JP2006528142A5 - - Google Patents

Info

Publication number

JP2006528142A5

JP2006528142A5 JP2006520721A JP2006520721A JP2006528142A5 JP 2006528142 A5 JP2006528142 A5 JP 2006528142A5 JP 2006520721 A JP2006520721 A JP 2006520721A JP 2006520721 A JP2006520721 A JP 2006520721A JP 2006528142 A5 JP2006528142 A5 JP 2006528142A5

Authority

JP

Japan

Prior art keywords

carbon atoms

use according

arylalkyl group

moiety

cyclohexylmethyl

Prior art date

2004-07-08

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Pending

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• 150000001875 compounds Chemical class 0.000 claims description 2
• 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 2
• 125000000217 alkyl group Chemical group 0.000 claims 2
• 125000003710 aryl alkyl group Chemical group 0.000 claims 2
• 125000004432 carbon atom Chemical group C* 0.000 claims 2
• 239000002253 acid Substances 0.000 claims 1
• 125000003118 aryl group Chemical group 0.000 claims 1
• 150000007522 mineralic acids Chemical class 0.000 claims 1
• 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
• 125000001624 naphthyl group Chemical group 0.000 claims 1
• 208000004296 neuralgia Diseases 0.000 claims 1
• 208000021722 neuropathic pain Diseases 0.000 claims 1
• 150000007524 organic acids Chemical class 0.000 claims 1
• 239000008194 pharmaceutical composition Substances 0.000 claims 1
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
• 150000003839 salts Chemical class 0.000 claims 1
• QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 description 1