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Molecule
ID:60162
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₂₀H₂₅NO₃
Molecular Mass
327.4174
Exact Mass
327.18344367
Charge
0
InChI
InChI=1S/C20H25NO3/c1-15(19(23)16-7-9-18(22)10-8-16)21-13-11-20(24,12-14-21)17-5-3-2-4-6-17/h2-10,15,19,22-24H,11-14H2,1H3/t15-,19+/m0/s1
InChIKey
QEMSVZNTSXPFJA-HNAYVOBHSA-N
Canonic Smiles
Oc1ccc(cc1)[C@@H]([C@@H](N1CCC(CC1)(O)c1ccccc1)C)O
Isomeric Smiles
c1c(ccc(c1)[C@@H]([C@H](C)N1CCC(CC1)(O)c1ccccc1)O)O
Calculated Properties
JChem
Acid pKa
9.540815
H Acceptors
4
H Donor
3
LogD (pH = 5.5)
-0.66286975
LogD (pH = 7.4)
1.0385036
Log P
2.0620441
Molar Refractivity
95.1894
Polarizability
37.28923
Polar Surface Area
63.93
Rotatable Bonds
4
Lipinski's Rule of Five
true
Data Source
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Registration numbers
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Properties
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Related Proteins
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
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IUPAC name
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MDL Number
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PubChem CID
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PubChem SID
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Molecular Spectra
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Sigma Aldrich
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
065361
Sigma Aldrich
SML0053
Academic Data
PubChem
219101
Names and Identifiers
IUPAC Traditional name
1-[(1S,2S)-1-hydroxy-1-(4-hydroxyphenyl)propan-2-yl]-4-phenylpiperidin-4-ol
traxoprodil
IUPAC name
1-[(1S,2S)-1-hydroxy-1-(4-hydroxyphenyl)propan-2-yl]-4-phenylpiperidin-4-ol
Synonyms
1-[(1S,2S)-2-Hydroxy-2-(4-hydroxyphenyl)-1-methylethyl]-4-phenylpiperidin-4-ol
CP-101,606
Traxoprodil; (1S,2S)-1-(4-hydroxy-phenyl)-2-(4-hydroxy-4-phenylpiperidino)-1-propanol; CP-101606
Registration numbers
CAS Number
134234-12-1
MDL Number
MFCD00926469
PubChem CID
219101
PubChem SID
162025903
Molecule Details
Sigma Aldrich
SML0053
Biochem/physiol Actions
Traxoprodil (CP-101,606) is a potent noncompetitive antagonist of N-methyl-D-aspartate (NMDA) receptors, selective for the NR2B subunit. It has been shown to be neuroprotective in animal models of brain injury and stroke.
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
MSDS Link
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Source
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Source
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
GHS Pictograms
Hazardous to the aquatic environment
Acute hazard, category1
Chronic hazard, categories 1,2
Source
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
Nature polluting (N)
Danger
Source
P273
-
P301+P310
-
P305+P351+P338
Source
H301
-
H319
-
H400
Source
25
-
36
-
50
Source
2-8°C
Source
26
-
45
-
61
Source
3
Source
Physical Property
white to tan powder
Source
DMSO: ≥35 mg/mL
Source
[α]/D +50 to +60° ( c=1, MeOH)
Source
Product Information
C20H25NO3
Source
≥98% (HPLC)
Source
Source
Source
Toxic (T)
Source
European Hazard Symbols
GHS Signal Word
GHS Precautionary statements
GHS Hazard statements
Risk Statements
Storage Temperature
Safety Statements
German water hazard class
Apperance
Solubility
Optical Rotation
Empirical Formula (Hill Notation)
Purity