ChemicalBook--->CAS DataBase List--->228266-40-8

228266-40-8

228266-40-8 Structure

228266-40-8 Structure
IdentificationBack Directory
[Name]

TANDUTINIB
[CAS]

228266-40-8
[Synonyms]

CS-1371
Hti 286
Spa 110
Taltobulin
Unii-J6D6912bxs
HTI-286;SPA-110
Taltobulin (HTI-286)
HTI-286 hydrochloride
SPA-110 hydrochloride
HTI-286 HYDROCHLORIDE;SPA-110 HYDROCHLORIDE
N,β,β-Trimethyl-L-phenylalanyl-N-[(3S,4E)-5-carboxy-2-methyl-4-hexen-3-yl]-N,3-dimethyl-L-valinamide
L-Valinamide, N,β,β-trimethyl-L-phenylalanyl-N-[(1S,2E)-3-carboxy-1-(1-methylethyl)-2-buten-1-yl]-N,3-dimethyl-
N,beta,beta-Trimethyl-L-phenylalanyl-N-[(1S,2E)-3-carboxy-1-(1-methylethyl)-2-butenyl]-N,3-dimethyl-L-valinamide
L-Valinamide, N,beta,beta-trimethyl-L-phenylalanyl-N-((1S,2E)-3-carboxy-1-(1-methylethyl)-2-butenyl)-N,3-dimethyl-
[Molecular Formula]

C27H43N3O4
[MDL Number]

MFCD07772353
[MOL File]

228266-40-8.mol
[Molecular Weight]

473.66
Chemical PropertiesBack Directory
[Melting point ]

135-137 ºC
[Boiling point ]

662.4±55.0 °C(Predicted)
[density ]

1.063
[storage temp. ]

Sealed in dry,Store in freezer, under -20°C
[solubility ]

DMSO: 40 mg/ml
[form ]

A solid
[pka]

4.68±0.19(Predicted)
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
Hazard InformationBack Directory
[Uses]

Treatment of solid tumors.
[in vivo]

Taltobulin (HTI-286; 1.6 mg/kg i.v.) inhibits the growth of human tumor xenografts (e.g., HCT-15, DLD-1, MX-1W, and KB-8-5) in athymic nu/nu female mice[1].
? Taltobulin (HTI-286; 3 mg/kg; p.o. gavage) inhibits growth by 97.3 % and 82% in athymic nu/nu female mice with Lox melanoma xenografts and KB-3-1 epidermoid xenograft model, respectively[1].

Animal Model:Athymic nu/nu female mice with Lox melanoma model (5-6 weeks of age)[1]
Dosage:1.6 mg/kg
Administration:Administered i.v.;for 35 days
Result:Growth of Lox tumors was inhibited by 96-98% on day 12 compared with vehicle-treated controls.
Growth of KB-8-5 tumors was inhibited by 84% on day 14 compared with vehicle-treated controls.
Growth of MX-1W tumors was inhibited by 97% compared with vehicle-treated controls.
Growth of DLD-1 and HCT-15 tumors was inhibited by 80 and 66%, respectively.
[IC 50]

Traditional Cytotoxic Agents
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