Costundide - Moligand™, ≥97% , CAS No.553-21-9

CAS: 553-21-9 Cat. No.: C139779 Summenformel: C15H20O2 Molekulargewicht: 232.32 EG-Nummer: 683-148-4
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QUALITÄT & REINHEIT Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥97%
Synonyms
MFCD00210262 | HMS3677B19 | Costunlide | NSC106404 | Cyclodeca[b]furan-2(3H)-one, 3a,4,5,8,9,11a-hexahydro-6,10-dimethyl-3-methylene-, (3aS,6E,10E,11aR)- | AKOS015969714 | Costunolide | SCHEMBL92714 | (3aS,6E,10E,11aR)-6,10-dimethyl-3-methylidene-3a,4,5,8
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
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Preis
Menge
5mg
C139779-5mg
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3 Auf Lager
17,27€
25mg
C139779-25mg
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3 Auf Lager
51,98€
100mg
C139779-100mg
Auf Bestellung · 8–12 Wochen
100,57€
500mg
C139779-500mg
Auf Bestellung · 8–12 Wochen
347,01€
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Warum diese Qualität

Moligand™, ≥97% Moligand™ für empfindliche chromatographische und analytische Workflows, die minimale Basislinieninterferenzen erfordern.

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Lagerung & Versand

Store at -20°C Versand Ice chest + Ice pads. Genaue Spezifikationen finden Sie im chargenspezifischen COA.

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Qualitätsdokumente

SDS, COA, Datenblatt und Spezifikationsblatt stehen zum Download bereit. Chargenspezifische COA über Chargennummernsuche abrufbar.

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Literaturbeleg

In 2 peer-reviewten Publikationen zu Chromatographie, organischer Synthese und Kreuzkupplungsreaktionen zitiert.

Übersicht

Costunolide is a sesquiterpene lactone isolated from Magnolia sieboldii. The compound is described to act as an antioxidant, anti-mycobacterial, anti-inflammatory, and anti-viral, with cytotoxic activity. Additionally, Costunolide is reported to inhibit the activity of TERT (telomerase). Studies indicate that Costunolide activates JNK downstream of ROS in leukemia cells, and upstream of Bcl-2. The compound has also been suggested to act as an inhibitor of NOS (nitric oxide synthase) and the VEGFR KDR/Flk-1 signaling pathway
A sequiterpene lactone that inhibits telomerase

Spezifikationen

Synonyme
MFCD00210262 | HMS3677B19 | Costunlide | NSC106404 | Cyclodeca[b]furan-2(3H)-one, 3a,4,5,8,9,11a-hexahydro-6,10-dimethyl-3-methylene-, (3aS,6E,10E,11aR)- | AKOS015969714 | Costunolide | SCHEMBL92714 | (3aS,6E,10E,11aR)-6,10-dimethyl-3-methylidene-3a,4,5,8
Spezifikationen & Reinheit
Moligand™, ≥97%
Biochemische und physiologische Mechanismen
Description:IC50 Value: 6.2 - 9.8 ?g/mL(sarcoma cells viability)[3]Costunolide, a sesquiterpene lactone, exhibits anti-inflammatory and anti-oxidant properties and mediates apoptosis.in vitro: Costunolide significantly inhibited RANKL-induced BMM differen
Storage
Store at -20°C
Verschickt in
Ice chest + Ice pads
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Note
Moligand™
Hinweis
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.
Reinheit
≥97%
Namen und Kennungen
Pubchem Sid
Kanonisches Lächeln
CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C
IUPAC Name
(3aS,6E,10E,11aR)-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one
InChIKey
HRYLQFBHBWLLLL-AHNJNIBGSA-N
INCHI
1S/C15H20O2/c1-10-5-4-6-11(2)9-14-13(8-7-10)12(3)15(16)17-14/h5,9,13-14H,3-4,6-8H2,1-2H3/b10-5+,11-9+/t13-,14+/m0/s1
Isomere SMILES
C/C/1=C\CC/C(=C/[C@@H]2[C@@H](CC1)C(=C)C(=O)O2)/C
WGK Deutschland
3
RTECS
LY4270000
Molekulargewicht
232.32
Reaxy-Rn
22984848
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=22984848&ln=

Dokumentation

📋 Sicherheitsdatenblatt (SDS)

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✅ Analysezertifikat (COA)

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📊 Datenblatt

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🔬 Spezifikationsblatt

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Erweiterte Daten

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
KlassePrenol lipids
SubclassTerpene lactones
Intermediate Tree Nodes Sesquiterpene lactones
Direct ParentGermacranolides and derivatives
Alternative Parents Germacrane sesquiterpenoids  Gamma butyrolactones  Tetrahydrofurans  Enoate esters  Oxacyclic compounds  Monocarboxylic acids and derivatives  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic heteropolycyclic compounds
Substituents Germacranolide - Germacrane sesquiterpenoid - Sesquiterpenoid - Gamma butyrolactone - Tetrahydrofuran - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Lactone - Carboxylic acid ester - Oxacycle - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organoheterocyclic compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Carbonyl group - Aliphatic heteropolycyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as germacranolides and derivatives. These are sesquiterpene lactones with a structure based on the germacranolide skeleton, characterized by a gamma lactone fused to a 1,7-dimethylcyclodec-1-ene moiety.
External Descriptors Germacrenes
3D-Struktur
Interaktives chemisches Strukturmodell





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PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)
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TERT Tchem Telomerase reverse transcriptase (2428 Activities)
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DU-145 (51482 Activities)
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RELA Tchem Nuclear factor NF-kappa-B p65 subunit (627 Activities)
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PA-1 (704 Activities)
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NLRP3 Tchem NACHT, LRR and PYD domains-containing protein 3 (908 Activities)
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Zugehörige Ziele (nicht menschlich)
murA UDP-N-acetylglucosamine 1-carboxyvinyltransferase (389 Activities)
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Hdac6 Histone deacetylase 6 (222 Activities)
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Enterococcus (1748 Activities)
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Staphylococcus aureus (210822 Activities)
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NIH3T3 (5395 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MYB Transcriptional activator Myb (118 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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.

6 results found

Lot NumberCertificate TypeDatumArtikel
G2608319G2608319Certificate of AnalysisJun 29, 2026 C139779
G2608320G2608320Certificate of AnalysisJun 29, 2026 C139779
G2608321G2608321Certificate of AnalysisJun 29, 2026 C139779
G2608322G2608322Certificate of AnalysisJun 29, 2026 C139779
C1908139C1908139Certificate of AnalysisApr 15, 2026 C139779
C1505108C1505108Certificate of AnalysisFeb 05, 2026 C139779
Chemische und physikalische Eigenschaften
LöslichkeitSoluble in ethanol (50 mM), DMSO (47 mg/ml at 25 °C), and water (<1 mg/ml at 25 °C).,
EmpfindlichkeitHeat Sensitive
Spezifische Drehung [α]118° (C=0.2,CHCl3)
Schmelzpunkt (°C)106°C(lit.)
Molekulargewicht232.320 g/mol
XLogP32.100
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Exact Mass232.146 Da
Monoisotopic Mass232.146 Da
Topological Polar Surface Area26.300 Ų
Heavy Atom Count17
Formal Charge0
Complexity401.000
Isotope Atom Count0
Defined Atom Stereocenter Count2
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count2
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds2
Covalently-Bonded Unit Count1
Citations of This Product
Lösungsrechner
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