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1. Salicylamide Sodium
2. Salicylamide Sulfate
3. Salicylamide, 3h-labeled
4. Salicylamide, Calcium (2:1) Salt
5. Salicylamide, Monosodium Salt
1. 2-hydroxybenzamide
2. 65-45-2
3. O-hydroxybenzamide
4. Benzamide, 2-hydroxy-
5. Salicylic Acid Amide
6. 2-carbamoylphenol
7. Salamide
8. Urtosal
9. 2-carboxamidophenol
10. Flarpirina
11. Morsarinas
12. Algamon
13. Algiamida
14. Allevin
15. Amidosal
16. Andasol
17. Cetamide
18. Dolomide
19. Dropsprin
20. Eggosalil
21. Liquiprin
22. Novecyl
23. Panithal
24. Raspberin
25. Saliamid
26. Saliamin
27. Salicim
28. Salipur
29. Salizell
30. Salymid
31. Serramida
32. Acket
33. Anamid
34. Oramid
35. Salrin
36. Afko-sal
37. Amid-sal
38. Benzamide, O-hydroxy-
39. Salicilamida
40. Salicilamide
41. Salicylamidum
42. Amid Kyseliny Salicylove
43. Ohb
44. Nsc 3115
45. Mfcd00007978
46. 2-hydroxy-benzamide
47. H.p. 34
48. Sr 4326
49. Nsc-3115
50. Em8bm710zc
51. Chembl27577
52. Mls000069486
53. Chebi:32114
54. Ncgc00091414-02
55. Smr000046394
56. Salicylamide 100 Microg/ml In Acetonitrile
57. Dsstox_cid_1726
58. Dsstox_rid_76295
59. Dsstox_gsid_21726
60. Salizell (van)
61. Benesal (van)
62. Salicilamide [dcit]
63. Salicilamide [italian]
64. Salicylamidum [inn-latin]
65. Cas-65-45-2
66. Salicilamida [inn-spanish]
67. Ccris 6045
68. Hsdb 227
69. Amid Kyseliny Salicylove [czech]
70. Benzoic Acid, 2-hydroxy-, Amide
71. Einecs 200-609-3
72. Unii-em8bm710zc
73. Brn 0742439
74. Salicylamid
75. Samid
76. Ai3-03454
77. Hydroxy Benzamide
78. Saliclamide,(s)
79. Dihydroxybenzalamine
80. 2-oxidanylbenzamide
81. Salicylamide [usp:inn:ban:jan]
82. Salicylamide (tn)
83. Salicylamide, 99%
84. Spectrum_000946
85. Opera_id_1684
86. Spectrum2_001312
87. Spectrum3_000564
88. Spectrum4_000499
89. Spectrum5_001032
90. Salicylamide [mi]
91. Wln: Zvr Bq
92. Salicylamide [inn]
93. Salicylamide [jan]
94. Ec 200-609-3
95. Salicylamide [hsdb]
96. Salicylamide [inci]
97. Nciopen2_001127
98. Salicylamide [vandf]
99. Oprea1_069894
100. Schembl21646
101. Bspbio_001948
102. Kbiogr_001017
103. Kbioss_001426
104. Salicylamide [mart.]
105. 4-10-00-00169 (beilstein Handbook Reference)
106. Divk1c_000858
107. Salicylamide [usp-rs]
108. Salicylamide [who-dd]
109. Spectrum1500532
110. Salicylamide (jan/usp/inn)
111. Spbio_001403
112. Zinc2055
113. Dtxsid3021726
114. Hms502k20
115. Kbio1_000858
116. Kbio2_001426
117. Kbio2_003994
118. Kbio2_006562
119. Kbio3_001448
120. Nsc3115
121. Ninds_000858
122. Hms1920p14
123. Hms2092g15
124. Hms2232e07
125. Pharmakon1600-01500532
126. Component Of Tolagesic (salt/mix)
127. Hy-b0811
128. Salicylamide [usp Monograph]
129. Tox21_111129
130. Tox21_201944
131. Tox21_302801
132. Bbl016007
133. Bdbm50056900
134. Ccg-39250
135. Nsc757318
136. S6404
137. Stk301812
138. Akos000120983
139. Tox21_111129_1
140. Cs-7630
141. Db08797
142. Nsc-757318
143. Idi1_000858
144. Ncgc00091414-01
145. Ncgc00091414-03
146. Ncgc00091414-04
147. Ncgc00091414-05
148. Ncgc00091414-07
149. Ncgc00256376-01
150. Ncgc00259493-01
151. Ds-16216
152. Salicylamide, Puriss., >=99.0% (t)
153. Sbi-0051509.p003
154. Eu-0000058
155. Ft-0659360
156. S0006
157. D01811
158. Ab00052089_12
159. A835120
160. Ah-034/32461056
161. Sr-01000721923
162. Benzoic Acid,2-hydroxy,amide Salicylamide
163. J-509663
164. Q2496906
165. Sr-01000721923-2
166. Brd-k81130846-001-02-6
167. Brd-k81130846-001-12-5
168. Z68590124
169. Salicylamide, United States Pharmacopeia (usp) Reference Standard
170. Salicylamide, Pharmaceutical Secondary Standard; Certified Reference Material
| Molecular Weight | 137.14 g/mol |
|---|---|
| Molecular Formula | C7H7NO2 |
| XLogP3 | 1.3 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 1 |
| Exact Mass | 137.047678466 g/mol |
| Monoisotopic Mass | 137.047678466 g/mol |
| Topological Polar Surface Area | 63.3 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 136 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
Salicylamide, which is not metabolized to salicylate in vivo, has antipyretic, analgesic, and antiinflammatory effects similar to those of salicylate.
Gilman, A.G., T.W. Rall, A.S. Nies and P. Taylor (eds.). Goodman and Gilman's The Pharmacological Basis of Therapeutics. 8th ed. New York, NY. Pergamon Press, 1990., p. 650
SALICYLAMIDE, THE AMIDE OF SALICYLIC ACID, IS NO LONGER AN OFFICIAL DRUG. ITS EFFECTS IN MAN ARE NOT RELIABLE, & ITS USE IS NOT RECOMMENDED. THE SMALL DOSES INCLUDED IN "OVER-THE-COUNTER" ANALGESIC AND SEDATIVE MIXTURES ARE PROBABLY INEFFECTIVE.
Gilman, A. G., L. S. Goodman, and A. Gilman. (eds.). Goodman and Gilman's The Pharmacological Basis of Therapeutics. 6th ed. New York: Macmillan Publishing Co., Inc. 1980., p. 695
THIRD MOST COMMON COMPONENT OF NONPRESCRIPTION HYPNOTIC MIXT IS SODIUM SALICYLAMIDE. DOSE OF 1.3 G HAS SLIGHT SEDATIVE EFFECT; DOSE INCL IN NONPRESCRIPTION PRODUCTS IS 200-380 MG. /SODIUM SALICYLAMIDE/
Gilman, A. G., L. S. Goodman, and A. Gilman. (eds.). Goodman and Gilman's The Pharmacological Basis of Therapeutics. 6th ed. New York: Macmillan Publishing Co., Inc. 1980., p. 369
MEDICATION (VET): DEPRESSES INTESTINAL SMOOTH MUSCLE FUNCTION IN RABBIT & DOG TRIALS. MOST PROMISING INDICATION IN VET MEDICINE MAY BE FOR DOGS WITH CALCIUM PHOSPHATE CONTAINING URINARY CALCULI WHICH ITS COMPLEX GLUCURONIDE METABOLITES MAY HELP SOLUBILIZE.
Rossoff, I.S. Handbook of Veterinary Drugs. New York: Springer Publishing Company, 1974., p. 518
For more Therapeutic Uses (Complete) data for SALICYLAMIDE (10 total), please visit the HSDB record page.
RESULTS OF THE FEW ACCEPTABLE CONTROLLED STUDIES ON SALICYLAMIDE INDICATE THAT THIS AGENT IS MUCH LESS EFFECTIVE THAN ASPIRIN AS ANALGESIC OR ANTIPYRETIC WHEN GIVEN IN SAME DOSE & THEREFORE IS TOO WEAK & UNRELIABLE TO BE USEFUL.
American Medical Association, Council on Drugs. AMA Drug Evaluations. 2nd ed. Acton, Mass.: Publishing Sciences Group, Inc., 1973., p. 265
VET: WARNING: CATS MAY BE VERY SENSITIVE TO TOXIC EFFECT OF THIS DRUG.
Rossoff, I.S. Handbook of Veterinary Drugs. New York: Springer Publishing Company, 1974., p. 518
Dose related GI and CNS disturbances are the most common adverse effects of salicylamide. GI disturbances may include nausea, vomiting, heartburn, anorexia, or diarrhea. CNS disturbances may include dizziness, drowsiness, lightheadedness, faintness, or headache. Flushing, hyperventilation, sweating, dry mouth, rash, and thrombocytopenic purpura have also been reported. Adverse Gi and CNS effects occur infrequently with salicylamide doses occur infrequently with salicylamide doses of 325-650 mg but occur often with higher doses. Tinnitus, ecchymoses, hemorrhagic lesions, leukopenia, or thrombocytopenia may also occur with high doses.
McEvoy, G.K. (ed.). American Hospital Formulary Service - Drug Information 95. Bethesda, MD: American Society of Hospital Pharmacists, Inc., 1995 (Plus Supplements 1995)., p. 1417
3. 3= MODERATELY TOXIC: PROBABLE ORAL LETHAL DOSE (HUMAN) 0.5-5 G/KG, BETWEEN 1 OUNCE AND 1 PINT (OR 1 LB) FOR 70 KG PERSON (150 LB).
Gosselin, R.E., H.C. Hodge, R.P. Smith, and M.N. Gleason. Clinical Toxicology of Commercial Products. 4th ed. Baltimore: Williams and Wilkins, 1976., p. II-138
Anti-Inflammatory Agents, Non-Steroidal
Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. (See all compounds classified as Anti-Inflammatory Agents, Non-Steroidal.)
N - Nervous system
N02 - Analgesics
N02B - Other analgesics and antipyretics
N02BA - Salicylic acid and derivatives
N02BA05 - Salicylamide
WHEN...GIVEN ORALLY...IT IS ABSORBED AND EXCRETED SO RAPIDLY THAT HIGH PLASMA LEVELS ARE NOT OBTAINED. IT DIFFUSES QUICKLY INTO THE VARIOUS BODY TISSUES AND INTO A MUCH GREATER APPARENT VOLUME OF BODY WATER... ANIMAL STUDIES SHOW...DIFFUSION RAPIDLY INTO THE BRAIN.
Di Palma, J. (ed.). Drill's Pharmacology in Medicine. 4th ed. New York: McGraw Hill Book Co., 1971., p. 401
/IN THE RABBIT/ RATE OF TRANSPORT OF FREE DRUG ACROSS BASAL BARRIER WAS BLOOD-FLOW-LIMITED, WHILE TRANSPORT OF THE GLUCURONIDE WAS LIMITED BY TRANSPORT STEP OUT OF EPITHELIAL CELL RATHER THAN BY RATE OF SYNTHESIS.
The Chemical Society. Foreign Compound Metabolism in Mammals. Volume 2: A Review of the Literature Published Between 1970 and 1971. London: The Chemical Society, 1972., p. 424
...WHEN DOSE OF SALICYLAMIDE EXCEEDS ABOUT 1 G...SIGNIFICANT LEVELS OF UNCHANGED DRUG APPEAR IN PLASMA.
American Hospital Formulary Service. Volumes I and II. Washington, DC: American Society of Hospital Pharmacists, to 1984., p. 28:08
BIOAVAILABILITY STUDIES IN HUMAN/S/...INDICATED THAT SODIUM SALICYLAMIDE IN SOLN IS ABSORBED FASTER AFTER ORAL DOSES THAN SALICYLAMIDE IN TABLETS. SEDATIVE EFFECT OCCURRED EARLIER WITH NA SALT THAN WITH SALICYLAMIDE & EXTENT OF SEDATION INCR WITH INCR DOSES OF BOTH COMPD.
The Chemical Society. Foreign Compound Metabolism in Mammals. Volume 5: A Review of the Literature Published during 1976 and 1977. London: The Chemical Society, 1979., p. 25
For more Absorption, Distribution and Excretion (Complete) data for SALICYLAMIDE (9 total), please visit the HSDB record page.
SALICYLAMIDE IS CONJUGATED BY INTESTINAL MUCOSA AFTER ORAL ADMINISTRATION...
American Medical Association, Council on Drugs. AMA Drug Evaluations. 2nd ed. Acton, Mass.: Publishing Sciences Group, Inc., 1973., p. 265
AFTER ADMIN OF SALICYLAMIDE TO CATS NO GLUCURONIDE CONJUGATE COULD BE DETECTED IN URINE. INCR AMT OF SULFURIC ACID ESTER CONJUGATE & SUBSTANTIALLY GREATER AMT OF 2,3-DIHYDROXYBENZAMIDE WERE PRODUCED BY CAT COMPARED WITH RABBIT.
The Chemical Society. Foreign Compound Metabolism in Mammals. Volume 4: A Review of the Literature Published during 1974 and 1975. London: The Chemical Society, 1977., p. 367
SALICYLAMIDE GIVES SALICYLAMIDE-2-BETA-D-GLUCURONIDE & SALICYLAMIDE-2-SULFATE IN MAN. /FROM TABLE/
Goodwin, B.L. Handbook of Intermediary Metabolism of Aromatic Compounds. New York: Wiley, 1976., p. S-3
AFTER ADMIN OF 5 MG/KG SALICYLAMIDE IN 5 MG/KG TYLENOL SUSPENSION, CHILDREN EXCRETED 78% OF DOSE AS SALICYLAMIDE SULFATE; ADULTS 36%. IN ADULTS, GLUCURONIDE WAS MAJOR PRODUCT. GLUCURONIDE CONJUGATION DEFICIENCY IN CHILDREN IS ACCOMPANIED BY A HIGHER RATE OF SULFATE FORMATION.
PMID:830879 ROBERTS ET AL; J PEDIATR 90 (JAN): 130 (1977)
For more Metabolism/Metabolites (Complete) data for SALICYLAMIDE (10 total), please visit the HSDB record page.
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ABOUT THIS PAGE
A Salicylamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Salicylamide, including repackagers and relabelers. The FDA regulates Salicylamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Salicylamide API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Salicylamide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Salicylamide supplier is an individual or a company that provides Salicylamide active pharmaceutical ingredient (API) or Salicylamide finished formulations upon request. The Salicylamide suppliers may include Salicylamide API manufacturers, exporters, distributors and traders.
click here to find a list of Salicylamide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Salicylamide Drug Master File in Japan (Salicylamide JDMF) empowers Salicylamide API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Salicylamide JDMF during the approval evaluation for pharmaceutical products. At the time of Salicylamide JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Salicylamide suppliers with JDMF on PharmaCompass.
Salicylamide Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Salicylamide GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Salicylamide GMP manufacturer or Salicylamide GMP API supplier for your needs.
A Salicylamide CoA (Certificate of Analysis) is a formal document that attests to Salicylamide's compliance with Salicylamide specifications and serves as a tool for batch-level quality control.
Salicylamide CoA mostly includes findings from lab analyses of a specific batch. For each Salicylamide CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Salicylamide may be tested according to a variety of international standards, such as European Pharmacopoeia (Salicylamide EP), Salicylamide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Salicylamide USP).
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