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Valrubicin , DNA inhibitor, CAS No.56124-62-0, DNA inhibitor

Item Number
V335774
Grouped product items
SKUSizeAvailabilityPrice Qty
V335774-1mg
1mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$59.90
V335774-5mg
5mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$149.90
V335774-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$219.90
V335774-25mg
25mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$369.90
V335774-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$539.90
V335774-100mg
100mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$749.90

a chemotherapy drug used to treat cancer

Basic Description

SynonymsValrubicin|56124-62-0|Valstar|AD-32|Antibiotic AD 32|Valstar Preservative Free|AD 32|NSC-246131|UNII-2C6NUM6878|N-Trifluoroacetyldoxorubicin 14-valerate|DTXSID9046497|HSDB 7288|2C6NUM6878|Valrubicin (AD-32)|N-Trifluoroacetyladriamycin-14-valerate|NSC 2461
Biochemical and Physiological MechanismsValrubicin is a semisynthetic derivative of the antineoplastic anthracycline antibiotic doxorubicin. Valrubicin is converted intracytoplasmically into N-trifluoroacetyladriamycin, which interacts with topoisomerase II, stabilizing the complex between the
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
Action TypeINHIBITOR
Mechanism of actionDNA inhibitor
Product Description

Valrubicin is a chemotherapy drug used to treat cancer of the bladder.

Product Properties

ALogP4

Associated Targets

HDAC6 Tclin Histone deacetylase 6 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ABCC2 Tchem Canalicular multispecific organic anion transporter 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ABCC3 Tbio Canalicular multispecific organic anion transporter 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ABCC4 Tchem Multidrug resistance-associated protein 4 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ABCB11 Tchem Bile salt export pump 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name [2-oxo-2-[(2S,4S)-2,5,12-trihydroxy-4-[(2R,4S,5S,6S)-5-hydroxy-6-methyl-4-[(2,2,2-trifluoroacetyl)amino]oxan-2-yl]oxy-7-methoxy-6,11-dioxo-3,4-dihydro-1H-tetracen-2-yl]ethyl] pentanoate
INCHI InChI=1S/C34H36F3NO13/c1-4-5-9-21(40)49-13-20(39)33(47)11-16-24(19(12-33)51-22-10-17(27(41)14(2)50-22)38-32(46)34(35,36)37)31(45)26-25(29(16)43)28(42)15-7-6-8-18(48-3)23(15)30(26)44/h6-8,14,17,19,22,27,41,43,45,47H,4-5,9-13H2,1-3H3,(H,38,46)/t14-,17-,19-,22-,27+,33-/m0/s1
InChi Key ZOCKGBMQLCSHFP-KQRAQHLDSA-N
Canonical SMILES CCCCC(=O)OCC(=O)C1(CC(C2=C(C1)C(=C3C(=C2O)C(=O)C4=C(C3=O)C=CC=C4OC)O)OC5CC(C(C(O5)C)O)NC(=O)C(F)(F)F)O
Isomeric SMILES CCCCC(=O)OCC(=O)[C@]1(C[C@@H](C2=C(C1)C(=C3C(=C2O)C(=O)C4=C(C3=O)C=CC=C4OC)O)O[C@H]5C[C@@H]([C@@H]([C@@H](O5)C)O)NC(=O)C(F)(F)F)O
PubChem CID 454216
Molecular Weight 723.64

Certificates

Certificate of Analysis(COA)

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12 results found

Lot NumberCertificate TypeDateItem
D2419171Certificate of AnalysisFeb 04, 2024 V335774
D2419172Certificate of AnalysisFeb 04, 2024 V335774
D2419247Certificate of AnalysisFeb 04, 2024 V335774
D2419248Certificate of AnalysisFeb 04, 2024 V335774
D2419249Certificate of AnalysisFeb 04, 2024 V335774
D2419250Certificate of AnalysisFeb 04, 2024 V335774
D2419251Certificate of AnalysisFeb 04, 2024 V335774
D2419252Certificate of AnalysisFeb 04, 2024 V335774
D2419254Certificate of AnalysisFeb 04, 2024 V335774
D2419255Certificate of AnalysisFeb 04, 2024 V335774
D2419387Certificate of AnalysisFeb 04, 2024 V335774
D2419388Certificate of AnalysisFeb 04, 2024 V335774

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Chemical and Physical Properties

SolubilitySoluble in DMSO, and methanol.
Melt Point(°C)202-205° C

Safety and Hazards(GHS)

Pictogram(s) GHS06,   GHS08,   GHS07
Signal Danger
Hazard Statements

H301:Toxic if swallowed

H351:Suspected of causing cancer

H312:Harmful in contact with skin

H332:Harmful if inhaled

H360:May damage fertility or the unborn child

H340:May cause genetic defects

H350:May cause cancer

H361:Suspected of damaging fertility or the unborn child

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352:IF ON SKIN: wash with plenty of water.

P321:Specific treatment (see ... on this label).

P405:Store locked up.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P281:Use personal protective equipment as required.

P271:Use only outdoors or in a well-ventilated area.

P270:Do not eat, drink or smoke when using this product.

P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing.

P362+P364:Take off contaminated clothing and wash it before reuse.

P330:Rinse mouth.

P203:Obtain, read and follow all safety instructions before use.

P301+P316:IF SWALLOWED: Get emergency medical help immediately.

P318:if exposed or concerned, get medical advice.

P317:Get emergency medical help.

Related Documents

Solution Calculators