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22135-79-1 molecular structure
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(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-{[(1S,5R,13R,17S)-17-hydroxy-14-oxo-4-(prop-2-en-1-yl)-12-oxa-4-azapentacyclo[9.6.1.01,13.05,17.07,18]octadeca-7(18),8,10-trien-10-yl]oxy}oxane-2-carboxylic acid

ChemBase ID: 153201
Molecular Formular: C25H29NO10
Molecular Mass: 503.49846
Monoisotopic Mass: 503.17914613
SMILES and InChIs

SMILES:
C=CCN1CC[C@]23c4c5ccc(c4O[C@H]2C(=O)CC[C@]3([C@H]1C5)O)O[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)C(=O)O)O)O)O
Canonical SMILES:
C=CCN1CC[C@@]23[C@@]4([C@H]1Cc1c3c(O[C@H]2C(=O)CC4)c(cc1)O[C@@H]1O[C@H](C(=O)O)[C@H]([C@@H]([C@H]1O)O)O)O
InChI:
InChI=1S/C25H29NO10/c1-2-8-26-9-7-24-15-11-3-4-13(34-23-18(30)16(28)17(29)20(36-23)22(31)32)19(15)35-21(24)12(27)5-6-25(24,33)14(26)10-11/h2-4,14,16-18,20-21,23,28-30,33H,1,5-10H2,(H,31,32)/t14-,16+,17+,18-,20+,21+,23-,24+,25-/m1/s1
InChIKey:
DSRNCSJRHACUJL-JXOQMJNJSA-N

Cite this record

CBID:153201 http://www.chembase.cn/molecule-153201.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-{[(1S,5R,13R,17S)-17-hydroxy-14-oxo-4-(prop-2-en-1-yl)-12-oxa-4-azapentacyclo[9.6.1.01,13.05,17.07,18]octadeca-7(18),8,10-trien-10-yl]oxy}oxane-2-carboxylic acid
IUPAC Traditional name
(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-{[(1S,5R,13R,17S)-17-hydroxy-14-oxo-4-(prop-2-en-1-yl)-12-oxa-4-azapentacyclo[9.6.1.01,13.05,17.07,18]octadeca-7(18),8,10-trien-10-yl]oxy}oxane-2-carboxylic acid
Synonyms
(5α)-4,5-Epoxy-14-hydroxy-6-oxo-17-(2-propenyl)morphinan-3-yl β-D-Glucopyranosiduronic Acid
Naloxone-3-glucuronide
Naloxone 3-β-D-Glucuronide, > 90%
Naloxone-3-glucuronide
CAS Number
22135-79-1
MDL Number
MFCD00878774
PubChem SID
162247340
PubChem CID
71311610

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
PubChem 71311610 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 2.6801634  H Acceptors 11 
H Donor LogD (pH = 5.5) -3.0590346 
LogD (pH = 7.4) -3.172641  Log P -3.0590029 
Molar Refractivity 120.734 cm3 Polarizability 48.204147 Å3
Polar Surface Area 166.22 Å2 Rotatable Bonds
Lipinski's Rule of Five false 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Apperance
white expand Show data source
White to Off-White Solid expand Show data source
Melting Point
200-205 °C expand Show data source
214-216°C expand Show data source
Storage Condition
-20°C Freezer expand Show data source
MSDS Link
Download expand Show data source
Download expand Show data source
German water hazard class
3 expand Show data source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand Show data source
Drug Control
regulated under CDSA - not available from Sigma-Aldrich Canada expand Show data source
Storage Temperature
2-8°C expand Show data source
Certificate of Analysis
Download expand Show data source
Empirical Formula (Hill Notation)
C25H29NO10 expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich TRC TRC
Sigma Aldrich - UC322 external link
Biochem/physiol Actions
Phase II metabolite of naloxone.
Toronto Research Chemicals - N285010 external link
A metabolite of Naloxone. Narcotic antagonist.

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • • Scheurer, U., et al.: J. Pharmacol. Exp. Ther., 252, 1324 (1990)
  • • Yuan, C., et al.: Clin. Pharmacol. Ther., 59, 469 (1990)
  • • Ulens, C., et al.: Biochem. Pharmacol., 62, 1273 (1990)
  • • Comert, M., et al.: Eur. J. Pharmacol., 511, 183 (1990)
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PATENTS

PATENTS

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INTERNET

INTERNET

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