Overview
Lysine (abbreviated as Lys or K) is an α-amino acid with the chemical formula HO2CCH(NH2)(CH2)4NH2. This amino acid is an essential amino acid, which means that humans cannot synthesize it. Its codons are AAA and AAG. Lysine is a base, as are arginine and histidine. The ε-amino group acts as a site for hydrogen binding and a general base in catalysis. Common posttranslational modifications include methylation of the ε-amino group, giving methyl-, dimethyl-, and trimethyllysine. The latter occurs in calmodulin. Other posttranslational modifications include acetylation. Collagen contains hydroxylysine which is derived from lysine by lysyl hydroxylase. O-Glycosylation of lysine residues in the endoplasmic reticulum or Golgi apparatus is used to mark certain proteins for secretion from the cell.
Indication
Supplemental lysine has putative anti-herpes simplex virus activity. There is preliminary research suggesting that it may have some anti-osteoporotic activity.
Associated Conditions
- Weight Loss
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2024/08/30 | Phase 2 | Recruiting | |||
2024/04/23 | Phase 1 | Recruiting | |||
2022/01/27 | Phase 1 | Completed | |||
2018/02/27 | Early Phase 1 | Completed | |||
2018/02/22 | Early Phase 1 | Active, not recruiting | |||
2017/02/24 | Phase 1 | Completed | |||
2016/10/11 | Phase 2 | UNKNOWN | Fundacion Investigacion Interhospitalaria Cardiovascular | ||
2016/04/29 | Phase 1 | Completed | |||
2014/09/17 | Phase 1 | Completed | David Vivas | ||
2013/09/05 | Phase 4 | UNKNOWN | Azienda Ospedaliera San Giovanni Battista |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
Baxter Healthcare Corporation | 0338-0184 | INTRAVENOUS | 464 mg in 100 mL | 4/13/2021 | |
Baxter Healthcare Company | 0338-0210 | INTRAVENOUS | 464 mg in 100 mL | 9/21/2020 | |
Baxter Healthcare Corporation | 0338-0210 | INTRAVENOUS | 464 mg in 100 mL | 9/21/2020 | |
Baxter Healthcare Corporation | 0338-1089 | INTRAVENOUS | 247 mg in 100 mL | 4/13/2021 | |
Baxter Healthcare Corporation | 0338-1099 | INTRAVENOUS | 290 mg in 100 mL | 4/13/2021 | |
ICU Medical Inc. | 0990-7171 | INTRAVENOUS | 1575 mg in 100 mL | 5/4/2022 | |
Baxter Healthcare Corporation | 0338-0194 | INTRAVENOUS | 464 mg in 100 mL | 4/13/2021 | |
Baxter Healthcare Company | 0338-1147 | INTRAVENOUS | 290 mg in 100 mL | 9/21/2020 | |
Baxter Healthcare Corporation | 0338-1147 | INTRAVENOUS | 290 mg in 100 mL | 9/21/2020 | |
Baxter Healthcare Company | 0338-1142 | INTRAVENOUS | 159 mg in 100 mL | 9/21/2020 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
---|---|---|---|
Authorised | 7/25/2019 | ||
Authorised | 7/25/2019 |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
LYSAKARE SOLUTION FOR INFUSION 25G / 25G | SIN16003P | INFUSION, SOLUTION | 25 g/L | 8/31/2020 | |
OLICLINOMEL N4-550 E EMULSION FOR INFUSION | SIN12542P | EMULSION | 1.60 g/l | 5/6/2004 | |
SmofKabiven Emulsion for Infusion | SIN14286P | INJECTION, EMULSION | 9.3g /1000ml | 1/8/2013 | |
KABIVEN PERIPHERAL EMULSION FOR INFUSION | SIN11718P | INJECTION | 1.9 g/l | 11/16/2001 | |
OLICLINOMEL N7-1000 E EMULSION FOR INFUSION | SIN12539P | EMULSION | 2.90 g/l | 5/6/2004 | |
NUTRIFLEX® OMEGA PLUS EMULSION FOR INFUSION | SIN15468P | INJECTION, EMULSION | 2.728g/1000ml | 4/23/2018 | |
PERIOLIMEL N4E Emulsion for Infusion | SIN16888P | EMULSION | 1.99g/L | 10/20/2023 | |
TROPHAMINE INJECTION 10% | SIN07846P | INJECTION | 0.82 g/100 ml | 9/12/1994 | |
AMINOPLASMAL B.BRAUN 10% E SOLUTION FOR INFUSION | SIN15411P | INFUSION, SOLUTION | 8.56g/1000ml | 1/23/2018 | |
NUTRIFLEX® OMEGA SPECIAL B. BRAUN EMULSION FOR INFUSION | SIN16734P | INJECTION, EMULSION | 3.980g/1000ml | 3/7/2023 |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
---|---|---|---|---|---|
No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
---|---|---|---|---|---|
VAMINOLACT I.V. SOLUTION | N/A | N/A | N/A | 10/14/1992 | |
PAN-AMIN G INJ | N/A | N/A | N/A | 5/17/1979 | |
PAN-AMIN G SOLUTION FOR INFUSION 500ML | N/A | otsuka pharmaceutical (h.k.) limited | N/A | N/A | 4/5/2012 |
NUTRINEAL PD4 SOLUTION | N/A | N/A | N/A | 9/9/1999 | |
LA-FLAMING INJ. | N/A | N/A | N/A | 1/28/2010 | |
OLIMEL N9E EMULSION FOR INFUSION | N/A | N/A | N/A | 10/24/2013 | |
NUTRIFLEX OMEGA SPECIAL EMULSION FOR INFUSION | N/A | N/A | N/A | 1/11/2012 | |
SMOFKABIVEN EMULSION FOR INFUSION | N/A | N/A | N/A | 5/26/2011 | |
NUTRIFLEX OMEGA PLUS EMULSION FOR INFUSION | N/A | N/A | N/A | 1/11/2012 | |
AMINOGEN-S SOLUTION FOR INFUSION | N/A | wings pharmaceutical ltd | N/A | N/A | 8/15/2013 |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
Cellula-T oral powder jar | 43995 | Hong Sp & Hs | Medicine | A | 4/13/1993 |
SYNTHAMIN 17 Amino acid 10% with Electrolytes and Glucose 25% 1000mL injection AHB6350 | 19609 | Medicine | A | 9/30/1991 | |
AMINOVEN amino acid 10% solution for infusion 500 mL bottle | 117659 | Medicine | A | 10/22/2007 | |
SMOFKABIVEN amino acids 5.1% / lipids 3.8% / glucose 12.7% / electrolytes 0.7% emulsion for intravenous infusion bag 1970 mL | 180546 | Medicine | A | 1/9/2012 | |
Kids Multi | 329564 | Medicine | A | 2/6/2020 | |
OLICLINOMEL N4-550 E 1000 mL IV emulsion for infusion with electrolytes bag | 136599 | Medicine | A | 9/4/2007 | |
OLICLINOMEL N4-550 E 2500 mL IV emulsion for infusion with electrolytes bag | 141396 | Medicine | A | 9/4/2007 | |
OLIMEL N5-860E Emulsion for intravenous infusion | 197417 | Medicine | A | 8/9/2013 | |
Visdon BRAINBOOK Concentration Support | 371690 | Medicine | A | 7/27/2021 | |
Olimel N12-640 emulsion for intravenous infusion bag. | 303755 | Medicine | A | 7/1/2019 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
2.5% TRAVASOL AMINO ACID INJECTION WITH ELECTROLYTES IN 10% DEXTROSE CLINIMIX | baxter corporation clintec nutrition division | 02013975 | Solution - Intravenous | 145 MG / 100 ML | 12/31/1993 |
CLINIMIX E | baxter corporation | 02013967 | Solution - Intravenous | 290 MG / 100 ML | 12/31/1993 |
TRAVASOL INJ WITHOUT ELECTROLYTES 5.5% | baxter corporation | 00388742 | Solution - Intravenous | 318 MG / 100 ML | 12/31/1978 |
PRIMENE 10%-LIQ IV | clintec nutrition company | 02161192 | Liquid - Intravenous | 1.1 G / 100 ML | 12/31/1995 |
METABOLINE | desbergers ltée, division of technilab inc. | 00086878 | Tablet - Oral | 100 MG | 12/31/1967 |
RENAMIN (AMINO ACIDS) INJECTION | baxter corporation | 02020564 | Solution - Intravenous | 450 MG / 100 ML | 2/2/1996 |
PRIMENE 10% | baxter corporation | 02236875 | Liquid - Intravenous | 1.1 G / 100 ML | 11/14/1997 |
CLINIMIX | baxter corporation | 02013916 | Solution - Intravenous | 246 MG / 100 ML | 12/31/1993 |
4.25% TRAVASOL AMINO ACID INJECTION WITH ELECTROLYTES IN 5% DEXTROSE QUICKMIX | baxter corporation clintec nutrition division | 02014017 | Solution - Intravenous | 246 MG / 100 ML | 12/31/1995 |
TRAVASOL | baxter corporation | 00388769 | Solution - Intravenous | 580 MG / 100 ML | 12/31/1980 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
---|---|---|---|---|---|
No CIMA AEMPS (Spain) approvals found for this drug. |
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Philippines FDA approvals found for this drug. |
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Saudi SFDA approvals found for this drug. |
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Malaysia NPRA approvals found for this drug. |
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
---|---|---|---|---|---|
No UK EMC drug information found for this drug. |
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