ChemicalBook--->CAS DataBase List--->181816-48-8

181816-48-8

181816-48-8 Structure

181816-48-8 Structure
IdentificationBack Directory
[Name]

Ombrabulin
[CAS]

181816-48-8
[Synonyms]

CS-1038
AVE-8062
Ombrabuli
ombrabulin
RPR-258062A.
CS-39-L-Ser.HCl
OMbrabulin(AVE-8062)
AVE8062;AC-7700;CS-39-L-SER.HCL;AVE-8062A;AVE-8062;RPR-258062A.
(S,Z)-2-Amino-3-hydroxy-N-(2-methoxy-5-(3,4,5-trimethoxystyryl)phenyl)propanamide
AVE8062; AVE8062A; AC7700; AVE-8062; AVE-8062A; AC-7700; AVE 8062; AVE 8062A; AC 7700
(2S)-2-amino-3-hydroxy-N-[2-methoxy-5-[(Z)-2-(3,4,5-trimethoxyphenyl)ethenyl]phenyl]propanamide
(2S)-2-Amino-3-hydroxy-N-[2-methoxy-5-[(1Z)-2-(3,4,5-trimethoxyphenyl)ethenyl]phenyl]propanamide
PropanaMide,2-aMino-3-hydroxy-N-[2-Methoxy-5-[(1Z)-2-(3,4,5-triMethoxyphenyl)ethenyl]phenyl]-,(2S)-
[Molecular Formula]

C21H26N2O6
[MDL Number]

MFCD00951209
[MOL File]

181816-48-8.mol
[Molecular Weight]

402.44
Chemical PropertiesBack Directory
[Boiling point ]

648.1±55.0 °C(Predicted)
[density ]

1.258
[storage temp. ]

Sealed in dry,2-8°C
[solubility ]

Soluble in DMSO
[form ]

Oil
[pka]

12.03±0.10(Predicted)
[color ]

Colorless to light yellow
Hazard InformationBack Directory
[Uses]

Ombrabulin is a vascular disrupting agent that enhances the standard therapies in head and neck squamous cell carcinomas.
[in vivo]

Before performing therapy experiments, the tolerability of various doses of Ombrabulin (AC-7700) ranging from 10 to 100 mg/kg is tested given twice weekly via i.v., i.p., or s.c. routes in nude mice (n=3 per group). The i.v. and s.c. routes are not pursued further due to problems with skin or tail vein necrosis. The i.p. route is well tolerated with doses up to 100 mg/kg. Next, preliminary experiments are done to determine the lowest dose for in vivo therapeutic efficacy. Starting 7 days after tumor cell injection, nude mice (n=5 per group) bearing HeyA8 ovarian cancer cells are treated with either vehicle or Ombrabulin 10, 30, 50, and 100 mg/kg twice weekly i.p. for 3 weeks. There is 65% reduction in tumor weight in the 30 mg/kg group compared with the vehicle control group (P<0.02). The 10 mg/kg dose is not effective. The antitumor effects at doses >30 mg/kg are not significantly better; therefore, the 30 mg/kg dose is selected for subsequent therapy experiments[1].

[storage]

Store at -20°C
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