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ChemicalBook--->CAS DataBase List--->91421-42-0

91421-42-0

91421-42-0 Structure

91421-42-0 Structure
IdentificationMore
[Name]

Rubitecan
[CAS]

91421-42-0
[Synonyms]

(4s)-4-ethyl-4-hydroxy-10-nitro-1h-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4h,12h)-dione
9-NITRO-20(S)-CAMPTOTHECIN
9-NITROCAMPTOTHECIN
9-NITRO-CPT
CAMPTOTHECIN, 9-NITRO-20(S)-
orathecin
RUBETICAN
RUBITECAN
Rubitecane
(4S)-4-Ethyl-4-hydroxy-10-nitro-1H-pyrano[346,7]indolizinol[1,2-b]quinoline-3, 14(4H,-12H)-dione
9-NC
Oratheci
9-Nitrocamptothecin
[Molecular Formula]

C20H15N3O6
[MDL Number]

MFCD06656294
[Molecular Weight]

393.35
[MOL File]

91421-42-0.mol
Chemical PropertiesBack Directory
[Appearance]

Yellow Amorphous Powder
[Melting point ]

182-186°C
[alpha ]

D23 +27° (c = 0.2 in CH3OH-CHCl3, 1:4)
[Boiling point ]

816.3±65.0 °C(Predicted)
[density ]

1.63
[Fp ]

106℃
[storage temp. ]

Room temp
[solubility ]

DMSO, Chloroform, Methanol
[form ]

Solid
[pka]

11.16±0.20(Predicted)
[color ]

Yellow
[Usage]

Semisynthetic camptothecin which inhibits DNA topoisomerase I. Prodrug of 9-aminocamptothecin. Antineoplastic
[Merck ]

14,8288
[CAS DataBase Reference]

91421-42-0(CAS DataBase Reference)
Safety DataBack Directory
[Safety Statements ]

24/25
[WGK Germany ]

3
[RTECS ]

UQ0493300
[HS Code ]

29399990
Questions And AnswerBack Directory
[Description]

Rubitecan, marketed by Supergen as Orathecin, is a promising oral treatment for solid melanoma, prostate, breast, ovarian, and other cancers, as well as leukemia. It is a derivative of camptothecin, a topoisomerase inhibitor known from Chinese Traditional Medicine. It selectively targets the critical S-stage of cellular reproduction – particularly in acidic environments, as in many cancer cells – relaxing DNA supercoiling and generating lethal breaks in the DNA. Due to insolubility, its biological delivery mechanism is not yet effective, and it has not been approved for clinical use.
[Reference]

https://www.sciencedirect.com/topics/medicine-and-dentistry/rubitecan
https://en.wikipedia.org/wiki/Rubitecan
https://en.wikipedia.org/wiki/Topoisomerase_inhibitor
https://en.wikipedia.org/wiki/Camptothecin#cite_note-Y.Pommier_2003-14
https://www.ncbi.nlm.nih.gov/pubmed/1995300
Hazard InformationBack Directory
[Chemical Properties]

Yellow Amorphous Powder
[Uses]

Semisynthetic camptothecin which inhibits DNA topoisomerase I. Prodrug of 9-aminocamptothecin. Antineoplastic
[Definition]

ChEBI: A pyranoindolizinoquinoline that is camptothecin in which the hydrogen at position 9 has been replaced by a nitro group. It is a prodrug for 9-aminocamptothecin.
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

91421-42-0(sigmaaldrich)
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