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| Product | Description | |
|---|---|---|
| LICHROLUT EN, 40-120 MYM | LICHROLUT EN, 40-120 MYM. Uses: Designed for use in research and industrial production. Additional or Alternative Names: LICHROLUT EN, 40-120 MYM;LICHROLUT(R) EN. Product Category: Heterocyclic Organic Compound. CAS No. 165039-45-2. Purity: 0.96. Product ID: ACM165039452. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Licoagrochalcone a | Licoagrochalcone a. Uses: Designed for use in research and industrial production. Additional or Alternative Names: licoagrochalcone A, CHEMBL229885, LICOAGROCHALCONEA, SCHEMBL632907, DNC007424, LMPK12120068, 3-Prenyl-4,2,4-trihydroxychalcone, 202815-28-9. Product Category: Heterocyclic Organic Compound. CAS No. 202815-28-9. Molecular formula: C20H20O4. Mole weight: 324.370400 [g/mol]. Purity: 0.96. IUPACName: (E)-1-(2,4-dihydroxyphenyl)-3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]prop-2-en-1-one. Canonical SMILES: CC(=CCC1=C(C=CC(=C1)C=CC(=O)C2=C(C=C(C=C2)O)O)O)C. Product ID: ACM202815289. Alfa Chemistry ISO 9001:2015 Certified. | |
| Licochalcone A | Licochalcone A. Group: Biochemicals. Grades: Plant Grade. CAS No. 58749-22-7. Pack Sizes: 20mg. Molecular Formula: C21H22O4, Molecular Weight: 338.4. US Biological Life Sciences. |  Worldwide |
| Licochalcone A | Licochalcone A (LCA), a flavonoid isolated, presents obvious anti-cancer effects, displays broad-spectrum inhibition against UDP-glucuronosyltransferases (UGTs) [1]. Licochalcone A (LCA) exhibits strong inhibitory effects against UGT1A1, 1A3, 1A4, 1A6, 1A7, 1A9, and 2B7 (both IC 50 and K i values lower than 5 μM) [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Licochalcone-A. CAS No. 58749-22-7. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-N0372. |  |
| Licochalcone B | Licochalcone B. Group: Biochemicals. CAS No. 58749-23-8. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Licochalcone C | Licochalcone C could inhibit α-glucosidase , with IC 50 s of <100 nM and 92.43 μM for α-glucosidase and protein tyrosine phosphatase 1B (PTP1B), respectively. Uses: Scientific research. Group: Natural products. CAS No. 144506-14-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N0374. | |
| licodione 2'-O-methyltransferase | As well as licodione [1-(2,4-dihydroxyphenyl)-3-(4-hydroxyphenyl)-1,3-propanedione], the 2''-hydroxy-derivative and isoliquiritigenin can act as acceptors, but more slowly. Group: Enzymes. Enzyme Commission Number: EC 2.1.1.65. CAS No. 77000-07-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1967; licodione 2'-O-methyltransferase; EC 2.1.1.65; 77000-07-8. Cat No: EXWM-1967. |  |
| licodione synthase | A heme-thiolate protein (P-450). It probably forms 2-hydroxyliquiritigenin which spontaneously forms licodione. NADH can act instead of NADPH, but more slowly. Group: Enzymes. Enzyme Commission Number: EC 1.14.13.87. CAS No. 157972-05-9. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0895; licodione synthase; EC 1.14.13.87; 157972-05-9. Cat No: EXWM-0895. | |
| Licofelone | Licofelone (ML-3000) is a dual COX/5-lipoxygenase (5-LOX) inhibitor ( IC 50 =0.21/0.18 μM, respectively) for the treatment of osteoarthritis. Licofelone exerts anti-inflammatory and anti-proliferative effects. Licofelone induces apoptosis , and decreases the production of proinflammatory leukotrienes and prostaglandins [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ML-3000. CAS No. 156897-06-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-B1452. | |
| Licofelone | Licofelone is a dual inhibitor of COX-1/COX-2 and 5-lipoxygenase. Uses: Lipoxygenase inhibitors. Synonyms: ML 3000; ML3000; ML-3000; 6-(4-chlorophenyl)-2,3-dihydro-2,2-dimethyl-7-phenyl-1H-pyrrolizine-5-acetic acid. CAS No. 156897-06-2. Molecular formula: C23H22ClNO2. Mole weight: 379.9. |  |
| Licofelone | Dual inhibitor of cyclooxygenase and 5-lipoxygenase. Anti-inflammatory. Group: Biochemicals. Alternative Names: 6-(4-Chlorophenyl)-2,3-dihydro-2,2-dimethyl-7-phenyl-1H-pyrrolizine-5-acetic Acid; ML-3000. Grades: Highly Purified. CAS No. 156897-06-2. Pack Sizes: 50mg, 100mg, 250mg, 500mg. Molecular Formula: C??H??ClNO?, Molecular Weight: 379.88. US Biological Life Sciences. | Worldwide |
| Licoflavone B | Licoflavone B is a flavonoid isolated from Glycyrrhiza inflata, inhibits S. mansoni ATPase (IC50, 23.78 μM) and ADPase (IC50, 31.50 μM) activity. Anti-schistosomiasis activity. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. Appearance: Solid. CAS No. 91433-17-9. Molecular formula: C25H26O4. Mole weight: 390.47. Purity: 0.9991. Canonical SMILES: O=C1C=C(C2=CC=C(O)C(C/C=C(C)\C)=C2)OC3=CC(O)=C(C/C=C(C)\C)C=C13. Product ID: ACM91433179. Alfa Chemistry ISO 9001:2015 Certified. | |
| Licogliflozin | Licogliflozin is a sodium glucose cotransporter ( SGLT1 and SGLT2 ) inhibitor. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LIK066. CAS No. 1291094-73-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109092. | |
| Licoisoflavone A | Licoisoflavone A. Group: Biochemicals. CAS No. 66056-19-7. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Licorice Extract | Licorice Extract. Applications: As a sweetener, licorice extract is used in food industry;as as raw materials of drugs for clearing heat and detoxicating, licorice extract is used in medicine field;as product for benefiting stomach, licorice extract is widely used in health industry;licorice extract applied in cosmetic field, licorice extract is able to nourish and cure the skin. Group: Others. Purity: 10%-98% Min. Appearance: Brown fine powder. Source: Liquorice, or licorice is the root of Glycyrrhiza glabra from which a sweet flavour can be extracted. The liquorice plant is a herbaceous perennial legume native to southern Europe, India, and parts of Asia. It is not botanically related to anise, star anise, or fennel, which are sources of similar flavouring compounds. Licorice Extract; Radix Glycyrrhizae. Cat No: EXTC-191. | |
| Licorice Root (Glycyrrhiza Glabra) Powder & P.E. < DGL 3% | Licorice Root (Glycyrrhiza Glabra) Powder & P.E. < DGL 3%. |  CA, FL & NJ |
| Lidanserin | Lidanserin (ZK-33839) acts as a 5-HT 2A and α 1 -adrenergic receptor antagonist. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ZK-33839. CAS No. 73725-85-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-101815. | |
| L-Idaric acid | L-Idaric acid is a promising compound for biomedical applications in research of microbial invasions, assuming a prominent role as the chief constituent in studying a diverse gamut of afflictions, ranging from bacterial infections to fungal maladies. Synonyms: L-idaric acid; 80876-58-0; Discontinued See I164930; (2R,3S,4S,5R)-2,3,4,5-tetrahydroxyhexanedioic acid; SCHEMBL15895451; CHEBI:21333; W-203842; Q27109388. CAS No. 80876-58-0. Molecular formula: C6H10O8. Mole weight: 210.14. | |
| L-Idaric acid 1,4-lactone | L-Idaric acid 1,4-lactone, an esteemed biomedicine with a myriad of applications, unveils its profound therapeutic prowess in the vast realm of medical science. Renowned for its exquisite antioxidant attributes and tantalizing potential in combating cancer, this compound entices researchers and drug developers alike, beckoning them to unravel its enigmatic therapeutic effects that navigate the intricate labyrinth of specific malignancies and afflictions tormenting the delicate harmony of oxidative stress-induced conditions. Synonyms: L-Idaro-1,4-lactone. CAS No. 80876-59-1. Molecular formula: C6H8O7. Mole weight: 192.12. | |
| L-Idaric Acid Disodium Salt | L-Idaric acid is used as a reagent to synthesize L-idaro-1,4-lactone, an inhibitor of α-L-idosiduronase. L-Idaric acid is also used as a reagent to biosynthesize myoinositol in rat seminal vesicles. Molecular formula: C6H8Na2O8. Mole weight: 254.1. | |
| L-Iditol | L-Iditol, known as a pharmaceutical excipient and nutrient additive, showcases its versatility in the sphere of medical applications. Its intrinsic stabilizing properties render it a trusted component in tablet and capsule fabrication. Synonyms: L-Iditol; 488-45-9; Iditol; (2S,3R,4R,5S)-hexane-1,2,3,4,5,6-hexol; Hexahydroxyhexane; 1Q2H9GC12E; (2S,3R,4R,5S)-hexane-1,2,3,4,5,6-hexaol; MFCD00064289; Karion; Hexahydric alcohol; L-Idit; IDITOL, L-; L-Iditol, >=98%; UNII-1Q2H9GC12E; SCHEMBL435775; CHEBI:18202; FBPFZTCFMRRESA-UNTFVMJOSA-N; DTXSID901337629; AKOS024258141; AS-56025; HY-121654; CS-0082969; I0725; C01507; D91196; W-202860; Q27102896. CAS No. 488-45-9. Molecular formula: C6H14O6. Mole weight: 182.17. | |
| L-iditol 2-dehydrogenase | This enzyme is widely distributed and has been described in archaea, bacteria, yeast, plants and animals. It acts on a number of sugar alcohols, including (but not limited to) L-iditol, D-glucitol, D-xylitol, and D-galactitol. Enzymes from different organisms or tissues display different substrate specificity. The enzyme is specific to NAD+ and can not use NADP+. Group: Enzymes. Synonyms: polyol dehydrogenase; sorbitol dehydrogenase; L-iditol:NAD+ 5-oxidoreductase; L-iditol (sorbitol) dehydrogenase; glucitol dehydrogenase; L-iditol:NAD+ oxidoreductase; NAD+-dependent sorbitol dehydrogenase; NAD+-sorbitol dehydrogenase. Enzyme Commission Number: EC 1.1.1.14. CAS No. 9028-21-1. SDH. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0043; L-iditol 2-dehydrogenase; EC 1.1.1.14; 9028-21-1; polyol dehydrogenase; sorbitol dehydrogenase; L-iditol:NAD+ 5-oxidoreductase; L-iditol (sorbitol) dehydrogenase; glucitol dehydrogenase; L-iditol:NAD+ oxidoreductase; NAD+-dependent sorbitol dehydrogenase; NAD+-sorbitol dehydrogenase. Cat No: EXWM-0043. | |
| Lidocaine | Lidocaine (Lignocaine) inhibits sodium channels involving complex voltage and using dependence [1]. Lidocaine decreases growth, migration and invasion of gastric carcinoma cells via up-regulating miR-145 expression and further inactivation of MEK/ERK and NF-κB signaling pathways. Lidocaine is an amide derivative and has potential for the research of ventricular arrhythmia [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Lignocaine. CAS No. 137-58-6. Pack Sizes: 10 mM * 1 mL; 500 mg; 5 g; 10 g. Product ID: HY-B0185. | |
| Lidocaine | Lidocaine. Group: Biochemicals. Alternative Names: Xylocaine; Lignocaine. Grades: Highly Purified. CAS No. 137-58-6. Pack Sizes: 100g, 250g, 500g, 1kg, 2kg. Molecular Formula: C14H22N2O. US Biological Life Sciences. | Worldwide |
| Lidocaine Base USP | Lidocaine is a local anesthetic that works by causing temporary numbness/loss of feeling in the skin and mucous membranes. Uses: topically to relieve itching, burning, and pain from inflammatory skin conditions, injected as a dental anesthetic. Group: OTC (Over-the-Counter) Active Ingredients. INCI Name: Lidocaine Base USP. CAS Number: 137-58-6. |  United States and all of its trading partners.. |
| Lidocaine-d10 | Lidocaine-d 10 is the deuterium labeled Lidocaine. Lidocaine (Lignocaine) inhibits sodium channels involving complex voltage and using dependence[1]. Lidocaine decreases growth, migration and invasion of gastric carcinoma cells via up-regulating miR-145 expression and further inactivation of MEK/ERK and NF-κB signaling pathways. Lidocaine is an amide derivative and has potential for the research of ventricular arrhythmia[2]. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 851528-09-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-B0185S1. | |
| Lidocaine-d10 hydrochloride | Lidocaine-d 10 (hydrochloride) is the deuterium labeled Lidocaine hydrochloride. Lidocaine hydrochloride (Lignocaine hydrochloride) inhibits sodium channels involving complex voltage and using dependence[1]. Lidocaine hydrochloride decreases growth, migration and invasion of gastric carcinoma cells via up-regulating miR-145 expression and further inactivation of MEK/ERK and NF-κB signaling pathways. Lidocaine hydrochloride, an amide derivative, has the potential for the research of the ventricular arrhythmia[2]. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 1189959-13-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-B0185AS. | |
| Lidocaine-d10 Hydrochloride (2- (Diethyl-d10-amino) -N- (2, 6-dimethylphenyl) acetamide Hydrochloride, Basicaina-d10, Batixim-d10, Dynexan-d10, Heweneural-d10, Licain-d10) | Anesthetic (local); antiarrhythmic (class IB). Group: Biochemicals. Alternative Names: 2- (Diethyl-d10-amino) -N- (2, 6-dimethylphenyl) acetamide Hydrochloride; Basicaina-d10; Batixim-d10; Dynexan-d10; Heweneural-d10; Licain-d10. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Lidocaine-d10 N-Oxide | A novel labeled metabolite of Lidocaine. Group: Biochemicals. Alternative Names: 2-[Di (ethyl-d5) oxidoamino]-N- (2, 6-dimethylphenyl) acetamide; 2-[Di(ethyl-d5)amino]-2',6'-acetoxylidide N-Oxide; 2-[Di (ethyl-d5) amino]-N- (2, 6-dimethylphenyl) acetamide N2-Oxide. Grades: Highly Purified. CAS No. 851528-10-4. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| Lidocaine-d6 Hydrochloride | Lidocaine-d6 Hydrochloride is the labeled analogue of Lidocaine Hydrochloride, a local anesthetic; antiarrhythmic (class IB). Long-acting, membrane stabilizing agent against ventricular arrhythmia. Originally developed as a local anesthetic. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C14H17D6ClN2O. US Biological Life Sciences. | Worldwide |
| Lidocaine EP Impurity E HCl | Lidocaine EP Impurity E HCl. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1135231-62-7. Molecular Formula: C20H26ClN3O2. Mole Weight: 375.9. Catalog: APB1135231627. |  |
| Lidocaine EP Impurity F | Lidocaine EP Impurity F. Uses: For analytical and research use. Group: Impurity standards. CAS No. 142713-08-4. Molecular Formula: C14H22N2O. Mole Weight: 234.34. Catalog: APB142713084. | |
| Lidocaine EP Impurity G | Lidocaine EP Impurity G. Uses: For analytical and research use. Group: Impurity standards. CAS No. 42459-30-3. Molecular Formula: C13H20N2O. Mole Weight: 220.32. Catalog: APB42459303. | |
| Lidocaine EP Impurity I | Lidocaine EP Impurity I. Uses: For analytical and research use. Group: Impurity standards. CAS No. 17289-53-1. Molecular Formula: C14H22N2O. Mole Weight: 234.34. Catalog: APB17289531. | |
| Lidocaine EP Impurity J | Lidocaine EP Impurity J. Uses: For analytical and research use. Group: Impurity standards. CAS No. 857570-37-7. Molecular Formula: C14H22N2O. Mole Weight: 234.34. Catalog: APB857570377. | |
| Lidocaine EP impurity K (free acid) | Lidocaine EP impurity K (free acid). Uses: For analytical and research use. Group: Impurity standards. CAS No. 74634-66-5. Molecular Formula: C13H20N2O. Mole Weight: 220.32. Catalog: APB74634665. | |
| Lidocaine HCL | Lidocaine HCL. Categories: lidocaine hydrochloride; 73-78-9. | CA, FL & NJ |
| Lidocaine HCL USP | Lidocaine is a local anesthetic that works by causing temporary numbness/loss of feeling in the skin and mucous membranes. Water soluble form of lidocaine. Uses: used topically to relieve itching, burning, and pain from inflammatory skin conditions, injected as a dental anesthetic. Group: OTC (Over-the-Counter) Active Ingredients. INCI Name: Lidocaine HCL. CAS Number: 6108-05-0. | United States and all of its trading partners.. |
| Lidocaine hydrochloride | Lidocaine hydrochloride (Lignocaine hydrochloride) inhibits sodium channels involving complex voltage and using dependence [1]. Lidocaine hydrochloride decreases growth, migration and invasion of gastric carcinoma cells via up-regulating miR-145 expression and further inactivation of MEK/ERK and NF-κB signaling pathways. Lidocaine hydrochloride is an amide derivative and a agent to treat ventricular arrhythmia and an effective tumor-inhibitor [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Lignocaine hydrochloride. CAS No. 73-78-9. Pack Sizes: 10 mM * 1 mL; 500 mg; 5 g; 10 g. Product ID: HY-B0185A. | |
| Lidocaine hydrochloride hydrate | Lidocaine (Lignocaine) hydrochloride hydrate inhibits sodium channels involving complex voltage and using dependence. Lidocaine hydrochloride hydrate decreases growth, migration and invasion of gastric carcinoma cells via up-regulating miR-145 expression and further inactivation of MEK/ERK and NF-κB signaling pathways. Lidocaine hydrochloride hydrate is an amide derivative and has potential for the research of ventricular arrhythmia [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Lignocaine hydrochloride hydrate. CAS No. 6108-05-0. Pack Sizes: 50 mg; 100 mg. Product ID: HY-B0185B. | |
| Lidocaine Hydrochloride Monohydrate | Lidocaine hydrochloride monohydrate is a commonly used as local anesthetic in topical applications and oral mucosal biopsies. It has a short anesthetic half-life; Na+ channel blocker; class IB antiarrhythmic that is rapidly absorbed after parenteral administration. Group: Biochemicals. Alternative Names: 2-(Diethylamino)-2',6'-acetoxylidide Hydrochloride; 2-(Diethylamino)-2',6'-dimethylacetanilide Hydrochloride; Alphacaine; DioCaine; Irtopan; Jetmonal; Lidesthesin; Lidocain Hydrochloride; Lidocaine Monohydrochloride; Lidothesin; Lignavet; Lignocaine Hydrochloride; Luan; Metaclopromide Hydrochloride; Odontalg; Proliferol; Rapidocaine; Sedagul; Versicane; Xilina Hydrochloride; Xycaine Hydrochloride; Xylanaest Purum; Xylocaine Astra; Xylocaine Hydrochloride; Xylocard; Xyloneural; Xylotox. Grades: Highly Purified. CAS No. 6108-05-0. Pack Sizes: 5g, 10g, 25g, 50g, 100g. Molecular Formula: C14H23ClN2O, Molecular Weight: 288.81. US Biological Life Sciences. | Worldwide |
| Lidocaine Impurity 11 | Lidocaine Impurity 11. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C14H19N3. Mole Weight: 229.33. Catalog: APB10769. | |
| Lidocaine Impurity 12 | Lidocaine Impurity 12. Uses: For analytical and research use. Group: Impurity standards. Molecular Formula: C15H22N2O. Mole Weight: 246.35. Catalog: APB10770. | |
| Lidocaine Impurity 1 (2-(Diethylamino)-N-(Diethylaminoyl)acetamide) | | |
| Lidocaine Impurity 13 | Lidocaine Impurity 13. Uses: For analytical and research use. Group: Impurity standards. CAS No. 5177-35-5. Molecular Formula: C10H12ClNO. Mole Weight: 197.66. Catalog: APB5177355. | |
| Lidocaine Impurity 17 | Lidocaine Impurity 17. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 2-chloro-N-(2,6-dimethylphenyl)acetamide. CAS No. 1131-01-7. Molecular Formula: C10H12ClNO. Mole Weight: 197.66. Catalog: APB1131017. | |
| Lidocaine Impurity 2 | Lidocaine Impurity 2. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1596965-85-3. Molecular Formula: C11H23N3O2. Mole Weight: 229.32. Catalog: APB1596965853. | |
| Lidocaine Impurity 2 (2-[(Diethylcarbamoyl)amino]-N, N-Diethylacetamide) | Cas No. 1596965-85-3. | |
| Lidocaine Impurity 3 HCl | | |
| Lidocaine Impurity 4 | Lidocaine Impurity 4. Uses: For analytical and research use. Group: Impurity standards. CAS No. 219500-63-7. Molecular Formula: C10H13NS2. Mole Weight: 211.34. Catalog: APB219500637. | |
| Lidocaine Impurity 5 | Lidocaine Impurity 5. Uses: For analytical and research use. Group: Impurity standards. CAS No. 2903-48-2. Molecular Formula: C10H11NO3. Mole Weight: 193.2. Catalog: APB2903482. | |
| Lidocaine Impurity 6 HCl | Lidocaine Impurity 6 HCl. Uses: For analytical and research use. Group: Impurity standards. CAS No. 857170-05-9. Molecular Formula: C14H23ClN2O. Mole Weight: 270.8. Catalog: APB857170059. | |
| Lidocaine Impurity 7 HCl | Lidocaine Impurity 7 HCl. Uses: For analytical and research use. Group: Impurity standards. CAS No. 77966-82-6. Molecular Formula: C14H23ClN2O. Mole Weight: 270.8. Catalog: APB77966826. | |
| Lidocaine Impurity 8 | Lidocaine Impurity 8. Uses: For analytical and research use. Group: Impurity standards. CAS No. 2315-36-8. Molecular Formula: C6H12ClNO. Mole Weight: 149.62. Catalog: APB2315368. | |
| Lidocaine Impurity 9 | Lidocaine Impurity 9. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1606-01-5. Molecular Formula: C6H13NO2. Mole Weight: 131.18. Catalog: APB1606015. | |
| Lidocaine N-ethyl chloride | Lidocaine N-ethyl chloride. Uses: For analytical and research use. Group: Fluorescence/luminescence spectroscopy. CAS No. 5369-3-9. Pack Sizes: 500MG, 1G. Mole Weight: 298.85. Catalog: AP5369039. | |
| Lidocaine N-Oxide | A novel metabolite of Lidocaine. Group: Biochemicals. Alternative Names: 2- (Diethyloxidoamino) -N- (2, 6-dimethylphenyl) acetamide; 2-(Diethylamino)-2',6'-acetoxylidide N-Oxide; 2- (Diethylamino) -N- (2, 6-dimethylphenyl) acetamide N2-Oxide. Grades: Highly Purified. CAS No. 2903-45-9. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Lidocaine USP | 2-Diethylaminoaceto-2',6'-xylidide; Lignocaine. macular degeneration therapy. Grades: USP. CAS No. 137-58-6. Product ID: 8-04376. Molecular formula: C14H22N2O. Mole weight: 234.34. Properties: white powder mp 215-216°C solubility DMSO 9 mg/mL. |  |
| Lidoflazine | Lidoflazine is a high affinity blocker of the HERG (human ether-a-go-go-related gene) K + channel. Lidoflazine is an antianginal calcium channel blocker that carries a significant risk of QT interval prolongation and ventricular arrhythmia [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 3416-26-0. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-112075. | |
| L-idonate 5-dehydrogenase | The enzyme from the bacterium Escherichia coli is specific for 5-dehydro-D-gluconate. cf. EC 1.1.1.366, L-idonate 5-dehydrogenase (NAD+). Group: Enzymes. Enzyme Commission Number: EC 1.1.1.264. CAS No. 211737-68-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0170; L-idonate 5-dehydrogenase; EC 1.1.1.264; 211737-68-7. Cat No: EXWM-0170. | |
| L-idonate 5-dehydrogenase (NAD+) | Involved in the catabolism of ascorbate (vitamin C) to tartrate. No activity is observed with NADP+ (cf. EC 1.1.1.264, L-idonate 5-dehydrogenase). Group: Enzymes. Enzyme Commission Number: EC 1.1.1.366. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0283; L-idonate 5-dehydrogenase (NAD+); EC 1.1.1.366. Cat No: EXWM-0283. | |
| L-Idonic acid-1,4-lactone | L-Idonic acid-1,4-lactone, a chemical compound with vital biomedical applications, is renowned for its ability to synthesize L-ascorbic acid or vitamin C, a potent micronutrient that functions as a powerful antioxidant in the human body. This compound has tremendous potential to prevent and treat scurvy triggered by vitamin C deficiency. With its multi-faceted therapeutic properties, L-Idonic acid-1,4-lactone stands out as a promising candidate for future research in pharmacology and medicine. CAS No. 1128-24-1. Molecular formula: C6H10O6. Mole weight: 178.14. | |
| L-Idonic acid sodium | L-Idonic acid sodium, an imperative compound in the biomedical sector, finds prevalent usage in the manufacturing of pharmaceutical agents. It assumes a pivotal function in managing specific ailments, namely diabetes and Alzheimer's, through the regulation of glucose metabolism and mitigation of oxidative stress. By virtue of its distinctive characteristics, the profound impact of L-Idonic acid sodium on the progression of biomedical exploration and the creation of efficacious curative measures becomes indisputable. Synonyms: L-idonic acid; Idonic acid; 1114-17-6; (2R,3S,4R,5S)-2,3,4,5,6-pentahydroxyhexanoic acid; Galaktonsaure; SCHEMBL16609822; CHEBI:21336; DTXSID201317688; AKOS040752064; C00770; Q27109389; (2R,3S,4R,5S)-2,3,4,5,6-pentakis(oxidanyl)hexanoic acid. Grades: ≥ 97% (HPLC). CAS No. 1114-17-6. Molecular formula: C6H12O7. Mole weight: 196.16. | |
| L-Idose-1-13C | L-Idose-1-13C. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. Molecular Formula: C513CH12O6, Molecular Weight: 181.15. US Biological Life Sciences. | Worldwide |
| L-Idose-2-13C | L-Idose-2-13C. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. Molecular Formula: C513CH12O6, Molecular Weight: 181.15. US Biological Life Sciences. | Worldwide |
| L-Idose-6-13C | L-Idose-6-13C. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. Molecular Formula: C513CH12O6, Molecular Weight: 181.15. US Biological Life Sciences. | Worldwide |
| L-Idose - Aqueous solution | L-Idose Syrup - Aqueous elixir, an innovative biomedical concoction is an enriching sugar derivative, exhibiting remarkable and auspicious potential in studying an assortment of ailments such as cancer and diabetes. Synonyms: Idose, L-; 5934-56-5; (2R,3S,4R,5S)-2,3,4,5,6-pentahydroxyhexanal; F78BCN2M7Z; aldehydo-L-idose; IDOSE L-FORM [MI]; SCHEMBL16609846; CHEBI:151298; GZCGUPFRVQAUEE-UNTFVMJOSA-N; AKOS027326902; L-Idose-1-13C (0.16M Aqueous Solution); WURCS=2.0/1,1,0/[o2121h]/1/; Q27277756. CAS No. 5934-56-5. Molecular formula: C6H12O6. Mole weight: 180.16. | |
| L-Iduronic acid | L-Iduronic acid, a highly significant compound prevalent in the biomedical field, finds extensive application. In the pursuit of combating diverse ailments like cancer, cardiovascular diseases, and inflammatory disorders, this compound serves as an indispensable component for drug synthesis. Its remarkable attributes render it crucial for formulating drug delivery systems that augment therapeutic efficacy. Synonyms: Iduronic acid, L-; Aldehydo-L-iduronic acid. Grades: ≥95%. CAS No. 2073-35-0. Molecular formula: C6H10O7. Mole weight: 194.14. | |
| L-Iduronic acid-1,6-13C2 | L-Iduronic acid-1,6-13C2 is a valuable biochemical utilized in the biomedical industry for its role in synthesizing drugs used to study diseases related to abnormal glycosaminoglycan metabolism. Its isotopic label, 13C2, aids in research and drug development, facilitating accurate tracing and analysis of metabolic pathways. Molecular formula: 13C2C4H10O7. Mole weight: 2523.81. | |
| L-Iduronic acid sodium salt | L-Iduronic acid sodium salt, a highly significant compound prevalent in the biomedical field, finds extensive application. In the pursuit of combating diverse ailments like cancer, cardiovascular diseases, and inflammatory disorders, this compound serves as an indispensable component for drug synthesis. Its remarkable attributes render it crucial for formulating drug delivery systems that augment therapeutic efficacy. Uses: A constituent of certain mucopolysaccharides. Synonyms: Sodium L-iduronate; L-Iduronic acid, monosodium salt; (2R,3S,4S,5R)-2,3,4,5-tetrahydroxy-6-oxohexanoate sodium salt. Grades: ≥95%. CAS No. 61199-83-5. Molecular formula: C6H9NaO7. Mole weight: 216.12. | |
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