Silver(1 ) diethyldithiocarbamate

By Targets:	Bacterial (2) Biochemical Assay Reagents (2) Carbonic Anhydrase (1) Histone Methyltransferase (1) HIV (2) Interleukin Related (1) Isotope-Labeled Compounds (1) Melanocortin Receptor (2) Vasopressin Receptor (3)
By Research Areas:	Cancer (3) Cardiovascular Disease (1) Infection (5) Inflammation/Immunology (1) Metabolic Disease (1) Neurological Disease (3)

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-W034674

**Silver diethyldithiocarbamate** Silver(1+) diethyldithiocarbamate	Biochemical Assay Reagents	Others
Silver diethyldithiocarbamate (SDDC) is an organic compound consisting of silver ions complexed with the ligand diethyldithiocarbamate. SDDC is mainly used as a reagent in analytical chemistry to detect the presence of copper, iron and other heavy metals in various materials. It acts as a chelating agent, binding to metal ions and forming stable complexes that can be easily analyzed using techniques such as UV-Vis spectroscopy.

HY-B1637

Ditiocarb sodium 3 Publications Verification Sodium diethyldithiocarbamate	HIV	Infection
Ditiocarb sodium (Sodium diethyldithiocarbamate) is an accelerator of the rate of copper cementation. Sodium diethyldithiocarbamate reduces the incidence of HIV infection, and also enhances adjuvant immunoresearch of high risk breast cancer ^[1] .

HY-W111581

Copper(II) diethyldithiocarbamate Diethyldithiocarbamic acid copper salt	Others	Cancer
Copper(II) diethyldithiocarbamate has anticancer activity. Copper(II) diethyldithiocarbamate can be synthesized from monovalent copper-cysteamine and disulfiram ^[1].

HY-143850S

Methyl diethyldithiocarbamate-d3

Isotope-Labeled Compounds Others

Methyl diethyldithiocarbamate-d₃ is the deuterium labeled Methyl diethyldithiocarbamate[1].

*Methyl diethyldithiocarbamate-d3*	Isotope-Labeled Compounds	Others
Methyl diethyldithiocarbamate-d₃ is the deuterium labeled Methyl diethyldithiocarbamate[1].

HY-B1637S

Ditiocarb-d10 sodium	HIV	Infection
Ditiocarb-d₁₀ (sodium) is the deuterium labeled Ditiocarb sodium[1]. Ditiocarb sodium (Sodium diethyldithiocarbamate) is an accelerator of the rate of copper cementation. Sodium diethyldithiocarbamate reduces the incidence of HIV infection[2][3].

HY-P9923A

Benralizumab (anti-IL5RA ) MEDI-563 (anti-IL5RA ); BIW-8405 (anti-IL5RA )	Interleukin Related	Inflammation/Immunology
Benralizumab (anti-IL5RA ) (MEDI-563 (anti-IL5RA ); BIW-8405 (anti-IL5RA )) is an interleukin-5 receptor α (IL-5Rα)-directed cytolytic monoclonal antibody that induces direct, rapid and nearly complete depletion of eosinophils via enhanced antibody-dependent cell-mediated cytotoxicity. Benralizumab can be used for severe eosinophilic asthma study ^[1] .

HY-101505

Zinc dethyldithiocarbamate Ethyl ziram	Biochemical Assay Reagents	Others
Zinc Diethyldithiocarbamate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

HY-100869B

MM-589 (racemic mixture ) (TFA)	Histone Methyltransferase	Cancer
MM-589 (racemic mixture) TFA, is a racemic mixture of MM-589 TFA (HY-100869A). MM-589 TFA is a potent inhibitor of WD repeat domain 5 (WDR5) and mixed lineage leukemia (MLL) protein-protein interaction. MM-589 binds to WDR5 with an IC₅₀ of 0.90 nM and inhibits the MLL H3K4 methyltransferase activity with an IC₅₀ of 12.7 nM ^[1].

HY-N7057

Nonanoic acid Pelargonic acid; Pelargonic acid (n-Nonanoic acid, C9 )	Bacterial	Infection
Nonanoic acid is a naturally-occurring saturated fatty acid with nine carbon atoms. Nonanoic acid significantly reduces bacterial translocation, enhances antibacterial activity, and remarkably increases the secretion of porcine β-defensins 1 (pBD-1) and pBD-2 ^[1].

HY-N7057S3

Nonanoic acid-d2 Pelargonic acid-d₂; Pelargonic acid-d2 (n-Nonanoic acid, C9 )	Bacterial	Infection
Nonanoic acid-d₂ is the deuterium labeled Nonanoic acid[1]. Nonanoic acid is a naturally-occurring saturated fatty acid with nine carbon atoms. Nonanoic acid significantly reduces bacterial translocation, enhances antibacterial activity, and remarkably increases the secretion of porcine β-defensins 1 (pBD-1) and pBD-2[2].

HY-P1726A

MSG606 TFA	Melanocortin Receptor
MSG606 TFA is a potent human MC1 receptor antagonist (IC₅₀=17 nM). MSG606 TFA also partial agonist at human MC3 and MC5 receptors (EC₅₀ values are 59 and 1300 nM, respectively). MSG606 TFA exhibits binding affinity for A375 melanoma cells in vitro. MSG606 TFA reverses the induced hyperalgesia in female mice, with no effect in male mice.

HY-P1726

MSG606

Melanocortin Receptor Neurological Disease

MSG606 is a selective MC1R (melanocortin 1 receptor) antagonist and can be used for the research of neuroprotective effects ^[1].

MSG606	Melanocortin Receptor	Neurological Disease
MSG606 is a selective *MC1R* (melanocortin 1 receptor) antagonist and can be used for the research of neuroprotective effects ^[1].

HY-P3066

SKF 100398 d(CH2)5Tyr(Et)VAVP	Vasopressin Receptor	Metabolic Disease
SKF 100398 (d(CH2)5Tyr(Et)VAVP), an arginine vasopressin (AVP) analogue, is a specific antagonist of the antidiuretic effect of exogenous and endogenous AVP ^[1].

HY-157135

hCAIX-IN-19	Carbonic Anhydrase	Cancer
hCAIX-IN-19 is a sulfonamides inhibitor against hCA IX with an inhibition constant (K_I) of 6.2 nM and show good selectivity over hCA I (hCA I/ hCA IX = 117) ^[1].

HY-P0041

F992

Vasopressin Receptor Neurological Disease

F992 is an antidiuretic peptide and vasopressin (antidiuretic hormone) analogue ^[1].
HY-P0041A

F992 TFA

Vasopressin Receptor Neurological Disease

F992 TFA is an antidiuretic peptide and vasopressin (antidiuretic hormone) analogue ^[1].

F992	Vasopressin Receptor	Neurological Disease
F992 is an antidiuretic peptide and vasopressin (antidiuretic hormone) analogue ^[1].

F992 TFA	Vasopressin Receptor	Neurological Disease
F992 TFA is an antidiuretic peptide and vasopressin (antidiuretic hormone) analogue ^[1].

Cat. No.	Product Name	Type

HY-W034674

**Silver diethyldithiocarbamate** Silver(1+) diethyldithiocarbamate	Biochemical Assay Reagents
Silver diethyldithiocarbamate (SDDC) is an organic compound consisting of silver ions complexed with the ligand diethyldithiocarbamate. SDDC is mainly used as a reagent in analytical chemistry to detect the presence of copper, iron and other heavy metals in various materials. It acts as a chelating agent, binding to metal ions and forming stable complexes that can be easily analyzed using techniques such as UV-Vis spectroscopy.

Silver diethyldithiocarbamate

Silver(1+) diethyldithiocarbamate

Biochemical Assay Reagents

Silver diethyldithiocarbamate (SDDC) is an organic compound consisting of silver ions complexed with the ligand diethyldithiocarbamate. SDDC is mainly used as a reagent in analytical chemistry to detect the presence of copper, iron and other heavy metals in various materials. It acts as a chelating agent, binding to metal ions and forming stable complexes that can be easily analyzed using techniques such as UV-Vis spectroscopy.

HY-101505

Zinc dethyldithiocarbamate Ethyl ziram	Biochemical Assay Reagents
Zinc Diethyldithiocarbamate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

Cat. No.	Product Name	Target	Research Area

HY-P3066

SKF 100398 d(CH2)5Tyr(Et)VAVP	Vasopressin Receptor	Metabolic Disease
SKF 100398 (d(CH2)5Tyr(Et)VAVP), an arginine vasopressin (AVP) analogue, is a specific antagonist of the antidiuretic effect of exogenous and endogenous AVP ^[1].

HY-P4756

*N-(2-Carbamoyl-ethyl)-Val-Leu-anilide*	Peptides	Others
N-(2-Carbamoyl-ethyl)-Val-Leu-anilide is a polypeptide that can be found by peptide screening. Peptide screening is a research tool that pools active peptides primarily by immunoassay. Peptide screening can be used for protein interaction, functional analysis, epitope screening, especially in the field of agent research and development ^[1].

HY-P2331

Actagardin Antibiotic A 3802-IV-3; Gardimycin	Peptides	Infection
Actagardin is a tetracyclic lantibiotic produced by several species of Actinoplanes. It is composed of macrocyclic rings formed by thioether bridges. Actagardin preferably targets Gram-positive bacteria, inhibiting the synthesis of peptidoglycan.

HY-P10014

Bibapcitide

Peptides Cardiovascular Disease

Bibapcitide, a 26 amino acid, inhibits thrombosis ^[1].

Bibapcitide	Peptides	Cardiovascular Disease
Bibapcitide, a 26 amino acid, inhibits thrombosis ^[1].

HY-P1726A

MSG606 TFA	Melanocortin Receptor
MSG606 TFA is a potent human MC1 receptor antagonist (IC₅₀=17 nM). MSG606 TFA also partial agonist at human MC3 and MC5 receptors (EC₅₀ values are 59 and 1300 nM, respectively). MSG606 TFA exhibits binding affinity for A375 melanoma cells in vitro. MSG606 TFA reverses the induced hyperalgesia in female mice, with no effect in male mice.

HY-P0041

F992

Vasopressin Receptor Neurological Disease

F992 is an antidiuretic peptide and vasopressin (antidiuretic hormone) analogue ^[1].
HY-P0041A

F992 TFA

Vasopressin Receptor Neurological Disease

F992 TFA is an antidiuretic peptide and vasopressin (antidiuretic hormone) analogue ^[1].

F992	Vasopressin Receptor	Neurological Disease
F992 is an antidiuretic peptide and vasopressin (antidiuretic hormone) analogue ^[1].

F992 TFA	Vasopressin Receptor	Neurological Disease
F992 TFA is an antidiuretic peptide and vasopressin (antidiuretic hormone) analogue ^[1].

Cat. No.	Product Name	Target	Research Area

HY-P9923A

Benralizumab (anti-IL5RA ) MEDI-563 (anti-IL5RA ); BIW-8405 (anti-IL5RA )	Interleukin Related	Inflammation/Immunology
Benralizumab (anti-IL5RA ) (MEDI-563 (anti-IL5RA ); BIW-8405 (anti-IL5RA )) is an interleukin-5 receptor α (IL-5Rα)-directed cytolytic monoclonal antibody that induces direct, rapid and nearly complete depletion of eosinophils via enhanced antibody-dependent cell-mediated cytotoxicity. Benralizumab can be used for severe eosinophilic asthma study ^[1] .

Cat. No.	Product Name	Category	Target	Chemical Structure

HY-N7057

Nonanoic acid Pelargonic acid; Pelargonic acid (n-Nonanoic acid, C9 )	Infection Malvaceae Microorganisms Classification of Application Fields Hibiscus syriacus Ketones, Aldehydes, Acids Source classification Plants Disease Research Fields Biological Pesticide Research Agricultural Research	Bacterial
Nonanoic acid is a naturally-occurring saturated fatty acid with nine carbon atoms. Nonanoic acid significantly reduces bacterial translocation, enhances antibacterial activity, and remarkably increases the secretion of porcine β-defensins 1 (pBD-1) and pBD-2 ^[1].

Species:	Virus (1) Human (1)
Tag:	His (1) Fc (1)
Source:	HEK293 (2)

Cat. No.	Compare	Product Name	Species	Source

HY-P70004

	CD36 Protein, Human (HEK293, Fc ) rHuPlatelet glycoprotein 4/CD36, Fc; Fatty acid translocase; Glycoprotein IIIb; FATCHDS7; Leukocyte differentiation antigen CD36; PAS IV; Platelet collagen receptor; SCARB3; Thrombospondin receptor; CD36	Human	HEK293
	CD36 is a multifunctional glycoprotein that serves as a receptor for a variety of ligands, including thrombospondin and oxidized low-density lipoprotein. Ligand induces CD36 clusters, initiating signal transduction and internalization. CD36 Protein, Human (HEK293, Fc ) is the recombinant human-derived CD36 protein, expressed by HEK293 , with C-hFc labeled tag. The total length of CD36 Protein, Human (HEK293, Fc ) is 410 a.a., with molecular weight of 90-130 kDa.

HY-P74933

	HA1/Hemagglutinin Protein, H5N8 (EPI544756, HEK293, His) Influenza A H5N8 (A/turkey/Germany-MV/R2472/2014 ) Hemagglutinin / HA1 Protein (His)	Virus	HEK293
	The hemagglutinin (HA) protein attaches viral particles to host cells by binding to sialic acid-containing receptors and induces viral particle internalization through clathrin-dependent endocytosis. HA also promotes an alternative clathrin- and caveolin-independent pathway for some virions. HA1/Hemagglutinin Protein, H5N8 (EPI544756, HEK293, His) is the recombinant Virus-derived HA1/Hemagglutinin protein, expressed by HEK293 , with C-His labeled tag. The total length of HA1/Hemagglutinin Protein, H5N8 (EPI544756, HEK293, His) is 345 a.a., with molecular weight of ~38.8 kDa.


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Cat. No.	Product Name	Chemical Structure

HY-N7057S3

Nonanoic acid-d2
Nonanoic acid-d₂ is the deuterium labeled Nonanoic acid[1]. Nonanoic acid is a naturally-occurring saturated fatty acid with nine carbon atoms. Nonanoic acid significantly reduces bacterial translocation, enhances antibacterial activity, and remarkably increases the secretion of porcine β-defensins 1 (pBD-1) and pBD-2[2].

HY-143850S

Methyl diethyldithiocarbamate-d3

Methyl diethyldithiocarbamate-d₃ is the deuterium labeled Methyl diethyldithiocarbamate[1].

*Methyl diethyldithiocarbamate-d3*
Methyl diethyldithiocarbamate-d₃ is the deuterium labeled Methyl diethyldithiocarbamate[1].

HY-B1637S

Ditiocarb-d10 sodium
Ditiocarb-d₁₀ (sodium) is the deuterium labeled Ditiocarb sodium[1]. Ditiocarb sodium (Sodium diethyldithiocarbamate) is an accelerator of the rate of copper cementation. Sodium diethyldithiocarbamate reduces the incidence of HIV infection[2][3].

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Inhibitors & Agonists

Biochemical Assay Reagents

Peptides

Inhibitory Antibodies

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Recombinant Proteins

Isotope-Labeled Compounds

Silver(1 ) diethyldithiocarbamate

Inhibitors & Agonists

Biochemical Assay Reagents

Peptides

Inhibitory Antibodies

NaturalProducts

Recombinant Proteins

Isotope-Labeled Compounds

Natural
Products