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| Product | Description | |
|---|---|---|
| cysteine-conjugate transaminase | A number of cysteine conjugates can also act. Group: Enzymes. Synonyms: cysteine conjugate aminotransferase; cysteine-conjugate α-ketoglutarate transaminase (CAT-1). Enzyme Commission Number: EC 2.6.1.75. CAS No. 117698-05-2. 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-2915; cysteine-conjugate transaminase; EC 2.6.1.75; 117698-05-2; cysteine conjugate aminotransferase; cysteine-conjugate α-ketoglutarate transaminase (CAT-1). Cat No: EXWM-2915. |  |
| cysteine-S-conjugate β-lyase | A pyridoxal-phosphate protein. The enzyme can act on a broad range of L-cysteine-S-conjugates, including aromatic conjugates such as 4-bromobenzene and 2,4-dinitrobenzene. The enzyme cleaves a carbon-sulfur bond, releasing a thiol and an unstable enamine product that tautomerizes to an imine form, which undergoes a hydrolytic deamination to form pyruvate and ammonia. The latter reaction, which can occur spontaneously, can also be catalysed by EC 3.5.99.10, 2-iminobutanoate/2-iminopropanoate deaminase. Group: Enzymes. Synonyms: cysteine conjugate β-lyase; glutamine transaminase K/cysteine conjugate β-lyase; L-cysteine-S-conjugate thiol-lyase (deaminating). Enzyme Commission Number: EC 4.4.1.13. CAS No. 68652-57-3. 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-5315; cysteine-S-conjugate β-lyase; EC 4.4.1.13; 68652-57-3; cysteine conjugate β-lyase; glutamine transaminase K/cysteine conjugate β-lyase; L-cysteine-S-conjugate thiol-lyase (deaminating). Cat No: EXWM-5315. | |
| cysteine-S-conjugate N-acetyltransferase | S-Benzyl-L-cysteine and, in decreasing order of activity, S-butyl-L-cysteine, S-propyl-L-cysteine, O-benzyl-L-serine and S-ethyl-L-cysteine, can act as acceptors. Group: Enzymes. Enzyme Commission Number: EC 2.3.1.80. CAS No. 81725-80-6. 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-2261; cysteine-S-conjugate N-acetyltransferase; EC 2.3.1.80; 81725-80-6. Cat No: EXWM-2261. | |
| Prasugrel Cysteine Conjugate Metabolite (R-119251, Mixture of Diastereomers) | A metabolite of Prasugrel.Prasugrel is a platelet inhibitor. It can be used to prevent formation of blood clots. Grades: > 95%. Molecular formula: C21H25FN2O5S2. Mole weight: 468.57. |  |
| Cys(Npys)-(D-Arg)9 | It is a peptide consisting of 9 D-arginine residues and one activated cysteine residue C(Npys), where Npys is 3-Nitro-2-pyridinesulfenyl group protects cysteine. This modification has been used to make the peptide suitable for conjugation and cell permeability studies as a carrier peptide. The S(Npys) group of this cysteine-containing 9R is capable of reacting selectively with the free thiol group of another cysteine-containing peptide to form an unsymmetrical disulfide bond. Synonyms: H-Cys(Npys)-D-Arg-D-Arg-D-Arg-D-Arg-D-Arg-D-Arg-D-Arg-D-Arg-D-Arg-NH2; S-(3-nitropyridin-2-yl)sulfanyl-D-cysteinyl-D-arginyl-D-arginyl-D-arginyl-D-arginyl-D-arginyl-D-arginyl-D-arginyl-D-arginyl-D-argininamide. Grades: ≥95%. Molecular formula: C62H118N40O12S2. Mole weight: 1679.99. | |
| Cys(Npys)-TAT (47-57) | Cys(Npys)-TAT (47-57), corresponding to the protein transduction domain of TAT protein, is synthesized from the activated cysteine residue C(Npys), where Npys is 3-Nitro-2-pyridinesulfenyl group that activates cysteine S and reacts rapidly when thiol groups are introduced. This modification has been used to make the peptide suitable for conjugation studies as a cell-penetrating and carrier peptide. Synonyms: Cys(Npys)-Tyr-Gly-Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg-NH2. Grades: ≥95%. Molecular formula: C72H126N36O16S2. Mole weight: 1816.13. | |
| Cys(Npys)-TAT (47-57), FAM-labeled | It corresponds to the protein transduction domain of the TAT protein and is synthesized with an activated cysteine residue C(Npys), where Npys is 3-Nitro-2-pyridinesulfenyl group and is used for activating S of cysteine and for rapid reaction when a thiol group is introduced. It is synthesized with C(Npys) at the N-terminus for applications requiring specific conjugation reactions and has a fluorophore labeled with FAM having Abs/Em=494/518 nm. This kind of modification has been used to render this peptide as a cell penetrating and carrier peptide applicable in conjugation studies. Synonyms: Cys(Npys)-Tyr-Gly-Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg-Lys(FAM)-NH2. Grades: ≥95%. Molecular formula: C99H148N38O23S2. Mole weight: 2302.61. | |
| DCIA | DCIA is a fluorescent dye. DCIA contains a coumarin fluorophore and conjugates specifically with free cysteines in the protein [1]. Uses: Scientific research. Group: Fluorescent dye. CAS No. 76877-34-4. Pack Sizes: 5 mg; 10 mg. Product ID: HY-D0078. |  |
| Fmoc-Cys((S)-2,3-di(palmitoyloxy)-propyl)-OH | SPPS employing the pure stereoisomer of Fmoc-Pam2Cys-OH allows to obtain more homogeneous lipopeptides. The configuration of bis-palmitoyloxypropy moiety can affect the biological activity of peptide conjugation. Synonyms: Fmoc-(S)Pam2Cys-OH; Fmoc-Cys(Pam)2-OH(S); N-alpha-(fluoren-9-ylmethoxycarbonyl)-S-[2,3-bis(palmitoyloxy)-(2R)-propyl]-(R)-cysteine; Hexadecanoic acid, 1, 1'-[ (1S) -1-[[[ (2R) -2-carboxy-2-[[ (9H-fluoren-9-ylmethoxy) carbonyl]amino]ethyl]thio]methyl]-1, 2-ethanediyl] ester; S-[(2S)-2,3-Bis(palmitoyloxy)propyl]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-cysteine; (2R,6S)-2-(9-Fluorenylmethoxycarbonyl)amino-6,7-bis(palmitoyloxy)-4-thiaheptanic acid. Grades: ≥95%. CAS No. 139573-78-7. Molecular formula: C53H83NO8S. Mole weight: 894.31. | |
| [Fmoc-Lys(Fmoc)]2-Lys-Cys(Acm)-βAla-WangResin | Multiple Antigen Peptide (MAP) resins provide a branching core matrix for preparing synthetic peptide antigens. MAP peptides produced on these resins are utilized as synthetic vaccines and to produce antipeptide antibodies. Incorporation of a cysteine residue into the core matrix allows MAPs with different epitopes to be linked by a disulfide bond. Uses: By incorporating a cysteine residue into the core matrix, map peptides may be conjugated with additional antigens, tags, linkers or biomolecules. Group: Multiple antigen peptide (map) resins. Pack Sizes: 250mg, 1g. |  |
| [Fmoc-Lys(Fmoc)]4-Lys2-Lys-βAla-WangResin | Multiple Antigen Peptide (MAP) resins provide a branching core matrix for preparing synthetic peptide antigens. MAP peptides produced on these resins are utilized as synthetic vaccines and to produce antipeptide antibodies. Incorporation of a cysteine residue into the core matrix allows MAPs with different epitopes to be linked by a disulfide bond. Uses: By incorporating a cysteine residue into the core matrix, map peptides may be conjugated with additional antigens, tags, linkers or biomolecules. Group: Multiple antigen peptide (map) resins. Pack Sizes: 250mg, 1g. | |
| [Fmoc-Lys(Fmoc)]4-Lys2-Lys-Cys(Acm)-βAla-WangResin | Multiple Antigen Peptide (MAP) resins provide a branching core matrix for preparing synthetic peptide antigens. MAP peptides produced on these resins are utilized as synthetic vaccines and to produce antipeptide antibodies. Incorporation of a cysteine residue into the core matrix allows MAPs with different epitopes to be linked by a disulfide bond. Uses: By incorporating a cysteine residue into the core matrix, map peptides may be conjugated with additional antigens, tags, linkers or biomolecules. Group: Multiple antigen peptide (map) resins. Pack Sizes: 250mg, 1g. | |
| HECT-type E3 ubiquitin transferase | In the first step the enzyme transfers ubiquitin from the E2 ubiquitin-conjugating enzyme (EC 2.3.2.23) to a cysteine residue in its HECT domain (which is located in the C-terminal region), forming a thioester bond. In a subsequent step the enzyme transfers the ubiquitin to an acceptor protein, resulting in the formation of an isopeptide bond between the C-terminal glycine residue of ubiquitin and the ε-amino group of an L-lysine residue of the acceptor protein. Group: Enzymes. Synonyms: HECT E3 ligase (misleading); ubiquitin transferase HECT-E3. Enzyme Commission Number: EC 2.3.2.26. 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-2300; HECT-type E3 ubiquitin transferase; EC 2.3.2.26; HECT E3 ligase (misleading); ubiquitin transferase HECT-E3. Cat No: EXWM-2300. | |
| I-152 | I-152 is a conjugate containing N-acetyl-cysteine (NAC) and cysteamine (MEA). I-152 activates NRF2 and ATF4 signals. I-152 has anti-proliferative properties [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 311343-11-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-153340. | |
| N6-Trifluoroacetyl-L-lysine | A cysteine conjugate metabolite adduct formation with specific mitochondrial proteins using antibodies raised against halothane metabolite adducts. Group: Biochemicals. Alternative Names: N6-(2,2,2-Trifluoroacetyl)-. Grades: Highly Purified. CAS No. 10009-20-8. Pack Sizes: 2.5g. US Biological Life Sciences. |  Worldwide |
| N-acyl-aliphatic-L-amino acid amidohydrolase | Contains Zn2+. The enzyme is found in animals and is involved in the hydrolysis of N-acylated or N-acetylated amino acids (except L-aspartate). It acts on mercapturic acids (S-conjugates of N-acetyl-L-cysteine) and neutral aliphatic N-acyl-α-amino acids. Some bacterial aminoacylases demonstrate substrate specificity of both EC 3.5.1.14 and EC 3.5.1.114. cf. EC 3.5.1.15, aspartoacylase and EC 3.5.1.114, N-acyl-aromatic-L-amino acid amidohydrolase. Group: Enzymes. Synonyms: aminoacylase 1; aminoacylase I; dehydropeptidase II; histozyme; hippuricase; benzamidase; acylase I; hippurase; amido acid deacylase; L-aminoacylase; acylase; aminoacylase; L-amino-acid acylase; α-N-acylaminoacid hydrolase; long acyl amidoa. Enzyme Commission Number: EC 3.5.1.14. CAS No. 9012-37-7. ACY1. 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-4403; N-acyl-aliphatic-L-amino acid amidohydrolase; EC 3.5.1.14; 9012-37-7; aminoacylase 1; aminoacylase I; dehydropeptidase II; histozyme; hippuricase; benzamidase; acylase I; hippurase; amido acid deacylase; L-aminoacylase; acylase; aminoacylase; L-amino-acid acylase; α-N-acylaminoacid hydrolase; long acyl amidoacylase; short acyl amidoacylase; ACY1 (gene name); N-acyl-L-amino-acid amidohydrolase. Cat No: EXWM-4403. | |
| N-acyl-aromatic-L-amino acid amidohydrolase | This enzyme is found in animals and is involved in the hydrolysis of N-acylated or N-acetylated amino acids (except L-aspartate). It preferentially deacetylates Nα-acetylated aromatic amino acids and mercapturic acids (S-conjugates of N-acetyl-L-cysteine) that are usually not deacetylated by EC 3.5.1.14, N-acyl-aliphatic-L-amino acid amidohydrolase. The enzyme is significantly activated by Co2+ and Ni2+. Some bacterial aminoacylases demonstrate substrate specificity for both EC 3.5.1.14 and EC 3.5.1.114. cf. EC 3.5.1.14, N-acyl-aliphatic-L-amino acid amidohydrolase and EC 3.5.1.15, aspartoacylase. Group: Enzymes. Synonyms: aminoacylase 3; aminoacylase III; ACY3 (gene name). Enzyme Commission Number: EC 3.5.1.114. 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-4394; N-acyl-aromatic-L-amino acid amidohydrolase; EC 3.5.1.114; aminoacylase 3; aminoacylase III; ACY3 (gene name). Cat No: EXWM-4394. | |
| Native Human Cathepsin S | Cathepsin S is a lysosomal cysteine protease found primarily in the spleen and in lung macrophages. Its level is elevated in the brain tissue of those with Alzheimer's disease and Down syndrome. Cathepsin S may function in the processing of amyloid precursor protein to amyloid beta peptides. Applications: Cathepsin s from human spleen has been used in a study to assess the sequence identification, tissue distribution and polymorphism of the porcine cathepsin d (ctsd) gene. cathepsin s from human spleen has also been used in a study to investigate a new promising camptothecin analogue-polysaccharide conjugate. Group: Enzymes. Synonyms: CTSS; cathepsin S; EC 3.4.22.27; FLJ50259; MGC3886. Enzyme Commission Number: EC 3.4.22.27. CTSS. Storage: -70°C. Form: lyophilized powder. Lyophilized from 100 mM sodium acetate, pH 5.5, and 1 mM EDTA. Source: Human spleen. Species: Human. CTSS; cathepsin S; EC 3.4.22.27; FLJ50259; MGC3886. Cat No: NATE-0178. | |
| Native Rabbit Protein Phosphatase 1C | Protein Phosphatase 1 is a growth factor stimulated, divalent cation-independent serine/threonine protein phosphatase involved in regulating numerous cellular processes such as glycogen metabolism, mitosis, and meiosis. Protein phosphatase 1c (pp1c) is expressed in the dendrites of retinal bipolar cells where it was found to bind to group i metabotropic glutamate receptors indicating a function for pp1c in glutamatergic signal transduction. >90% (sds-page), buffered aqueous glycerol solution. Applications: Protein phosphatase-1c has been used in a study to investigate why two metabolites of microcystin-lr glutathione conjugate and microcystin-cysteine conjugate, as well as microcystin-rr are less toxic than microcystin-lr. Group: Enzymes. Synonyms: Protein Phosphatase 1C; PP1C. Purity: >90% (SDS-PAGE). Protein Phosphatase. Activity: > 1500 units/mg protein. Stability: -70°C. Form: buffered aqueous glycerol solution. Source: Rabbit muscle. Species: Rabbit. Protein Phosphatase 1C; PP1C. Cat No: NATE-0615. | |
| Nε-Trifluoroacetyl-L-lysine | . Uses: A cysteine conjugate metabolite adduct formation with specific mitochondrial proteins using antibodies raised against halothane metabolite adducts. Synonyms: L-Lys(Tfa)-OH. Grades: ≥ 99% (Assay). CAS No. 10009-20-8. Molecular formula: C8H13N2O3F3. Mole weight: 242. | |
| SPDP | SPDP (SPDP Crosslinker) is a short-chain crosslinker for amine-to-sulfhydryl conjugation via NHS-ester and pyridyldithiol reactive groups that form cleavable (reducible) disulfide bonds with cysteine sulfhydryls. It is a glutathione cleavable ADC linker used for the antibody-drug conjugates (ADCs) [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SPDP Crosslinker; Py-ds-Prp-OSu. CAS No. 68181-17-9. Pack Sizes: 25 mg; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-100216. | |
| Sulfo-N-succinimidyl 4-maleimidobutyrate sodium salt | Sulfo-N-succinimidyl 4-maleimidobutyrate, a water-soluble and heterobifunctional cross-linking reagent, is used to conjugate cysteine-containing peptides to carrier proteins or surfaces. Synonyms: Sulfo-GMBS sodium salt; Sodium 1-((4-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)butanoyl)oxy)-2,5-dioxopyrrolidine-3-sulfonate; 1-[4-(N-Maleimideyl)butyryloxy]-2,5-dioxopyrrolidine-3-sulfonic acid sodium salt; 3-Pyrrolidinesulfonic acid, 1-[4-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)-1-oxobutoxy]-2,5-dioxo-, sodium salt (1:1). Grades: ≥90%. CAS No. 185332-92-7. Molecular formula: C12H11N2NaO9S. Mole weight: 382.28. | |
| TAT (47-57) GGG-Cys(Npys) | It corresponds to the protein transduction domain of the TAT protein and is synthesized with an activated cysteine residue C(Npys), where Npys is 3-Nitro-2-pyridinesulfenyl group and is used for activating S of cysteine and for rapid reaction when a thiol group is introduced. The N-terminus is rendered free for applications requiring certain conjugation reactions with a free N-terminal end, and a linker GGG is placed at the C-terminal end, and the peptide has been synthesized with the C(Npys) group. This kind of modification has been used to render this peptide as a cell penetrating and carrier peptide applicable in conjugation studies. Synonyms: H-Tyr-Gly-Arg-Lys-Lys-Arg-Arg-Gln-Arg-Arg-Arg-Gly-Gly-Gly-Cys(Npys)-NH2. Grades: ≥95%. Molecular formula: C78H135N39O19S2. Mole weight: 1987.29. | |
| Tau Peptide (294-305) (human) | Tau 294-305, an anti-tau vaccine, conjugates to KLH via an N-terminal cysteine. Tau Peptide (294-305) (human) may prevent the formation of beta/beta-helix structure of protofilaments, including residues 306-378. Synonyms: Microtubule-Associated Protein Tau (610-621) (human); H-Lys-Asp-Asn-Ile-Lys-His-Val-Pro-Gly-Gly-Gly-Ser-OH; L-Lysyl-L-α-aspartyl-L-asparaginyl-L-isoleucyl-L-lysyl-L-histidyl-L-valyl-L-prolylglycylglycylglycyl-L-serine. Grades: ≥95%. CAS No. 1428135-29-8. Molecular formula: C51H85N17O17. Mole weight: 1208.32. | |
| Desacetyl acetaminophen glutathione | Desacetyl Acetaminophen Glutathione is a hepatic metabolite of Acetaminophen, which is a selective COX-2 inhibitor used as an antipyretic, analgesic, and anti-inflammatory agent. Uses: The hepatic metabolite of p-aminophenol. the aminophenol glutathione s-conjugates formed induce p-aminophenol nephrotoxicity by a pathway dependent on γ-glutamyl transpeptidase. Synonyms: N-[S-(5-Amino-2-hydroxyphenyl)-N-L-γ-glutamyl-L-cysteinyl]glycine; Glycine, N-[S-(5-amino-2-hydroxyphenyl)-N-L-γ-glutamyl-L-cysteinyl]-. Grades: 95%. CAS No. 129762-76-1. Molecular formula: C16H22N4O7S. Mole weight: 414.43. | |
| Desacetyl Acetaminophen Glutathione. | The hepatic metabolite of p-Aminophenol. The aminophenol glutathione S-conjugates formed induce p-Aminophenol nephrotoxicity by a pathway dependent on γ-glutamyl transpeptidase. Group: Biochemicals. Alternative Names: N-[S-(5-Amino-2-hydroxyphenyl)-N-L-γ-glutamyl-L-cysteinyl]glycine. Grades: Highly Purified. CAS No. 129762-76-1. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Integrin Binding Peptide | Integrin Binding Peptide is a peptide containing the cell adhesion sequence RGDSP, which is easily conjugated to carriers via Npys or maleimide chemistry. Synonyms: Ac-Gly-Cys-Gly-Tyr-Gly-Arg-Gly-Asp-Ser-Pro-Gly-NH2; N-acetyl-glycyl-L-cysteinyl-glycyl-L-tyrosyl-glycyl-L-arginyl-glycyl-L-alpha-aspartyl-L-seryl-L-prolyl-glycinamide; Glycinamide, N-acetylglycyl-L-cysteinylglycyl-L-tyrosylglycyl-L-arginylglycyl-L-α-aspartyl-L-seryl-L-prolyl-. Grades: ≥95%. CAS No. 278792-07-7. Molecular formula: C42H63N15O16S. Mole weight: 1066.12. | |
| Leukotriene C4 | Leukotriene C4 is a cysteinyl leukotriene produced by the LTC4 synthase catalyzed conjugation of glutathione to LTA4. LTC4 acts as an agonist of smooth muscle contraction. LTC4-induced bronchoconstriction and enhanced vascular permeability contribute to the pathogenesis of asthma and acute allergic hypersensitivity. Synonyms: LTC4; 5S,6R-Ltc(sub 4); 6R-(((R)-2-((S)-4-amino-4-carboxybutanamido)-3-((carboxymethyl)amino)-3-oxopropyl)thio)-5S-hydroxyicosa-7E,9E,11Z,14Z-eicosatetraenoic acid. Grades: ≥97%. CAS No. 72025-60-6. Molecular formula: C30H47N3O9S. Mole weight: 625.78. | |
| Leukotriene C4 methyl ester | Leukotriene C4 is a cysteinyl leukotriene produced by the LTC4 synthase catalyzed conjugation of glutathione to LTA4. LTC4 acts as an agonist of smooth muscle contraction. LTC4-induced bronchoconstriction and enhanced vascular permeability contribute to the pathogenesis of asthma and acute allergic hypersensitivity. Synonyms: LTC4 methyl ester; Leukotriene C4 monomethyl ester. Grades: ≥97%. CAS No. 73958-10-8. Molecular formula: C31H49N3O9S. Mole weight: 639.8. | |
| Pam2CSK4 Biotin | Pam2CSK4 Biotin is the biotinylated Pam2CSK4. Pam2CSK4, a synthetic diacylated lipopeptide (LP), is a toll-like receptor 2/6 (TLR2/6) agonist, and induces TNF-α production in human mononuclear cells. Synonyms: Pam2CSK4 (Biotin Conjugate); N2-S-((R)-2,3-bis(palmitoyloxy)propyl)-L-cysteinyl-L-seryl-L-lysyl-L-lysyl-L-lysyl-N6-(6-(6-(5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamido)hexanamido)hexanoyl)-L-lysine. Grades: ≥95%. CAS No. 1883545-45-6. Molecular formula: C87H162N14O16S2. Mole weight: 1724.44. | |
| RGD-targeted Proapoptotic Peptide | RGD-targeted Proapoptotic Peptide is RGD-4C conjugated to a full D proapoptotic peptide. Synonyms: RGD-4C-GG-(klaklak)2-NH2; H-Ala-Cys-Asp-Cys-Arg-Gly-Asp-Cys-Phe-Cys-Gly-Gly-D-Lys-D-Leu-D-Ala-D-Lys-D-Leu-D-Ala-D-Lys-D-Lys-D-Leu-D-Ala-D-Lys-D-Leu-D-Ala-D-Lys-OH (Disulfide bridge: Cys2-Cys10, Cys4-Cys8); D-Lysine, L-alanyl-L-cysteinyl-L-α-aspartyl-L-cysteinyl-L-arginylglycyl-L-α-aspartyl-L-cysteinyl-L-phenylalanyl-L-cysteinylglycylglycyl-D-lysyl-D-leucyl-L-alanyl-D-lysyl-D-leucyl-D-alanyl-D-lysyl-D-lysyl-D-leucyl-D-alanyl-D-lysyl-D-leucyl-D-alanyl-, cyclic(2?10),(4?8)-bis(disulfide). Grades: ≥95%. CAS No. 2243207-09-0. Molecular formula: C116H199N35O31S4. Mole weight: 2708.34. | |
| S- (2-Hydroxypropyl) glutathione | A biliary glutamyl cysteinyl glycine (GSH) conjugate metabolite of 1,2-dibromo-3-chloropropane (DBCP). Group: Biochemicals. Alternative Names: L-γ-Glutamyl-S-(2-hydroxypropyl)-L-cysteinylgycine; N-[N-L-γ-glutamyl-S-(2-hydroxypropyl)-L-cysteinyl]glycine. Grades: Highly Purified. CAS No. 85933-29-5. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| S- (2-Hydroxypropyl) glutathione-d6 | A labeled biliary glutamyl cysteinyl glycine (GSH) conjugate metabolite of 1,2-dibromo-3-chloropropane (DBCP). Group: Biochemicals. Alternative Names: L-γ-Glutamyl-S-(2-hydroxypropyl)-L-cysteinylgycine-d6; N-[N-L-γ-glutamyl-S-(2-hydroxypropyl)-L-cysteinyl]glycine-d6. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| S, S'-Ethylenebis (glutathione) | S, S'-Ethylenebis (glutathione) is a haloethane-glutathione conjugate formed via GSH transferases. S, S'-Ethylenebis (glutathione) formation is used to study the polymorphism in glutathione conjugation activity of human erythrocytes towards ethylene dibromide. Group: Biochemicals. Alternative Names: 2,2'-(1,2-Ethanediyl)bis[L-γ-glutamyl-L-cysteinylglycine. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
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