Weight | 173.259 g/mol |
---|---|
Formula | C12H15N |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
BICIFADINE (66504-75-4, 71195-57-8)
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- A method for the prediction of the crystal structure of ionic organic compoundsthe crystal structures of o-toluidinium chloride and bromide and polymorphism of bicifadine hydrochloride (CrystEngComm, 2004)
- Characterization of the Antinociceptive Actions of Bicifadine in Models of Acute, Persistent, and Chronic Pain (Journal of Pharmacology and Experimental Therapeutics, 2007)
- Stereocontrolled Synthesis of Trisubstituted Cyclopropanes: Expedient, Atom-Economical, Asymmetric Syntheses of (+)-Bicifadine and DOV21947 (ChemInform, 2006)
- The oral analgesic efficacy of bicifadine hydrochloride in postoperative pain. (The Journal of Clinical Pharmacology, 1982)
- Pharmacokinetics, Disposition, and Metabolism of Bicifadine in Humans (Drug Metabolism and Disposition, 2008)
- Determination of the Polymorphic Forms of Bicifadine Hydrochloride by Differential Scanning CalorimetryThermogravimetric Analysis, X-ray Powder Diffraction, Attenuated Total ReflectanceInfrared Spectroscopy, and Attenuated Total ReflectanceNear-Infrared Spectroscopy (Applied Spectroscopy, 2005)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC=C(C=C1)C23CC2CNC3
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InChIKeyOFYVIGTWSQPCLF-UHFFFAOYSA-N
- Pubchem - BICIFADINE
- Wikipedia - Bicifadine
Bicifadine (DOV-220,075) is a serotonin-norepinephrine-dopamine reuptake inhibitor (SNDRI) discovered at American Cyanamid as an analgesic drug candidate, and licensed to DOV Pharmaceutical in 1998 after American Cyanamid was acquired by Wyeth. In January 2007, Dov licensed the rights to bicifadine to XTL Biopharmaceuticals after bicifadine failed in a Phase III clinical trial for chronic lower back pain. XTL ran a PhaseIIb clinical trial for pain caused by diabetic neuropathy, which failed in 2008; XTL terminated the agreement in 2010.
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Synthesis
Reactant
+
2-(4-methylphenyl)propan-1-amine
(Reductive amination)
Similar Compounds
Biphenyl
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1 alternate name
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CRESYL GLYCIDYL ETHER
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4-METHOXYBIPHENYL
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P-CYMENE
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Diphenyl oxide
(101-84-8)
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(68442-68-2, 122-39-4)
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2-(4-methylphenyl)propan-2-ol
(1197-01-9)
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cinnamaldehyde
(14371-10-9, 104-55-2, 57194-69-1)
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(532-27-4)
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(104-55-2)
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(104-55-2)
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(122-66-7, 38622-18-3)
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N,N-Dimethyl-p-toluidine
(99-97-8)
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(27323-18-8, 11097-69-1, 2051-60-7, 53469-21-9)
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(98-87-3, 29797-40-8)
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1-CHLORONAPHTHALENE
(25586-43-0, 90-13-1)
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(622-97-9, 1319-73-9, 24936-41-2)
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(1335-12-2, 122-97-4, 93842-54-7)
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(140-29-4)
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BENZYL CHLOROFORMATE
(501-53-1)
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(140-67-0)
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(499-75-2)
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ALPHA-PHELLANDRENE
(4221-98-1, 1329-99-3, 99-83-2, 34448-33-4)
1 alternate name
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cinnamyl alcohol
(4407-36-7, 104-54-1)
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CINNAMIC ACID
(621-82-9, 9045-22-1, 140-10-3, 63938-16-9)
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(882-33-7)
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(2210-79-9)
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(99-86-5)
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(99-75-2)
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(882-33-7)
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(122-00-9)
1 alternate name
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(712-09-4)
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Phenethyl isocyanate
(1943-82-4)
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(608-07-1)
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Z-cinnamyl alcohol
(104-54-1, 4510-34-3)
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(16634-82-5)
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(103-29-7, 38888-98-1)
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(140-39-6)
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(622-08-2)
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Thymol methyl ether
(1076-56-8)
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(3012-37-1)
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(7705-14-8, 9003-73-0, 8008-56-8, 65996-98-7, 8008-57-9, 138-86-3, 8028-38-4, 0008008-57-9)
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naphthalene
(91-20-3, 68412-25-9)
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azobenzene
(103-33-3, 17082-12-1, 1080-16-6)
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(93-15-2)
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(3327-51-3, 106-43-4)
1 alternate name
5 safety hazards
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DICYCLOHEXYLAMINE
(101-83-7)
1 alternate name
8 safety hazards
3 suppliers
p-Tolualdehyde
(104-87-0)
1 alternate name
3 safety hazards
3 suppliers
2,4-DICHLOROTOLUENE
(95-73-8)
1 alternate name
3 safety hazards
3 suppliers
1,4-DIETHYLBENZENE
(10565-77-2, 105-05-5)
1 alternate name
3 safety hazards
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2-Methyl-5-vinylpyridine
(140-76-1)
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