockage de stockage
A conserver entre 2 et 8°C
Expédié en
Glace humide
Note
Besoin de plus de conseils sur la solubilité, l'utilisation et la manipulation ? Veuillez consulter notre page de questions fréquemment posées (FAQ) pour plus de détails.
Pureté
≥90%(HPLC)
Noms et identifiants
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488179752
Sourires canoniques
CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O
IUPAC Name
1,3,8-trihydroxy-6-methylanthracene-9,10-dione
InChIKey
RHMXXJGYXNZAPX-UHFFFAOYSA-N
INCHI
1S/C15H10O5/c1-6-2-8-12(10(17)3-6)15(20)13-9(14(8)19)4-7(16)5-11(13)18/h2-5,16-18H,1H3
Isomères SMILES
CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O
Poids moléculaire
270.24
Reaxy-Rn
1888141
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1888141&ln=

Documentation

📋 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
ClasseAnthracenes
SubclassAnthraquinones
Intermediate Tree Nodes Not available
Direct ParentHydroxyanthraquinones
Alternative Parents Aryl ketones  1-hydroxy-4-unsubstituted benzenoids  1-hydroxy-2-unsubstituted benzenoids  Vinylogous acids  Polyols  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents Hydroxyanthraquinone - Aryl ketone - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Vinylogous acid - Ketone - Polyol - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homopolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as hydroxyanthraquinones. These are compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group.
External Descriptors Anthracenes and phenanthrenes
Structure 3D
Modèle de structure chimique interactif





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PSMB1 Tclin Proteasome subunit beta type-1 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
MGAM Tclin Maltase-glucoamylase (654 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
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NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
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AR Tclin Androgen Receptor (11781 Activities)
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VDR Tclin Vitamin D receptor (26531 Activities)
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TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
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MAOA Tclin Monoamine oxidase A (11911 Activities)
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ACHE Tclin Acetylcholinesterase (18204 Activities)
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MAOB Tclin Monoamine oxidase B (8835 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTH1R Tclin Parathyroid hormone receptor (47172 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ESR2 Tclin Estrogen receptor beta (9272 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
P2RY12 Tclin Purinergic receptor P2Y12 (2369 Activities)
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ELANE Tclin Leukocyte elastase (8173 Activities)
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AKR1B1 Tclin Aldose reductase (1404 Activities)
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THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
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RXRA Tclin Retinoid X receptor alpha (3637 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NPC1L1 Tclin Niemann-Pick C1-like protein 1 (346 Activities)
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CXCL8 Tchem Interleukin-8 (642 Activities)
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MAPK11 Tchem MAP kinase p38 beta (2785 Activities)
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LCK Tclin Tyrosine-protein kinase LCK (9212 Activities)
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CYP1B1 Tchem Cytochrome P450 1B1 (1148 Activities)
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MAPK14 Tchem MAP kinase p38 alpha (12866 Activities)
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POLB Tchem DNA polymerase beta (23632 Activities)
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SRC Tclin Tyrosine-protein kinase SRC (10310 Activities)
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CTSG Tchem Cathepsin G (2304 Activities)
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PRKAA2 Tchem AMP-activated protein kinase, alpha-2 subunit (1328 Activities)
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PIM1 Tchem Serine/threonine-protein kinase PIM1 (9629 Activities)
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CSK Tchem Tyrosine-protein kinase CSK (2395 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RPS6KA5 Tchem Ribosomal protein S6 kinase alpha 5 (3355 Activities)
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SYK Tclin Tyrosine-protein kinase SYK (7372 Activities)
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PLK1 Tchem Serine/threonine-protein kinase PLK1 (28605 Activities)
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RPS6KA1 Tchem Ribosomal protein S6 kinase alpha 1 (2796 Activities)
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MAPK13 Tchem MAP kinase p38 delta (2605 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAPKAPK2 Tchem MAP kinase-activated protein kinase 2 (4814 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAPKAPK5 Tchem MAP kinase-activated protein kinase 5 (2831 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A1 Tchem Cytochrome P450 1A1 (1169 Activities)
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ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
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ROCK2 Tclin Rho-associated protein kinase 2 (6206 Activities)
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NR1H4 Tclin Bile acid receptor FXR (6228 Activities)
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AKR1A1 Tchem Aldehyde reductase (91 Activities)
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Man1 Alpha-mannosidase (188 Activities)
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Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
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.

25 results found

Lot NumberCertificate TypeDateArticle
J2608038Certificate of AnalysisOct 14, 2026 E106692
H2615134Certificate of AnalysisApr 27, 2026 E106692
D2623841Certificate of AnalysisApr 27, 2026 E106692
H2501008Certificate of AnalysisAug 05, 2025 E106692
H2119123Certificate of AnalysisJun 09, 2025 E106692
H2119122Certificate of AnalysisJun 09, 2025 E106692
H2322017Certificate of AnalysisAug 28, 2023 E106692
F1515102Certificate of AnalysisMar 08, 2023 E106692
B2303380Certificate of AnalysisFeb 10, 2023 E106692
H2515027Certificate of AnalysisFeb 10, 2023 E106692
H2501112Certificate of AnalysisFeb 10, 2023 E106692
E2620015Certificate of AnalysisFeb 10, 2023 E106692
B2303428Certificate of AnalysisFeb 10, 2023 E106692
B2303393Certificate of AnalysisFeb 10, 2023 E106692
B2303392Certificate of AnalysisFeb 10, 2023 E106692
B2303390Certificate of AnalysisFeb 10, 2023 E106692
B2303388Certificate of AnalysisFeb 10, 2023 E106692
B2303387Certificate of AnalysisFeb 10, 2023 E106692
B2303379Certificate of AnalysisFeb 10, 2023 E106692
K2203210Certificate of AnalysisNov 05, 2022 E106692
J1818077Certificate of AnalysisAug 10, 2022 E106692
J1818079Certificate of AnalysisAug 10, 2022 E106692
E2522027Certificate of AnalysisAug 27, 2021 E106692
B2422034Certificate of AnalysisAug 27, 2021 E106692
K2425050Certificate of AnalysisAug 27, 2021 E106692
Propriétés chimiques et physiques
SolubilitéSoluble in ethanol, sodium carbonate solution, DMSO (1 mg/ml), aqueous alkali, 1eq. NaOH (100 mM), ammonium hydroxide (10 mg/ml), ether, chloroform, benzene , and THF. Insoluble in water.
SensibilitéLight,Air sensitive
Point de fusion (°C)256-257°C
Poids moléculaire270.240 g/mol
XLogP32.700
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count5
Rotatable Bond Count0
Exact Mass270.053 Da
Monoisotopic Mass270.053 Da
Topological Polar Surface Area94.800 Ų
Heavy Atom Count20
Formal Charge0
Complexity434.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
FAQ et articles
Citations of This Product
Calculateurs de solution
Avis

Avis des clients

Foire aux questions

What is the purity of this product, and how is it determined?
This product is supplied at ≥90% purity, determined by HPLC. Lot-specific values are stated on the Certificate of Analysis.
How should this product be stored?
Store at 2–8 °C. Refrigerated storage is required to maintain the specified shelf life.
How is this product shipped?
This product ships chilled on wet ice. Unpack on arrival and transfer it to the storage condition stated above.
What are the CAS number, molecular formula and molecular weight?
The CAS Number is 518-82-1, the molecular formula is C15H10O5, and the molecular weight is 270.24 g/mol. InChIKey RHMXXJGYXNZAPX-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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