INNO-206 - ≥98% , DNA topoisomerase II alpha inhibitor, CAS No.1361644-26-9, DNA topoisomerase II alpha inhibitor

CAS: 1361644-26-9 Cat. No.: I125675 Formula: C37H42N4O13 Peso molecolare: 750.75 Numero EC: 813-952-4
Disponibile su ordine
GRADE & PURITY ≥98%
Synonyms
AKOS030526452 | 1H-PYRROLE-1-HEXANOIC ACID, 2,5-DIHYDRO-2,5-DIOXO-, (1-(4-((3-AMINO-2,3,6-TRIDEOXY-.ALPHA.-L-LYXO-HEXOPYRANOSYL)OXY)-1,2,3,4,6,11-HEXAHYDRO-2,5,12-TRIHYDROXY-7-METHOXY-6,11-DIOXO-2-NAPHTHACENYL)-2-HYDROXYETHYLIDENE)HYDRAZIDE, (2S-CIS)- | M
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
★
Size
Germania (EU)
USA*
Price
Qty
10mg
I125675-10mg
Su ordinazione · 8–12 settimane

236,81€

355,69€
Salva 118,88 € (33.42%)
20mg
I125675-20mg
Su ordinazione · 8–12 settimane

425,97€

639,44€
Salva 213,46 € (33.38%)
50mg
I125675-50mg
Su ordinazione · 8–12 settimane

931,00€

1.396,97€
Salva 465,98 € (33.36%)
100mg
I125675-100mg
Su ordinazione · 8–12 settimane

1.674,65€

2.512,02€
Salva 837,37 € (33.33%)
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

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.

Specifications

Sinonimi
AKOS030526452 | 1H-PYRROLE-1-HEXANOIC ACID, 2,5-DIHYDRO-2,5-DIOXO-, (1-(4-((3-AMINO-2,3,6-TRIDEOXY-.ALPHA.-L-LYXO-HEXOPYRANOSYL)OXY)-1,2,3,4,6,11-HEXAHYDRO-2,5,12-TRIHYDROXY-7-METHOXY-6,11-DIOXO-2-NAPHTHACENYL)-2-HYDROXYETHYLIDENE)HYDRAZIDE, (2S-CIS)- | M
Specifiche e purezza
≥98%
Meccanismi biochimici e fisiologici

INNO-206 (Aldoxorubicin) is the 6-maleimidocaproyl hydrazone derivative prodrug of the anthracycline antibiotic doxorubicin (DOXO-EMCH) with antineoplastic activity. Following intravenous administration, doxorubicin prodrug INNO-206 binds

Condizioni di conservazione di stoccaggio
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.
Tipo di azione
INHIBITOR
Meccanismo d'azione
DNA topoisomerase II alpha inhibitor
Purezza
≥98%
Proprietà del prodotto
ALogP1.3
Nomi e identificatori
Sorrisi canoniciCC1C(C(CC(O1)OC2CC(CC3=C2C(=C4C(=C3O)C(=O)C5=C(C4=O)C(=CC=C5)OC)O)(C(=NNC(=O)CCCCCN6C(=O)C=CC6=O)CO)O)N)O
IUPAC NameN-[(E)-[1-[(2S,4S)-4-[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-methyloxan-2-yl]oxy-2,5,12-trihydroxy-7-methoxy-6,11-dioxo-3,4-dihydro-1H-tetracen-2-yl]-2-hydroxyethylidene]amino]-6-(2,5-dioxopyrrol-1-yl)hexanamide
InChIKeyOBMJQRLIQQTJLR-USGQOSEYSA-N
INCHI1S/C37H42N4O13/c1-17-32(46)20(38)13-27(53-17)54-22-15-37(51,23(16-42)39-40-24(43)9-4-3-5-12-41-25(44)10-11-26(41)45)14-19-29(22)36(50)31-30(34(19)48)33(47)18-7-6-8-21(52-2)28(18)35(31)49/h6-8,10-11,17,20,22,27,32,42,46,48,50-51H,3-5,9,12-16,38H2,1-2H3,(H,40,43)/b39-23+/t17-,20-,22-,27-,32+,37-/m0/s1
Isomeri SMILES C[C@H]1[C@H]([C@H](C[C@@H](O1)O[C@H]2C[C@@](CC3=C2C(=C4C(=C3O)C(=O)C5=C(C4=O)C(=CC=C5)OC)O)(/C(=N/NC(=O)CCCCCN6C(=O)C=CC6=O)/CO)O)N)O
Peso molecolare 750.75
Reaxy-Rn 61753403
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=61753403&ln=

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
SuperclassPhenylpropanoids and polyketides
ClasseAnthracyclines
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentAnthracyclines
Alternative Parents Tetracenequinones  Aminoglycosides  Anthraquinones  Hexoses  O-glycosyl compounds  Tetralins  Aryl ketones  Anisoles  Maleimides  Alkyl aryl ethers  N-substituted carboxylic acid imides  Oxanes  Dicarboximides  Vinylogous acids  Tertiary alcohols  Pyrrolines  Secondary alcohols  1,2-aminoalcohols  Amino acids and derivatives  Acetals  Polyols  Oxacyclic compounds  Azacyclic compounds  Organopnictogen compounds  Aldehydes  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Primary alcohols  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Anthracycline - Anthracyclinone-skeleton - Aminoglycoside core - Tetracenequinone - 9,10-anthraquinone - 1,4-anthraquinone - Anthracene - Hexose monosaccharide - Glycosyl compound - O-glycosyl compound - Tetralin - Aryl ketone - Anisole - Amino saccharide - Maleimide - Alkyl aryl ether - Monosaccharide - Carboxylic acid imide, n-substituted - Oxane - Benzenoid - Dicarboximide - Tertiary alcohol - Vinylogous acid - Carboxylic acid imide - Pyrroline - Ketone - Secondary alcohol - 1,2-aminoalcohol - Amino acid or derivatives - Acetal - Polyol - Oxacycle - Carboxylic acid derivative - Ether - Azacycle - Organoheterocyclic compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organic nitrogen compound - Carbonyl group - Aldehyde - Organonitrogen compound - Primary aliphatic amine - Primary alcohol - Amine - Primary amine - Aromatic heteropolycyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as anthracyclines. These are polyketides containing a tetracenequinone ring structure with a sugar attached by glycosidic linkage.
External Descriptors Not available
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (non umani)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
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:
Proprietà chimiche e fisiche
SolubilitàDMSO
Peso molecolare750.700 g/mol
XLogP31.300
Hydrogen Bond Donor Count7
Hydrogen Bond Acceptor Count15
Rotatable Bond Count12
Exact Mass750.275 Da
Monoisotopic Mass750.275 Da
Topological Polar Surface Area268.000 Ų
Heavy Atom Count54
Formal Charge0
Complexity1510.000
Isotope Atom Count0
Defined Atom Stereocenter Count6
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds1
Covalently-Bonded Unit Count1
Domande frequenti e articoli
Calcolatori di soluzioni
Recensioni

Recensioni dei clienti

Domande frequenti

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 1361644-26-9, the molecular formula is C37H42N4O13, and the molecular weight is 750.75 g/mol. InChIKey OBMJQRLIQQTJLR-USGQOSEYSA-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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