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Chemical structure of Neuropeptide GE

GA23252

Neuropeptide GE

Also known as (2S)-2-[[(2S)-5-amino-2-[[(2S,3R)-2-[[(2S)-2-[[(2S)-2-[[(2S,3R)-2-[[(2S)-4-amino-2-[[(2S)-5-amino-2-[[(2S)-2-[[2-[[(2S)-4-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-1-[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[(2-aminoacetyl)amino]-3-hydroxypropanoyl]amino]-3-methylbutanoyl]amino]propanoyl]amino]-3-phenylpropanoyl]pyrrolidine-2-carbonyl]amino]propanoyl]amino]-4-carboxybutanoyl]amino]-4-oxobutanoyl]amino]acetyl]amino]-3-methylbutanoyl]amino]-5-oxopentanoyl]amino]-4-oxobutanoyl]amino]-3-hydroxybutanoyl]amino]-4-carboxybutanoyl]amino]-3-hydroxypropanoyl]amino]-3-hydroxybutanoyl]amino]-5-oxopentanoyl]amino]pentanedioic acid

A peptide derived by proteolytic cleavage from the rat melanin-concentrating hormone (MCH) precursor· Neuropeptide glycine-glutamic acid (NGE) was suggested to act as a neuroregulator

ChemicalCAS134748-04-2MW1965.02FormulaC81H125N23O34
CAS number
134748-04-2
Molecular weight
1965.02
Formula
C81H125N23O34
Solubility
Soluble in DMSO
InChIKey
KZNJHPULEYPZBD-LMXVNMMBSA-N
Catalogue number
GA23252
Brand
GLPBIO
Computed properties PubChem CID 16180048 · XLogP -14.8 · TPSA 944 Ų · H-bond donors 30
XLogP
-14.8
TPSA
944 Ų
H-bond donors
30
H-bond acceptors
35
Rotatable bonds
63
Heavy atoms
138

SMILES C[C@H]([C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCC(=O)N)C(=O)N[C@@H](CCC(=O)O)C(=O)O)NC(=O)[C@H](CC(=O)N)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](C(C)C)NC(=O)CNC(=O)[C@H](CC(=O)N)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC2=CC=CC=C2)NC(=O)[C@H](C)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CO)NC(=O)CN)O

Computed descriptors from PubChem (CID 16180048), public domain. Identity cross-checked against the supplier's molecular formula and weight — verify before use.

Ordering in Israel

Lead time
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