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1. Acid, Aminoacetic
2. Aminoacetic Acid
3. Calcium Salt Glycine
4. Cobalt Salt Glycine
5. Copper Salt Glycine
6. Glycine Carbonate (1:1), Monosodium Salt
7. Glycine Carbonate (2:1), Monolithium Salt
8. Glycine Carbonate (2:1), Monopotassium Salt
9. Glycine Carbonate (2:1), Monosodium Salt
10. Glycine Hydrochloride
11. Glycine Hydrochloride (2:1)
12. Glycine Phosphate
13. Glycine Phosphate (1:1)
14. Glycine Sulfate (3:1)
15. Glycine, Calcium Salt
16. Glycine, Calcium Salt (2:1)
17. Glycine, Cobalt Salt
18. Glycine, Copper Salt
19. Glycine, Monoammonium Salt
20. Glycine, Monopotassium Salt
21. Glycine, Monosodium Salt
22. Glycine, Sodium Hydrogen Carbonate
23. Hydrochloride, Glycine
24. Monoammonium Salt Glycine
25. Monopotassium Salt Glycine
26. Monosodium Salt Glycine
27. Phosphate, Glycine
28. Salt Glycine, Monoammonium
29. Salt Glycine, Monopotassium
30. Salt Glycine, Monosodium
1. 2-aminoacetic Acid
2. 56-40-6
3. Aminoacetic Acid
4. Glycocoll
5. Aminoethanoic Acid
6. Glycolixir
7. H-gly-oh
8. Glycosthene
9. Padil
10. Aciport
11. Glicoamin
12. Hampshire Glycine
13. L-glycine
14. Amitone
15. Leimzucker
16. Acetic Acid, Amino-
17. Aminoazijnzuur
18. Glycine, Non-medical
19. Sucre De Gelatine
20. Gyn-hydralin
21. Gly (iupac Abbrev)
22. Corilin
23. Glycine [inn]
24. Glycinum [inn-latin]
25. Glicina [inn-spanish]
26. Fema No. 3287
27. Glyzin
28. Gly
29. Acide Aminoacetique [inn-french]
30. Acido Aminoacetico [inn-spanish]
31. Acidum Aminoaceticum [inn-latin]
32. Ccris 5915
33. Hsdb 495
34. Ai3-04085
35. Amino-acetic Acid
36. Mfcd00008131
37. Nsc 25936
38. [14c]glycine
39. 25718-94-9
40. Nsc-25936
41. Chembl773
42. Glycine Iron Sulphate (1:1)
43. Te7660xo1c
44. Chebi:15428
45. Aminoacetate
46. Nsc25936
47. Athenon
48. Glycine-13c
49. Polyglycine
50. Ncgc00024503-01
51. Glicina
52. Dsstox_cid_667
53. Glycine, Free Base
54. Acido Aminoacetico
55. Acide Aminoacetique
56. Dsstox_rid_75720
57. Dsstox_gsid_20667
58. Acidum Aminoaceticum
59. Glykokoll
60. Aminoessigsaeure
61. Hgly
62. Cas-56-40-6
63. Glycine, Labeled With Carbon-14
64. Glycine [usp:inn]
65. Glycine 1.5% In Plastic Container
66. Einecs 200-272-2
67. H2n-ch2-cooh
68. Aminoacetic Acid 1.5% In Plastic Container
69. Unii-te7660xo1c
70. Aminoethanoate
71. 18875-39-3
72. Amino-acetate
73. 2-aminoacetate
74. Glycine;
75. Glycine Usp
76. Glycine Technical
77. [3h]glycine
78. Glycine Usp Grade
79. H-gly
80. L-gly
81. Gly-co
82. Gly-oh
83. L-glycine,(s)
84. [14c]-glycine
85. Corilin (salt/mix)
86. Glycine 1 M Solution
87. Tocris-0219
88. Glycine (h-gly-oh)
89. Glycine [vandf]
90. Nh2ch2cooh
91. Glycine [fhfi]
92. Glycine [hsdb]
93. Glycine [inci]
94. Glycine, >=99%
95. Glycine [fcc]
96. Glycine [jan]
97. Glycine [ii]
98. Glycine [mi]
99. Glycine [mart.]
100. Glycine (jp17/usp)
101. Glycine, 99%, Fcc
102. Glycine [usp-rs]
103. Glycine [who-dd]
104. Biomol-nt_000195
105. Bmse000089
106. Bmse000977
107. Wln: Z1vq
108. Ec 200-272-2
109. Gly-253
110. Glycine [green Book]
111. Gtpl727
112. Ab-131/40217813
113. Glycine [orange Book]
114. Glycine, Electrophoresis Grade
115. Glycine [ep Monograph]
116. Bpbio1_001222
117. Gtpl4084
118. Gtpl4635
119. Glycine [usp Monograph]
120. Dtxsid9020667
121. Bdbm18133
122. Buffer Concentrate, Ph 11.01
123. Azd4282
124. Glycine, >=99.0% (nt)
125. Glycine, 98.5-101.5%
126. Pharmakon1600-01300021
127. Glycine 1000 Microg/ml In Water
128. 2-aminoacetic Acid;aminoacetic Acid
129. Bcp25965
130. Cs-b1641
131. Hy-y0966
132. Zinc4658552
133. Glycine, Acs Reagent, >=98.5%
134. Tox21_113575
135. Glycine, 99%, Natural, Fcc, Fg
136. Nsc760120
137. S4821
138. Stl194276
139. Glycine, Purum, >=98.5% (nt)
140. Glycine, Tested According To Ph.eur.
141. Akos000119626
142. Glycine, For Electrophoresis, >=99%
143. Tox21_113575_1
144. Am81781
145. Ccg-266010
146. Db00145
147. Nsc-760120
148. Glycine, Bioultra, >=99.0% (nt)
149. Glycine, Bioxtra, >=99% (titration)
150. Serine Impurity B [ep Impurity]
151. Glycine, Saj Special Grade, >=99.0%
152. Ncgc00024503-02
153. Ncgc00024503-03
154. Bp-31024
155. Glycine, Vetec(tm) Reagent Grade, 98%
156. Glycine, 0.2m Buffer Solution, Ph 2.5
157. Glycine, 0.2m Buffer Solution, Ph 3.0
158. Glycine, 0.2m Buffer Solution, Ph 3.5
159. Db-029870
160. Ft-0600491
161. Ft-0669038
162. G0099
163. G0317
164. Glycine, Reagentplus(r), >=99% (hplc)
165. A20662
166. C00037
167. D00011
168. D70890
169. M03001
170. L001246
171. Q620730
172. Sr-01000597729
173. Glycine, Certified Reference Material, Tracecert(r)
174. Q-201300
175. Sr-01000597729-1
176. Q27115084
177. B72ba06c-60e9-4a83-a24a-a2d7f465bb65
178. F2191-0197
179. Glycine, European Pharmacopoeia (ep) Reference Standard
180. Z955123660
181. Glycine, Bioultra, For Molecular Biology, >=99.0% (nt)
182. Glycine, United States Pharmacopeia (usp) Reference Standard
183. Benzene, Diethenyl-, Polymer With 2-methyl-1,3-butadiene, Hydrogenated
184. Glycine, Pharmaceutical Secondary Standard; Certified Reference Material
185. Glycine, Analytical Standard, For Nitrogen Determination According To Kjeldahl Method
186. Tris-tricine Buffer; Tris-glycine Buffer;tris Glycine Buffer Concentrate;h-gly-oh
187. Glycine, From Non-animal Source, Meets Ep, Jp, Usp Testing Specifications, Suitable For Cell Culture, >=98.5%
188. Glycine, Meets Analytical Specification Of Ph. Eur., Bp, Usp, 99-101% (based On Anhydrous Substance)
189. Glycine, Pharmagrade, Ajinomoto, Ep, Jp, Usp, Manufactured Under Appropriate Gmp Controls For Pharma Or Biopharmaceutical Production, Suitable For Cell Culture
190. Glycine, Puriss. P.a., Reag. Ph. Eur., Buffer Substance, 99.7-101% (calc. To The Dried Substance)
| Molecular Weight | 75.07 g/mol |
|---|---|
| Molecular Formula | C2H5NO2 |
| XLogP3 | -3.2 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 1 |
| Exact Mass | 75.032028402 g/mol |
| Monoisotopic Mass | 75.032028402 g/mol |
| Topological Polar Surface Area | 63.3 Ų |
| Heavy Atom Count | 5 |
| Formal Charge | 0 |
| Complexity | 42.9 |
| 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 |
AMINOACETIC ACID HAS BEEN OCCASIONALLY USED IN THERAPY OF MYASTHENIA GRAVIS BUT MOST INVESTIGATORS DOUBT THAT THE CMPD HAS ANY VALUE IN THIS DISORDER. ... /IT/ IS ALSO USED IN...ANTACID PREPN, SOMETIMES AS A COMPLEX SALT. HOWEVER.../IT HAS/ LIMITED BUFFERING CAPACITY...
Osol, A. and J.E. Hoover, et al. (eds.). Remington's Pharmaceutical Sciences. 15th ed. Easton, Pennsylvania: Mack Publishing Co., 1975., p. 963
AMINOACETIC ACID IS USED IN...1.1% SOLN AS AN IRRIGATING FLUID IN TRANSURETHRAL RESECTION OF THE PROSTATE. ALTHOUGH A 2.1% SOLN...IS ISOTONIC, IT HAS BEEN FOUND THAT A 1.1% SOLN IS NONHEMOLYTIC.
American Hospital Formulary Service. Volumes I and II. Washington, DC: American Society of Hospital Pharmacists, to 1984., p. 40:36
USUALLY FROM 10-15 L OF AMINOACETIC ACID SOLN ARE REQUIRED FOR IRRIGATION DURING TRANSURETHRAL RESECTION OF PROSTATE.
American Hospital Formulary Service. Volumes I and II. Washington, DC: American Society of Hospital Pharmacists, to 1984., p. 40:36
MEDICATION (VET): IV USE IN DOGS INCREASES THEIR TOLERANCE AGAINST CERTAIN TOXIC PARENTERAL AMINO ACID MIXT.
Rossoff, I.S. Handbook of Veterinary Drugs. New York: Springer Publishing Company, 1974., p. 244
For more Therapeutic Uses (Complete) data for GLYCINE (8 total), please visit the HSDB record page.
Supplemental glycine may have antispastic activity. Very early findings suggest it may also have antipsychotic activity as well as antioxidant and anti-inflammatory activities.
Helps trigger the release of oxygen to the energy requiring cell-making process; Important in the manufacturing of hormones responsible for a strong immune system.
Glycine Agents
Substances used for their pharmacological actions on glycinergic systems. Glycinergic agents include agonists, antagonists, degradation or uptake inhibitors, depleters, precursors, and modulators of receptor function. (See all compounds classified as Glycine Agents.)
B - Blood and blood forming organs
B05 - Blood substitutes and perfusion solutions
B05C - Irrigating solutions
B05CX - Other irrigating solutions
B05CX03 - Glycine
Absorption
Absorbed from the small intestine via an active transport mechanism.
Hepatic
In the CNS, there exist strychnine-sensitive glycine binding sites as well as strychnine-insensitive glycine binding sites. The strychnine-insensitive glycine-binding site is located on the NMDA receptor complex. The strychnine-sensitive glycine receptor complex is comprised of a chloride channel and is a member of the ligand-gated ion channel superfamily. The putative antispastic activity of supplemental glycine could be mediated by glycine's binding to strychnine-sensitive binding sites in the spinal cord. This would result in increased chloride conductance and consequent enhancement of inhibitory neurotransmission. The ability of glycine to potentiate NMDA receptor-mediated neurotransmission raised the possibility of its use in the management of neuroleptic-resistant negative symptoms in schizophrenia.
Animal studies indicate that supplemental glycine protects against endotoxin-induced lethality, hypoxia-reperfusion injury after liver transplantation, and D-galactosamine-mediated liver injury. Neutrophils are thought to participate in these pathologic processes via invasion of tissue and releasing such reactive oxygen species as superoxide. In vitro studies have shown that neutrophils contain a glycine-gated chloride channel that can attenuate increases in intracellular calcium and diminsh neutrophil oxidant production. This research is ealy-stage, but suggests that supplementary glycine may turn out to be useful in processes where neutrophil infiltration contributes to toxicity, such as ARDS.
HYPERPOLARIZATION OF MOTONEURONS PRODUCED BY IONTOPHORETIC APPLICATION OF GLYCINE IS RELATIVELY TRANSIENT BUT APPROACHES THE EQUILIBRIUM POTENTIAL FOR THE INDIRECTLY ACTIVATED INHIBITORY POSTSYNAPTIC POTENTIAL...TESTS WITH GABA... INDICATE SIMILAR ELECTROPHYSIOLOGICAL EFFECTS & SIMILAR INCR IN CL- CONDUCTANCE.
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. 247
MAJOR EVIDENCE THAT FAVORS GLYCINE AS MEDIATOR OF INTRASPINAL POSTSYNAPTIC INHIBITION IS THE SELECTIVE ANTAGONISM OF ITS EFFECTS BY STRYCHNINE. ... GLYCINE ALSO APPEARS TO BE MOST LIKELY TRANSMITTER FOR INHIBITORY INTERNEURONS IN RETICULAR FORMATION BUT NOT IN CUNEATE NUCLEUS.
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. 247
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| Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
|---|---|---|---|
| INDIA | 1,19,68,119.61 | 7.6 | > 200 |
| UNITED STATES | 81,27,579.15 | 5.7 | > 200 |
| INDIA | 20,21,588.49 | 14.2 | 51 - 200 |
| INDIA | 7,546.00 | 48.0 | 51 - 200 |
| SOUTH AFRICA | 8,045.00 | 17.1 | 51 - 200 |
| INDIA | 1,830.00 | 63.6 | 11 - 50 |
| INDIA | 4,857.19 | 17.0 | 11 - 50 |
| SINGAPORE | 2,00,806.00 | 8.8 | 11 - 50 |
| MEXICO | 1,31,372.00 | 3.6 | 11 - 50 |
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ABOUT THIS PAGE
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PharmaCompass offers a list of Glycine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Glycine manufacturer or Glycine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Glycine manufacturer or Glycine supplier.
PharmaCompass also assists you with knowing the Glycine API Price utilized in the formulation of products. Glycine API Price is not always fixed or binding as the Glycine Price is obtained through a variety of data sources. The Glycine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A H2N-CH2-COOH manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of H2N-CH2-COOH, including repackagers and relabelers. The FDA regulates H2N-CH2-COOH manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. H2N-CH2-COOH 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 H2N-CH2-COOH manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A H2N-CH2-COOH supplier is an individual or a company that provides H2N-CH2-COOH active pharmaceutical ingredient (API) or H2N-CH2-COOH finished formulations upon request. The H2N-CH2-COOH suppliers may include H2N-CH2-COOH API manufacturers, exporters, distributors and traders.
click here to find a list of H2N-CH2-COOH suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A H2N-CH2-COOH DMF (Drug Master File) is a document detailing the whole manufacturing process of H2N-CH2-COOH active pharmaceutical ingredient (API) in detail. Different forms of H2N-CH2-COOH DMFs exist exist since differing nations have different regulations, such as H2N-CH2-COOH USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A H2N-CH2-COOH DMF submitted to regulatory agencies in the US is known as a USDMF. H2N-CH2-COOH USDMF includes data on H2N-CH2-COOH's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The H2N-CH2-COOH USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of H2N-CH2-COOH suppliers with USDMF 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 H2N-CH2-COOH Drug Master File in Japan (H2N-CH2-COOH JDMF) empowers H2N-CH2-COOH 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 H2N-CH2-COOH JDMF during the approval evaluation for pharmaceutical products. At the time of H2N-CH2-COOH 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 H2N-CH2-COOH suppliers with JDMF on PharmaCompass.
A H2N-CH2-COOH CEP of the European Pharmacopoeia monograph is often referred to as a H2N-CH2-COOH Certificate of Suitability (COS). The purpose of a H2N-CH2-COOH CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of H2N-CH2-COOH EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of H2N-CH2-COOH to their clients by showing that a H2N-CH2-COOH CEP has been issued for it. The manufacturer submits a H2N-CH2-COOH CEP (COS) as part of the market authorization procedure, and it takes on the role of a H2N-CH2-COOH CEP holder for the record. Additionally, the data presented in the H2N-CH2-COOH CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the H2N-CH2-COOH DMF.
A H2N-CH2-COOH CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. H2N-CH2-COOH CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of H2N-CH2-COOH suppliers with CEP (COS) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing H2N-CH2-COOH as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for H2N-CH2-COOH API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture H2N-CH2-COOH as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain H2N-CH2-COOH and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a H2N-CH2-COOH NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of H2N-CH2-COOH suppliers with NDC on PharmaCompass.
H2N-CH2-COOH 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 H2N-CH2-COOH 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 H2N-CH2-COOH GMP manufacturer or H2N-CH2-COOH GMP API supplier for your needs.
A H2N-CH2-COOH CoA (Certificate of Analysis) is a formal document that attests to H2N-CH2-COOH's compliance with H2N-CH2-COOH specifications and serves as a tool for batch-level quality control.
H2N-CH2-COOH CoA mostly includes findings from lab analyses of a specific batch. For each H2N-CH2-COOH 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.
H2N-CH2-COOH may be tested according to a variety of international standards, such as European Pharmacopoeia (H2N-CH2-COOH EP), H2N-CH2-COOH JP (Japanese Pharmacopeia) and the US Pharmacopoeia (H2N-CH2-COOH USP).
