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Thiorphan

HCID 3132
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Basic information

CAS
76721-89-6
Standard SMILES
O=C(O)CNC(=O)C(CS)Cc1ccccc1
InChIKey
LJJKNPQAGWVLDQ-UHFFFAOYSA-N
Molecular formula
C12H15NO3S
Average molar mass
253.32 g/mol
Monoisotopic mass
253.07726451

Overview

Thiorphan is a N-acyl-amino acid.

Names & identifiers

Preferred name
Thiorphan
IUPAC
2-[(2-benzyl-3-sulfanylpropanoyl)amino]acetic acid
English name
DL-THIORPHAN
Molecular formula
C12H15NO3S
Molecular weight
253.32

Names & synonyms

THIORPHANdl-thiorphan76721-89-6NSC-727676B79L7B5X3ZGlycine, N-(2-(mercaptomethyl)-1-oxo-3-phenylpropyl)-, (+-)-TiorphanXJ8Z52GK3X(3-Mercapto-2-benzylpropionyl)glycineRefChem:8979152-[(2-benzyl-3-sulfanylpropanoyl)amino]acetic acidRacecadotril EP impurity B
Show more names
C01619Thiorphan-d5THIORPHAN (DL)DL-THIORPHAN USP/EP/BPThiorphan, 10 mM in DMSOBisoprolol FuMarate IMpurity-Q(DL-3-MERCAPTO-2-BENZYLPROPANOYL)-GLY
2-(2-Benzyl-3-mercaptopropanamido)acetic acidMFCD00058435(+/-)-ThiorphanDL-3-Mercapto-2-benzylpropanoylglycineCHEMBL10247(DL-3-Mercapto-2-benzylpropanoyl)-Gly-OHN-[(RS)-2-Benzyl-3-mercaptopropanoyl]-glycine2-[(2-benzyl-3-sulfanyl-propanoyl)amino]acetic acid

Database identifiers

CAS
76721-89-6
PubChem CID
3132
DTXSID
DTXSID70868412
ChEMBL
CHEMBL10247
ChEBI
CHEBI:9568
UNII
B79L7B5X3Z
EC Number
881-424-0
Nikkaji
J531.930G

Properties

Computed structural properties

XLogP
1.3
Topological polar surface area
67.4 Ų
Hydrogen bond donors
3
Hydrogen bond acceptors
4
Rotatable bonds
6
Heavy atoms
17
Formal charge
0
Complexity
264

Physicochemical properties

Melting point
138 · 138-140 °C
Boiling point
524 · 524.0±50.0 °C(Predicted)
Density
1.246 · 1.246±0.06 g/cm3(Predicted)
RTECS
596440 · MC0596440
storage temp.
-15 °C · -15°C
solubility
50 mg/mL, · ethanol: 50 mg/mL, clear, colorless
form
White solid
pka
3.48 · 3.48±0.10(Predicted)
color
White to Off-White
BRN
4872101 · 4872101
InChI
1S/C12H15NO3S/c14-11(15)7-13-12(16)10(8-17)6-9-4-2-1-3-5-9/h1-5,10,17H,6-8H2,(H,13,16)(H,14,15)
InChIKey
LJJKNPQAGWVLDQ-UHFFFAOYSA-N
SMILES
OC(=O)CNC(=O)C(CS)Cc1ccccc1
CAS DataBase Reference
76721 · 76721-89-6
FDA UNII
79 L7B5X3Z · B79L7B5X3Z
UNSPSC Code
12352200 · 12352200

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

GHS classification

GHS ClassificationNot Classified

Hazard information

Hazard Classes and CategoriesNot Classified

Safety data

F
10
PPE
Eyeshields, Gloves, type N95 (US)
wgk
3
hs_code
29309090
Signal word
Warning
Symbol(GHS)
GHS07
safety_code
22-24/25
Storage Class
11 - Combustible Solids
Hazard statements
H302-H315-H319-H335
Precautionary statements
P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Chemistry & industry

Pharmacology

MeSH Pharmacological ClassificationCompounds which inhibit or antagonize biosynthesis or actions of proteases (ENDOPEPTIDASES).
Applications · 5 items

UsesAn Enkephalinase inhibitor

UsesThiorphan is a potent inhibitor of neprilysin, a membrane metallo-endopeptidase that cleaves peptide hormones, such as enkephalins, glucagon, and bradykinin (Ki = 4-140 nM). It is much less effective against neprilysin-2 (IC50 = 22.1 μM), angiotensin-converting enzyme, and endothelin-converting enzyme-1. Thiorphan can be produced in vivo via the metabolism of the prodrug acetorphan. Neprilysin is overexpressed in many forms of cancer and may play a role in protecting against Alzheimer’s disease.

UsesDL-Thiorphan has been used to evaluate the activity of NEP-dependent neutral endopeptidase. DL-Thiorphan has also been used for determining NEP enzymatic activity using fluorimetric assays.

UsesThe active metabolite

General DescriptionA thiol-containing amido-acid that selectively binds to the active site zinc of neprilysin (also known as neutral endopeptidase and NEP) and inhibits its activity (IC50 = 2.1 nM). Inhibits the β-amyloid (Aβ) degrading activity of neprilysin in vivo, but does not affect the secretion of either Aβ peptide or amyloid precursor protein (APP). Also shown to inhibit other neprilysin-related family members, such as mouse NL1 (IC50 = 47 nM) and the neprilysin homolog from Ascaris suum (IC50 = 22 μM). Inhibits the activity of angiotensin-converting enzyme (ACE) (IC50 = 140 nM), but has no effect on the activity of endothelin-converting enzyme (ECE).

Additional notes

DefinitionChEBI: Thiorphan is a N-acyl-amino acid.

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Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
NACRES
77 · NA.77
Symbol(GHS)
7 · GHS07
Signal word
Warning
Hazard statements
302 · H302-H315-H319-H335
Precautionary statements
261 · P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
PPE
95 · Eyeshields, Gloves, type N95 (US)
Safety Statements
22 · 22-24/25
WGK Germany
3 · 3
F
10 · 10
HS Code
29309090 · 29309090
Storage Class
11 · 11 - Combustible Solids