ChemicalBook--->CAS DataBase List--->38101-59-6

38101-59-6

38101-59-6 Structure

38101-59-6 Structure
IdentificationBack Directory
[Name]

H-GLU-TRP-OH
[CAS]

38101-59-6
[Synonyms]

EW
Timogen
GLU-TRP
Z-Glu-Trp
Ccris 8677
NSC 334073
Oglufanide
Glu-Trp HAc
H-GLU-TRP-OH
ALPHA-L-GLU-L-TRP
Glutamyltryptophan
Glutamyl tryptophan
Thymogen(Oglufanide)
L-Glutamyl-L-tryptophan
alpha-glutamyltryptophan
L-Tryptophan, L-α-glutamyl-
ThyMogen, Oglufanide, IM862
L-Tryptophan, L-a-glutaMyl-
L-alpha-Glutamyl-L-tryptophan
L-Tryptophan, N-L-alpha-glutamyl-
H-GLU-TRP-OH;L-GLUTAMYL-L-TRYPTOPHAN;THYMOGEN;IM862
4-amino-5-[[1-carboxy-2-(1H-indol-3-yl)ethyl]amino]-5-oxopentanoicacid
[Molecular Formula]

C16H19N3O5
[MDL Number]

MFCD00037953
[MOL File]

38101-59-6.mol
[Molecular Weight]

333.34
Chemical PropertiesBack Directory
[Melting point ]

121-122℃
[Boiling point ]

738.9±60.0 °C(Predicted)
[density ]

1.428
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[solubility ]

DMSO : 15.5 mg/mL (46.50 mM)
[form ]

Solid
[pka]

3.09±0.10(Predicted)
[color ]

White to off-white
[InChI]

InChI=1/C16H19N3O5/c17-11(5-6-14(20)21)15(22)19-13(16(23)24)7-9-8-18-12-4-2-1-3-10(9)12/h1-4,8,11,13,18H,5-7,17H2,(H,19,22)(H,20,21)(H,23,24)/t11-,13-/s3
[InChIKey]

LLEUXCDZPQOJMY-PZILLZCRNA-N
[SMILES]

C(C1=CNC2=CC=CC=C12)[C@@H](C(=O)O)NC(=O)[C@@H](N)CCC(=O)O |&1:10,17,r|
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictogramsGHS hazard pictograms
GHS07,GHS02
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H226
[Precautionary statements ]

P501-P240-P210-P233-P243-P241-P242-P264-P280-P370+P378-P337+P313-P305+P351+P338-P362+P364-P303+P361+P353-P332+P313-P403+P235
Hazard InformationBack Directory
[Uses]

Treatment of Kaposi’s sarcoma and solid tumor cancers (angiogenesis inhibitor); immunomodulator.
[Definition]

ChEBI: A dipeptide composed of L-glutamic acid and L-tryptophan joined by a peptide linkage.
[in vivo]

Oglufanide (L-glu-L-trp) (1-100 mg/kg/day; s.c.; 10 days) has antitumor activity in immunocompetent and immunodeficient mice[4].

Animal Model:C57BL/6 immune competent mice, Lewis lung carcinoma (LLC) xenograft; Balb/C athymic mice, M21 human melanoma xenograft[4]
Dosage:1, 10, 50 and 100 mg/kg/day
Administration:Subcutaneous injection, 10 days
Result:Resulted in a dose-dependent inhibition of LLC tumor growth in syngeneic immune competent mice and showed a dose-dependent decrease in tumor volumes of xenografts in Balb/C athymic mice implanted with M21 human melanoma cells.
[IC 50]

VEGFR; HCV; Human Endogenous Metabolite
Spectrum DetailBack Directory
[Spectrum Detail]

H-GLU-TRP-OH(38101-59-6)1HNMR
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