STRUCTURE VIEWER

The molecule behind every compound

Structure figures drawn from the sequence on the record, with the molecular formula, mass, CAS number and residue-level composition for each compound in the catalog. Figures show connectivity, not a measured conformation; identity for a given lot is reported on its lab report.

10 COMPOUNDS IN THE CATALOG

C10H17N3O6SMW 307.33 DaCAS 70-18-8

Skeletal formula · hand-built from the structure record

SHORT PEPTIDES

L-Glutathione

Tripeptide · γ-Glu-Cys-Gly

FORMULA: C10H17N3O6S
MOL. WEIGHT: 307.33 Da
CAS: 70-18-8
RESIDUES: 3

PRIMARY SEQUENCE · N → C TERMINUS3 RESIDUES

EGlu
CCys
GGly

Hydrophobic
Polar
Basic (+)
Acidic (−)
Gly / Pro
Modified / non-standard

COMPOSITION

Cys1
Glu1
Gly1

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The reduced tripeptide thiol. The glutamate is joined to cysteine through its side-chain (gamma) carboxyl, not the alpha carboxyl, which is why it is drawn off the main chain.

Formula, mass and CAS from the PubChem glutathione record. PubChem CID 124886

Skeletal formulae are generated from the sequence on record and show connectivity, not a measured 3D conformation. Peptides longer than 16 residues are shown as a residue chain. Formula and mass are nominal values for the parent compound; identity for a given lot is reported on its lab report. House designations are drawn only as a residue count with unspecified positions, and blends are never drawn as a single molecule. A reference diagram is not evidence of batch identity, purity, or suitability for any use.