| Company Name: |
3B Pharmachem (Wuhan) International Co.,Ltd.
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| Tel: |
821-50328103-801 18930552037 |
| Email: |
3bsc@sina.com |
| Products Intro: |
Product Name:PHCCC;N-Phenyl-7-(hydroxyiMino)cyclopropa[b]chroMen-1a-carboxaMide
Purity:99% HPLC Package:1Mg ; 5Mg;10Mg ;100Mg;250Mg ;500Mg ;1g;2.5g ;5g ;10g
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| Company Name: |
Ascent Scientific
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| Tel: |
4401179829988 |
| Email: |
customerservice@ascentscientific.co.uk |
| Products Intro: |
Product Name:PHCCC
Purity:>98% Package:10mg;50mg Remarks:Selective allosteric potentiator at mGlu4 . Also group I antagonist.
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| Company Name: |
Medi-tech Bioscientific Co., Ltd.
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| Tel: |
0519-83246372 13585352506 |
| Email: |
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| Products Intro: |
Product Name:PHCCC
CAS:1161205-27-1
Purity:98% Package:5mg/10mg/100mg/1g/10g
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| Company Name: |
Shanghai Biopharmaleader Co., Ltd.
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| Tel: |
+86 18721201413 |
| Email: |
sales@biopharmaleader.com |
| Products Intro: |
Product Name:(-)-PHCCC
CAS:1161205-27-1
Purity:98%HPLC Package:10g,100g
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| | N-PHENYL-7-(HYDROXYIMINO)CYCLOPROPA[B]CHROMEN-1A-CARBOXAMIDE Basic information |
| Product Name: | N-PHENYL-7-(HYDROXYIMINO)CYCLOPROPA[B]CHROMEN-1A-CARBOXAMIDE | | Synonyms: | N-PHENYL-7-(HYDROXYIMINO)CYCLOPROPA[B]CHROMEN-1A-CARBOXAMIDE;PHCCC;(1aS,7E,7aS)-7,7a-Dihydro-7-(hydroxyimino)-N-phenylbenzo[b]cyclopropa[e]pyran-1a(1H)-carboxamide;(1aS,7E,7aS)-7-hydroxyimino-N-phenyl-1,7a-dihydrocyclopropa[b]chromene-1a-carboxamide;Benzo[b]cyclopropa[e]pyran-1a(1H)-carboxamide, 7,7a-dihydro-7-(hydroxyimino)-N-phenyl-, (1aS,7E,7aS)- | | CAS: | 1161205-27-1 | | MF: | C17H14N2O3 | | MW: | 294.3 | | EINECS: | | | Product Categories: | Glutamate | | Mol File: | Mol File | ![N-PHENYL-7-(HYDROXYIMINO)CYCLOPROPA[B]CHROMEN-1A-CARBOXAMIDE Structure](StructureFile/ChemBookStructure3/GIF/CB0450874.gif) |
| | N-PHENYL-7-(HYDROXYIMINO)CYCLOPROPA[B]CHROMEN-1A-CARBOXAMIDE Chemical Properties |
| Boiling point | 579.1±50.0 °C(Predicted) | | density | 1.41±0.1 g/cm3(Predicted) | | storage temp. | Store at RT | | pka | 10.79±0.40(Predicted) |
| | N-PHENYL-7-(HYDROXYIMINO)CYCLOPROPA[B]CHROMEN-1A-CARBOXAMIDE Usage And Synthesis |
| Biological Activity | Group I metabotropic glutamate receptor antagonist (IC 50 ~ 3 μ M); 67 times more potent than (S)-4-carboxyphenylglycine ((S)-4-Carboxyphenylglycine). Also a positive allosteric modulator for mGlu 4a ; potentiates L-AP4-mediated inhibition of striatopallidal synaptic transmission in vitro . Displays antiParkinsonian effects in rats in vivo . |
| | N-PHENYL-7-(HYDROXYIMINO)CYCLOPROPA[B]CHROMEN-1A-CARBOXAMIDE Preparation Products And Raw materials |
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