Ochromycinone (STA-21) - ≥98% , CAS No.111540-00-2

CAS: 111540-00-2 Cat. No.: O413885 Summenformel: C19H14O4 Molekulargewicht: 306.31
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GRADE & PURITY ≥98%
Synonyms
HY-18061 | NSC628869 | NSC-628869 | 8-hydroxy-3-methyl-3,4-dihydrotetraphene-1,7,12(2H)-trione | AKOS032945165 | Benz[a]anthracene-1,12-trione, 1,2,3,4,7,12-hexahydro-8-hydroxy-3-methyl- | FT-0673176 | CCG-267534 | {Benz[a]anthracene-1,7,12-trione,} 1,2,3
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
★
Size
Deutschland (EU)
USA*
Price
Qty
1mg
O413885-1mg
Auf Bestellung · 8–12 Wochen

26,81€

40,70€
Speichern 13,88 € (34.12%)
5mg
O413885-5mg
Auf Bestellung · 8–12 Wochen

97,97€

147,43€
Speichern 49,46 € (33.55%)
10mg
O413885-10mg
—
2 Auf Lager

137,02€

205,57€
Speichern 68,55 € (33.35%)
25mg
O413885-25mg
—
1 Auf Lager

300,15€

450,27€
Speichern 150,12 € (33.34%)
50mg
O413885-50mg
—
1 Auf Lager

539,65€

809,51€
Speichern 269,87 € (33.34%)
100mg
O413885-100mg
Auf Bestellung · 8–12 Wochen

971,78€

1.457,71€
Speichern 485,93 € (33.34%)
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Why this grade

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

🌡

Storage & shipping

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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

Application:

STA-21 has been used as a signal transducer and activator of transcription 3 (STAT3) inhibitor to study its effects on glioblastoma and primary glioblastoma cells. It has also been used as a STAT3 dimerization inhibitor to study its effects on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) production in human lung cancer cell line.


Information

Ochromycinone (STA-21) is a selectiveSTAT3inhibitor.


Targets

STAT3


In vitro

In cells, STA-21 inhibits Stat3 DNA binding activity, Stat3 dimerization, and Stat3-dependent luciferase activity. STA-21 remarkably inhibits the growth and the survival of the breast carcinoma cells MDA-MB-231, MDA-MB-435s, and MDA-MB-468 that express persistently activated Stat3. In RH30 and RD2 cells, STA-21 also inhibits cell viability and growth and induced apoptosis through caspases 3, 8 and 9 pathways.


In vivo

In IL-1Ra–KO mice, STA-21 (0.5 mg/kg, i.p.) reduces the arthritis score and the incidence of arthritis by decreasing the proportion of Th17 cells and increasing the proportion of Treg cells expressing FoxP3.


Cell Research(from reference)

Cell lines:MDA-MB-231, MDA-MB-435s, MDA-MB-453, MDA-MB-468, MCF7, and Caov-3 cells 

Concentrations:20 or 30 μM 

Incubation Time:48 h 

Specifications

Synonyme
HY-18061 | NSC628869 | NSC-628869 | 8-hydroxy-3-methyl-3,4-dihydrotetraphene-1,7,12(2H)-trione | AKOS032945165 | Benz[a]anthracene-1,12-trione, 1,2,3,4,7,12-hexahydro-8-hydroxy-3-methyl- | FT-0673176 | CCG-267534 | {Benz[a]anthracene-1,7,12-trione,} 1,2,3
Spezifikationen & Reinheit
≥98%
Biochemische und physiologische Mechanismen
Ochromycinone (STA-21) is a selective STAT3 inhibitor.
Storage
Store at -20°C
Verschickt in
Ice chest + Ice pads
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Aktionsart
INHIBITOR
Reinheit
≥98%
Namen und Kennungen
Pubchem Sid504758592
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504758592
Kanonisches LächelnCC1CC2=C(C(=O)C1)C3=C(C=C2)C(=O)C4=C(C3=O)C=CC=C4O
IUPAC Name8-hydroxy-3-methyl-3,4-dihydro-2H-benzo[a]anthracene-1,7,12-trione
InChIKeyZAWXOCUFQSQDJS-UHFFFAOYSA-N
INCHI1S/C19H14O4/c1-9-7-10-5-6-12-17(15(10)14(21)8-9)19(23)11-3-2-4-13(20)16(11)18(12)22/h2-6,9,20H,7-8H2,1H3
Isomere SMILES CC1CC2=C(C(=O)C1)C3=C(C=C2)C(=O)C4=C(C3=O)C=CC=C4O
Molekulargewicht 306.31
Reaxy-Rn 3121949
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3121949&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
SuperclassPhenylpropanoids and polyketides
KlasseAngucyclines
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentAngucyclines
Alternative Parents Anthraquinones  Phenanthrenes and derivatives  Tetralins  Aryl alkyl ketones  1-hydroxy-4-unsubstituted benzenoids  1-hydroxy-2-unsubstituted benzenoids  Vinylogous acids  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents Angucycline core - 9,10-anthraquinone - Anthraquinone - Anthracene - Phenanthrene - Tetralin - Aryl alkyl ketone - Aryl ketone - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Vinylogous acid - Ketone - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Aromatic homopolycyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as angucyclines. These are polyketides with a structure based on then benz[a]anthracene skeleton, with the particularity that the central ring of the anthracene moiety is a para-quinone.
External Descriptors Not available
3D-Struktur
Interaktives chemisches Strukturmodell





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Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
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.

10 results found

Lot NumberCertificate TypeDatumArtikel
E2625134Certificate of AnalysisJun 04, 2026 O413885
F2507080Certificate of AnalysisJun 25, 2025 O413885
F2229515Certificate of AnalysisApr 03, 2025 O413885
F2229516Certificate of AnalysisApr 03, 2025 O413885
F2229517Certificate of AnalysisApr 03, 2025 O413885
F2229518Certificate of AnalysisJul 15, 2022 O413885
F2229001Certificate of AnalysisJun 05, 2022 O413885
F2229002Certificate of AnalysisJun 05, 2022 O413885
F2229003Certificate of AnalysisJun 05, 2022 O413885
F2229004Certificate of AnalysisJun 05, 2022 O413885
Chemische und physikalische Eigenschaften
LöslichkeitSolubility (25°C) In vitro DMSO: 21 mg/mL (68.55 mM); Ethanol: 2 mg/mL (6.52 mM); Water: Insoluble;
Molekulargewicht306.300 g/mol
XLogP33.600
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count4
Rotatable Bond Count0
Exact Mass306.089 Da
Monoisotopic Mass306.089 Da
Topological Polar Surface Area71.400 Ų
Heavy Atom Count23
Formal Charge0
Complexity554.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
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Häufig gestellte Fragen

What is the purity of this product?
This product is supplied at ≥98% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.
How should this product be stored?
Store at ?20 °C. Freezer storage is required to maintain the specified shelf life.
How is this product shipped?
This product ships in an insulated container with ice pads. 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 111540-00-2, the molecular formula is C19H14O4, and the molecular weight is 306.31 g/mol. InChIKey ZAWXOCUFQSQDJS-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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