TW201238950A - NAMPT and rock inhibitors - Google Patents
NAMPT and rock inhibitors Download PDFInfo
- Publication number
- TW201238950A TW201238950A TW100141323A TW100141323A TW201238950A TW 201238950 A TW201238950 A TW 201238950A TW 100141323 A TW100141323 A TW 100141323A TW 100141323 A TW100141323 A TW 100141323A TW 201238950 A TW201238950 A TW 201238950A
- Authority
- TW
- Taiwan
- Prior art keywords
- phenyl
- dihydro
- isoindole
- carboxamide
- amine
- Prior art date
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- 108010064862 Nicotinamide phosphoribosyltransferase Proteins 0.000 title abstract description 22
- 102000015532 Nicotinamide phosphoribosyltransferase Human genes 0.000 title abstract 3
- 239000011435 rock Substances 0.000 title abstract 3
- 239000003112 inhibitor Substances 0.000 title description 14
- 150000001875 compounds Chemical class 0.000 claims abstract description 52
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 33
- 238000000034 method Methods 0.000 claims abstract description 28
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- -1 N(R5)2 Chemical compound 0.000 claims description 787
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 290
- 125000000217 alkyl group Chemical group 0.000 claims description 223
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- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 151
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- 125000000623 heterocyclic group Chemical group 0.000 claims description 137
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- ADATWPZKWHHCDS-UHFFFAOYSA-N n-[4-[4-(2-hydroxyethyl)piperazine-1-carbonyl]phenyl]-1,3-dihydroisoindole-2-carboxamide Chemical compound C1CN(CCO)CCN1C(=O)C(C=C1)=CC=C1NC(=O)N1CC2=CC=CC=C2C1 ADATWPZKWHHCDS-UHFFFAOYSA-N 0.000 description 1
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- 239000011664 nicotinic acid Substances 0.000 description 1
- 235000020824 obesity Nutrition 0.000 description 1
- 229910052762 osmium Inorganic materials 0.000 description 1
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 description 1
- FILUFGAZMJGNEN-UHFFFAOYSA-N pent-1-en-3-yne Chemical group CC#CC=C FILUFGAZMJGNEN-UHFFFAOYSA-N 0.000 description 1
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- QYSPLQLAKJAUJT-UHFFFAOYSA-N piroxicam Chemical compound OC=1C2=CC=CC=C2S(=O)(=O)N(C)C=1C(=O)NC1=CC=CC=N1 QYSPLQLAKJAUJT-UHFFFAOYSA-N 0.000 description 1
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- ODLMAHJVESYWTB-UHFFFAOYSA-N propylbenzene Chemical compound CCCC1=CC=CC=C1 ODLMAHJVESYWTB-UHFFFAOYSA-N 0.000 description 1
- OSFBJERFMQCEQY-UHFFFAOYSA-N propylidene Chemical group [CH]CC OSFBJERFMQCEQY-UHFFFAOYSA-N 0.000 description 1
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- 238000011084 recovery Methods 0.000 description 1
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- 235000021286 stilbenes Nutrition 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- RAHZWNYVWXNFOC-UHFFFAOYSA-N sulfur dioxide Inorganic materials O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 1
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Classifications
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| RU2013126657A (ru) | 2014-12-27 |
| PE20140913A1 (es) | 2014-08-22 |
| CL2013001340A1 (es) | 2013-09-06 |
| SG10201602857UA (en) | 2016-05-30 |
| US20160031880A1 (en) | 2016-02-04 |
| BR112013012078A2 (pt) | 2019-09-24 |
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| AU2011329233A1 (en) | 2013-05-23 |
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| US10093624B2 (en) | 2018-10-09 |
| UY33726A (es) | 2012-06-29 |
| US9302989B2 (en) | 2016-04-05 |
| CA2816594A1 (en) | 2012-05-24 |
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