By A. Kleemann, J. Engel

Pharmaceutical components 4th variation has been revised and elevated to incorporate an extra ninety six pharmaceutical compounds, delivering a compendium of over 2200 pharmaceutical components of curiosity to the pharmaceutical and chemical industry.

Pharmaceutical elements is designed to be an entire reference consultant to each pharmaceutical compound of value, offering a wealth of knowledge now not present in the other source including:

- precise artificial path together with intermediates

- alternate names and advertising and marketing facts

- patent details

It is vital as a primary aspect of reference not just for experts in drug chemistry but in addition for a person interested by the selling, sale and use of prescription drugs and pharmaceutical ingredients.

The description of every compound includes:

- Chemical constitution

- Graphical illustration of man-made course together with intermediates

- Nomenclature: resort general, trivial names, synonyms, CAS quantity

- ATC codes

- scientific applications/Therapeutic class

- Toxicological information

- Patent quantity, starting place, holder and expiry date

- advertisement info

- Bibliographic details together with CASSI codes

Of additional price are the indexes of compound sessions, intermediates, exchange names and enzymes, microorganisms, crops and animal tissues.

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Extra resources for Pharmaceutical Substances. Syntheses, Patents, Applications

Example text

1977; prior. 1976). pharmaceutical formulation: JP-appl. 78 136 512 (Chugai; appl. 1977). 1979; J-prior. 1977) use as anti-inflammatory: FX 2 389 377 (J. Brohult, appl. 1977). Formulation(s): amp. 002 mg; cps. 0025 mg, 1 mg; inj. ) 55 A 56 Alfaxalone ride etherote alfaxalone (I) lead tetraacetate Alfodolane ocetote (4. HBr. CH,OH H3C4&, bromine patossium acetate acetone Reference(s): DE 2 030 402 (Glaxo; appl. 1970; GB-prior. 1970). ZA 703 861 (Glaxo; appl. 1970; GB-prior. 1969) (alternative synthesis).

1980; GB-prior. 1974). GB 1 523 865 (Burroughs Wellcome; GB-prior. 1974). c GB 1 567 671 (Wellcome; appl. 1977; USA-prior. 1976). Matsumoto, H. : Chem. Pharm. Bull. (CPBTAL) 36, 1153 (1988). f EP709 385 (Roche; appl. 1995; USA-prior. 1995). 1990; DK-prior. 1989). alternative synthesis via formylguanine: WO 9 507 281 (Recordati; appl. 1994; I-prior. 1993) synthesis using 1,3-dioxolane: US 5 567 816 (Syntex; appl. 1995; USA-prior. 1994). improved procedures: DE 19 536 164 (Boehringcr Ingelheim; D-prior.

500 pglml; inj. sol. I mgl2 ml, 5 mg/lO ml; intensive care inj. 46 (+)-N-[3-[(4-amino-6,7-dimethoxy-2-quinazalinyl)methylamino]propyl]tetrahydro-2-furancarboxamide monohydrochloride RN: 81403-68-1 MF: C19H27N504. 92 OHCaO-CH~ ,OHC~~'~~: , . 1982; F-prior. 1978). DE 290 445 (Synthelabo; appl. 1979; F-prior. 1978). M. : J. Med. Chem. (JMCMAR) 29, 19 (1986). : J. Med. Chem. (JMCMAR) 20, 146 (1977). Formulation(s): tabl. 47 EINECS: 209-869-2 Alibendol 16-dehydroprogesterone 16u, 17a-dihydroxyprogesterone I A (I) -------------, acetophenone 1 Algestone acetophenide I Reference(s): DE 1 125 423 ( O h Mathieson; appl.

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