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M1699

Sigma-Aldrich

Montirelin trifluoroacetate salt

≥95% (HPLC)

Synonym(s):

(2R)-2-Mercaptopropanoyl-L-cysteinyl-L-histidyl-prolinamide, (3R,6R)-6-methyl-5-oxo-3-thiomorpholinecarbonyl-L-histidyl-L-Prolinamide, CG-3703, CNK-602A, NS-3, cyclic (1>2)-sulfide

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About This Item

Empirical Formula (Hill Notation):
C17H24N6O4S · xC2HF3O2
Molecular Weight:
408.48 (free base basis)
MDL number:
UNSPSC Code:
12352202
PubChem Substance ID:
NACRES:
NA.77

assay

≥95% (HPLC)

form

powder

color

white to off-white

solubility

H2O: ≥1 mg/mL

storage temp.

−20°C

SMILES string

OC(=O)C(F)(F)F.C[C@H]1SC[C@H](NC1=O)C(=O)N[C@H](CC(=O)N2CCC[C@H]2C(O)=O)Cc3c[nH]cn3

InChI

1S/C18H25N5O5S.C2HF3O2/c1-10-16(25)22-13(8-29-10)17(26)21-11(5-12-7-19-9-20-12)6-15(24)23-4-2-3-14(23)18(27)28;3-2(4,5)1(6)7/h7,9-11,13-14H,2-6,8H2,1H3,(H,19,20)(H,21,26)(H,22,25)(H,27,28);(H,6,7)/t10-,11+,13+,14+;/m1./s1

InChI key

YUARRBAFDZBNIK-JSQNCYBOSA-N

Biochem/physiol Actions

Montirelin is a potent, biologically stable TRH analog with Ki = 35.2 nM for brain receptor binding.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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