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Asam fenamat

Asam fenamat
Model bola-dan-tongkat asam fenamat
Nama
Nama IUPAC (preferensi)
Asam 2-anilinobenzoat
Nama lain
Asam n-fenilantranilat
Penanda
Model 3D (JSmol)
3DMet (({3DMet))}
ChEBI
ChEMBL
ChemSpider
Nomor EC
IUPHAR/BPS
Nomor RTECS (({value))}
UNII
  • InChI=1S/C13H11NO2/c15-13(16)11-8-4-5-9-12(11)14-10-6-2-1-3-7-10/h1-9,14H,(H,15,16) N
    Key: ZWJINEZUASEZBH-UHFFFAOYSA-N N
  • InChI=1/C13H11NO2/c15-13(16)11-8-4-5-9-12(11)14-10-6-2-1-3-7-10/h1-9,14H,(H,15,16)
    Key: ZWJINEZUASEZBH-UHFFFAOYAQ
  • C1=CC=C(C=C1)NC2=CC=CC=C2C(=O)O
Sifat
C13H11NO2
Massa molar 213,23 g/mol
Kecuali dinyatakan lain, data di atas berlaku pada suhu dan tekanan standar (25 °C [77 °F], 100 kPa).
N verifikasi (apa ini YaYN ?)
Referensi

Asam fenamat adalah sebuah senyawa organik yang, terutama dalam bentuk esternya, disebut fenamat.[1]:458 Ia berfungsi sebagai struktur induk untuk beberapa obat antiinflamasi nonsteroid (NSAID), meliputi asam mefenamat, asam tolfenamat, asam flufenamat, dan asam meklofenamat. Obat-obat ini biasa disebut dengan “turunan asam antranilat” atau “fenamat” karena asam fenamat merupakan turunan dari asam antranilat.[2]:235[3]:17[2]

Asam fenamat dapat disintesis dari asam 2-klorobenzoat dan dapat diubah menjadi akridona.[4]

Referensi

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  1. ^ Gupta, PK. Drug NomenclatureUnited States Adopted Names. Ch 27 in Remington: The Science and Practice of Pharmacy, Vol 1. Eds. David B. Troy, Paul Beringer. Lippincott Williams & Wilkins, 2006 ISBN 9780781746731
  2. ^ a b Sriram D, Yogeeswari P. Medicinal Chemistry, 2nd Edition. Pearson Education India, 2010. ISBN 9788131731444
  3. ^ Auburn University course material. Jack DeRuiter, Principles of Drug Action 2, Fall 2002 1: Non-Steroidal Antiinflammatory Drugs (NSAIDS)
  4. ^ C. F. H. Allen, G. H. W. McKee (1939). "Acridone". Organic Syntheses. 2: 6. doi:10.15227/orgsyn.019.0006. 
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Asam fenamat
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