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50847-11-5 molecular structure
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2-methyl-1-[2-(propan-2-yl)pyrazolo[1,5-a]pyridin-3-yl]propan-1-one

ChemBase ID: 4411
Molecular Formular: C14H18N2O
Molecular Mass: 230.30552
Monoisotopic Mass: 230.14191321
SMILES and InChIs

SMILES:
O=C(c1c(nn2c1cccc2)C(C)C)C(C)C
Canonical SMILES:
CC(C(=O)c1c(nn2c1cccc2)C(C)C)C
InChI:
InChI=1S/C14H18N2O/c1-9(2)13-12(14(17)10(3)4)11-7-5-6-8-16(11)15-13/h5-10H,1-4H3
InChIKey:
ZJVFLBOZORBYFE-UHFFFAOYSA-N

Cite this record

CBID:4411 http://www.chembase.cn/molecule-4411.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
2-methyl-1-[2-(propan-2-yl)pyrazolo[1,5-a]pyridin-3-yl]propan-1-one
IUPAC Traditional name
ketas
ibudilast
2-methyl-1-[2-(propan-2-yl)pyrazolo[1,5-a]pyridin-3-yl]propan-1-one
Synonyms
MN-166
AV-411
2-Isopropyl-3-isobutyrylpyrazolo(1,5-a)pyridine
3-Isobutyryl-2-isopropylpyrazolo[1,5-a]pyridine
3-isobutyryl-2-isopropylpyrazolo(1,5-a)pyridine
Eyevinal
I0157_SIGMA
Ibudilast (jan/inn)
Ibudilast [inn:jan]
Ibudilastum
Ibudilastum [latin]
Ke tas
Ketas
Ketas (TN)
Lopac-I-0157
Pyrazolo(1,5-a)pyridine, 3-isobutyryl-2-isopropyl-
Tocris-1694
UNII-M0TTH61XC5
Ibudilast
2-Methyl-1-[2-(1-methylethyl)pyrazolo[1,5-a]pyridin-3-yl] 1-propanone
KC-404
Ibudilast
2-Methyl-1-[2-(1-methylethyl)pyrazolo[1,5-a]pyridin-3-yl]-1-propanone
1-(2-Isopropylpyrazolo[1,5-a]pyridin-3-yl)-2-methylpropan-1-one
2-Isopropyl-3-isobutyrylpyrazolo[1,5-a]pyridine
AV 411
KC 404
CAS Number
50847-11-5
MDL Number
MFCD00864808
PubChem SID
160967843
99443231
24278482
PubChem CID
3671

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem ALOGPS 2.1
Acid pKa 16.124111  H Acceptors
H Donor LogD (pH = 5.5) 3.6791465 
LogD (pH = 7.4) 3.6792438  Log P 3.679245 
Molar Refractivity 79.375 cm3 Polarizability 26.83163 Å3
Polar Surface Area 34.37 Å2 Rotatable Bonds
Lipinski's Rule of Five true 
Log P 3.36  LOG S -3.11 
Solubility (Water) 1.79e-01 g/l 

PROPERTIES

PROPERTIES

Physical Property Safety Information Pharmacology Properties Product Information Bioassay(PubChem)
Solubility
Chloroform expand Show data source
Dichloromethane expand Show data source
DMSO: soluble28 mg/mL expand Show data source
Ether expand Show data source
H2O: soluble4.5 mg/mL expand Show data source
Hexane, expand Show data source
Apperance
white solid expand Show data source
White Solid expand Show data source
Melting Point
43-46°C expand Show data source
Storage Condition
-20°C Freezer expand Show data source
RTECS
UR0711200 expand Show data source
European Hazard Symbols
Harmful Harmful (Xn) 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
Risk Statements
22-36/37/38 expand Show data source
Safety Statements
26-36 expand Show data source
GHS Pictograms
GHS07 expand Show data source
GHS Signal Word
Warning expand Show data source
GHS Hazard statements
H302-H315-H319-H335 expand Show data source
GHS Precautionary statements
P261-P305 + P351 + P338 expand Show data source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves expand Show data source
Storage Temperature
2-8°C expand Show data source
Gene Information
human ... PDE4A(5141), PDE4B(5142), PDE4C(5143), PDE4D(5144) expand Show data source
Mechanism of Action
Bronchodilator expand Show data source
Lowers Ca 2+ deposition in soft tissues expand Show data source
Phosphodiesterase inhibitor expand Show data source
Vasodilator expand Show data source
Purity
≥99% (HPLC) expand Show data source
Certificate of Analysis
Download expand Show data source
Application(s)
Antiallergic expand Show data source
Bronchodilator expand Show data source
Cerebral vasodilator expand Show data source
Neuroprotective expand Show data source
Empirical Formula (Hill Notation)
C14 H18 N2 O expand Show data source

DETAILS

DETAILS

DrugBank DrugBank Sigma Aldrich Sigma Aldrich TRC TRC
DrugBank - DB05266 external link
Item Information
Drug Groups approved; investigational
Description Ibudilast is an anti-inflammatory and neuroprotective oral agent which shows an excellent safety profile at 60 mg/day and provides significantly prolonged time-to-first relapse and attenuated brain volume shrinkage in patients with relapsing-remitting (RR) and/or secondary progressive (SP) multiple sclerosis (MS). Ibudilast is currently in development in the U.S. (codes: AV-411 or MN-166), but is approved for use as an antiinflammatory in Japan.
Indication For the treatment of multiple sclerosis, asthma, and cerebrovascular disease.
Toxicity Neuroprotective role of phosphodiesterase inhibitor ibudilast on neuronal cell death induced by activated microglia
Affected Organisms
Humans and other mammals
Half Life 19 hours
External Links
Wikipedia
Sigma Aldrich - I0157 external link
Biochem/physiol Actions
Phosphodiesterase IV (PDE4) inhbitor. Inhibits platelet aggregation. Anti-asthma drug.
Toronto Research Chemicals - I125000 external link
A leukotriene D4 antagonist. Used as an antiallergic, antiasthmatic, and vasodilator (cerebral).

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • • Nishino, K., et al.: Japan J. Pharmacol., 33, 267 (1983)
  • • Ohashi, M., et al.: Arch. Int. Pharmacodyn., 280, 216 (1983)
  • • Armstead, W.M., et al.: J. Pharmacol., Exp. Ther., 244, 138 (1983)
  • • Ger. Pat., 1973, Kyorin Pharm, 2 315 801; CA, 80, 14923s, (synth)
  • • Japan. Pat., 1977, Kyorin Pharm, 77 14 799; CA, 87, 53282w, (synth, pharmacol)
  • • Nagai, H. et al., Jpn. J. Pharmacol., 1983, 33, 1215, (pharmacol)
  • • Mue, S. et al., Arch. Int. Pharmacodyn. Ther., 1986, 283, 153, (pharmacol)
  • • Izumi, Y. et al., Arzneim.-Forsch., 1990, 40, 1300
  • • Yasui, M. et al., J. Int. Med. Res., 1990, 18, 415, (pharmacol)
  • • Ohashi, M. et al., Int. Arch. Allergy Appl. Immunol., 1993, 101, 288, (pharmacol)
  • • Martindale, The Extra Pharmacopoeia, 30th edn., Pharmaceutical Press, 1993, 1140
  • • Souness, J.E. et al., Br. J. Pharmacol., 1994, 111, 1081, (pharmacol)
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PATENTS

PATENTS

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INTERNET

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