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Cefalexin hydrate-d<sub>5</sub>

" in MedChemExpress (MCE) Product Catalog:

3869

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1

Screening Libraries

19

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7

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1

Inhibitory Antibodies

23

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Products

11

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3752

Isotope-Labeled Compounds

4

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Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-B0200S
    Cephalexin-d5

    Cefalexin-d<sub>5sub>; Cephacillin-d<sub>5sub>

    		 Antibiotic Bacterial Infection
    Cephalexin-d5 is deuterium labeled Cephalexin. Cephalexin (Cefalexin; Cephacillin) is a potent, orally active and the first-generation?cephalosporin antibiotic. Cephalexin kills?gram-positive?and some?gram-negative bacteria?by disrupting the growth of the bacterial cell wall. Cephalexin monohydrate is used for the research of?pneumonia,?strep throat, and bacterial endocarditis, et al .
    Cephalexin-d5
  • HY-B0200A
    Cephalexin hydrochloride
    5+ Cited Publications

    Cefalexin hydrochloride; Cephacillin hydrochloride

    		 Penicillin-binding protein (PBP) Bacterial Antibiotic Infection Cancer
    Cephalexin (Cefalexin) hydrochloride is a potent, orally active new semisynthetic cephalosporin antibiotic with a broad antibacterial spectrum. Cephalexin (Cefalexin) hydrochloride has antibacterial activity against a wide variety of gram-positive and gram-negative bacteria. Cephalexin (Cefalexin) hydrochloride targets penicillin-binding proteins (PBPs) to inhibit bacterial cell wall assembly. Cephalexin (Cefalexin) hydrochloride is used for the research of pneumonia, strep throat, and bacterial endocarditis, et al .
    Cephalexin hydrochloride
  • HY-B0200B
    Cephalexin monohydrate
    5+ Cited Publications

    Cefalexin hydrate; Cephacillin hydrate

    		 Penicillin-binding protein (PBP) Antibiotic Bacterial Infection Cancer
    Cephalexin (Cefalexin) monohydrate is a potent, orally active new semisynthetic cephalosporin antibiotic with a broad antibacterial spectrum. Cephalexin (Cefalexin) monohydrate has antibacterial activity against a wide variety of gram-positive and gram-negative bacteria. Cephalexin (Cefalexin) monohydrate targets penicillin-binding proteins (PBPs) to inhibit bacterial cell wall assembly. Cephalexin (Cefalexin) monohydrate is used for the research of pneumonia, strep throat, and bacterial endocarditis, et al .
    Cephalexin monohydrate
  • HY-B0200BS
    Cephalexin-d5 monohydrate

    Cefalexin hydrate-d<sub>5sub>; Cephacillin hydrate-d<sub>5sub>

    		 Isotope-Labeled Compounds Antibiotic Bacterial Infection
    Cephalexin-d5 (monohydrate) is the deuterium labeled Cephalexin monohydrate. Cephalexin monohydrate is a potent, orally active and the first-generation?cephalosporin antibiotic. Cephalexin monohydrate kills?gram-positive?and some?gram-negative bacteria?by disrupting the growth of the bacterial cell wall. Cephalexin monohydrate is used for the research of?pneumonia,?strep throat, and bacterial endocarditis, et al .
    Cephalexin-d5 monohydrate
  • HY-10844S1
    Pretomanid-d5

    PA-824-d<sub>5sub>; (S)-PA 824-d<sub>5sub>

    		 Antibiotic Bacterial Isotope-Labeled Compounds Infection Cancer
    Pretomanid-d5 is deuterated labeled Pretomanid (HY-10844). Pretomanid (PA-824) is an antibiotic used for the research of multi-drug-resistant tuberculosis affecting the lungs. Pretomanid exhibits a sub-micromolar MIC against M. tuberculosis (MTB). The MIC values of PA-824 against a panel of MTB pan-sensitive and Rifampin mono-resistant clinical isolates range from 0.015 to 0.25 μg/mL.
    Pretomanid-d5
  • HY-RS13999
    SUB1 Human Pre-designed siRNA Set A

    		Small Interfering RNA (siRNA) Others

    SUB1 Human Pre-designed siRNA Set A contains three designed siRNAs for SUB1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    SUB1 Human Pre-designed siRNA Set A
    SUB1 Human Pre-designed siRNA Set A
  • HY-RS18793
    Sub1 Mouse Pre-designed siRNA Set A

    		Small Interfering RNA (siRNA) Others

    Sub1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Sub1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Sub1 Mouse Pre-designed siRNA Set A
    Sub1 Mouse Pre-designed siRNA Set A
  • HY-RS25282
    Sub1 Rat Pre-designed siRNA Set A

    		Small Interfering RNA (siRNA) Others

    Sub1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Sub1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Sub1 Rat Pre-designed siRNA Set A
    Sub1 Rat Pre-designed siRNA Set A
  • HY-146227
    DNA topoisomerase II inhibitor 1

    		Topoisomerase Apoptosis Cancer
    DNA topoisomerase II inhibitor 1 (compound 8ed) is a potent DNA topoisomerase II inhibitor. DNA topoisomerase II inhibitor 1 shows anti-proliferative activity. DNA topoisomerase II inhibitor 1 induces apoptosis and cell cycle arrest at sub G1 phase .
    DNA topoisomerase II inhibitor 1
  • HY-B0200C
    Cephalexin hydrochloride monohydrate

    Cefalexin hydrochloride monohydrate; Cephacillin hydrochloride monohydrate

    		 Penicillin-binding protein (PBP) Antibiotic Bacterial Infection Cancer
    Cephalexin (Cefalexin) hydrochloride monohydrate is a potent, orally active new semisynthetic cephalosporin antibiotic with a broad antibacterial spectrum. Cephalexin (Cefalexin) hydrochloride monohydrate has antibacterial activity against a wide variety of gram-positive and gram-negative bacteria. Cephalexin (Cefalexin) hydrochloride monohydrate targets penicillin-binding proteins (PBPs) to inhibit bacterial cell wall assembly. Cephalexin (Cefalexin) hydrochloride monohydrate is used for the research of pneumonia, strep throat, and bacterial endocarditis, et al .
    Cephalexin hydrochloride monohydrate
  • HY-B0200AR
    Cephalexin hydrochloride (Standard)

    Cefalexin hydrochloride (Standard); Cephacillin hydrochloride (Standard)

    		 Penicillin-binding protein (PBP) Bacterial Antibiotic Infection Cancer
    Cephalexin (hydrochloride) (Standard) is the analytical standard of Cephalexin (hydrochloride). This product is intended for research and analytical applications. Cephalexin (Cefalexin) hydrochloride is a potent, orally active new semisynthetic cephalosporin antibiotic with a broad antibacterial spectrum. Cephalexin (Cefalexin) hydrochloride has antibacterial activity against a wide variety of gram-positive and gram-negative bacteria. Cephalexin (Cefalexin) hydrochloride targets penicillin-binding proteins (PBPs) to inhibit bacterial cell wall assembly. Cephalexin (Cefalexin) hydrochloride is used for the research of pneumonia, strep throat, and bacterial endocarditis, et al[1][2].
    Cephalexin hydrochloride (Standard)
  • HY-P10215
    Ac-{Cpg}-Thr-Ala-{Ala(CO)}-Asp-{Cpg}-NH2

    		Parasite Infection
    Ac-{Cpg}-Thr-Ala-{Ala(CO)}-Asp-{Cpg}-NH2 (compound 40) is a potent Plasmodium subtilisin-like protease 1 (SUB1) inhibitor. SUB1-IN-1 shows IC50 values of 12 nM and 10 nM against P. vivax and P. falciparum SUB1 (Pv- and PfSUB1), respectively .
    Ac-{Cpg}-Thr-Ala-{Ala(CO)}-Asp-{Cpg}-NH2
  • HY-B0200
    Cephalexin
    5+ Cited Publications

    Cefalexin; Cephacillin

    		 Penicillin-binding protein (PBP) Antibiotic Bacterial Infection Cancer
    Cephalexin (Cefalexin) is a potent, orally active semisynthetic cephalosporin antibiotic with a broad antibacterial spectrum. Cephalexin has antibacterial activity against a wide variety of gram-positive and gram-negative bacteria. Cephalexin targets penicillin-binding proteins (PBPs) to inhibit bacterial cell wall assembly. Cephalexin is used for the research of pneumonia, strep throat, and bacterial endocarditis, et al .
    Cephalexin
  • HY-W700392
    IMPDH-IN-2

    		IMPDH Cancer
    IMPDH-IN-2 (compound 2) is an inhibitor of inosine monophosphate dehydrogenase (IMPDH) with IC50 for IMPDH I and IMPDH II >Values are 0.15 and 0.17 μM, respectively. IMPDH-IN-2 has antitumor activity .
    IMPDH-IN-2
  • HY-14198S
    Selegiline-d5

    Deprenyl-d<sub>5sub>; (-)-Selegiline-d<sub>5sub>; (-)-Deprenyl-d<sub>5sub>

    		 Isotope-Labeled Compounds Monoamine Oxidase Neurological Disease
    Selegiline-d5 (Deprenyl-d5) is deuterium labeled Selegiline. Selegiline (Deprenyl) is a potent, selective and irreversible inhibitor of MAO-B, with an IC50 of 51 nM. Selegiline exhibits 450-flod selectivity for MAO-B over MAO-A (IC50=23 μM). Selegiline can be used for the research of Parkinson's disease, Alzheimer's disease and major depressive disorder .
    Selegiline-d5
  • HY-W012481S
    Nirvanol-d5

    Ethylphenylhydantoin-d<sub>5sub>; Phenylethyihydantoin-d<sub>5sub>; Desmethylmephenytoin-d<sub>5sub>

    		 Isotope-Labeled Compounds Drug Metabolite Neurological Disease
    Nirvanol-d5 (Ethylphenylhydantoin-d5) is deuterium labeled Nirvanol (HY-W012481) . Nirvanol (Ethylphenylhydantoin) is a metabolite of Mephenytoin (HY-B1184) that exerts anticonvulsant effects in the maximal electroshock (M.E.S.) seizure model in mice. Nirvanol shows potential for research in epilepsy-related neurological disorders .
    Nirvanol-d5
  • HY-14199S
    Selegiline-d5 hydrochloride

    Deprenyl-d<sub>5sub> hydrochloride; (-)-Selegiline-d<sub>5sub> hydrochloride; (-)-Deprenyl-d<sub>5sub> hydrochloride

    		 Isotope-Labeled Compounds Monoamine Oxidase Neurological Disease
    Selegiline-d5 (hydrochloride) (Deprenyl-d5 (hydrochloride)) is deuterium labeled Selegiline (hydrochloride). Selegiline (Deprenyl) hydrochloride is a potent, selective and irreversible inhibitor of MAO-B, with an IC50 of 51 nM. Selegiline hydrochloride exhibits 450-flod selectivity for MAO-B over MAO-A (IC50=23 μM). Selegiline hydrochloride can be used for the research of Parkinson's disease, Alzheimer's disease and major depressive disorder .
    Selegiline-d5 hydrochloride
  • HY-U00315S
    Gidazepam-d5

    Gidasepam-d<sub>5sub>; Hidazepam-d<sub>5sub>; Hydazepam-d<sub>5sub>

    		 GABA Receptor Neurological Disease
    Gidazepam-d5 is a deuterium labeled Gidazepam. Gidazepam is an agonist of GABA receptor channels (GABA RCs), and has anticonvulsant effect .
    Gidazepam-d5
  • HY-B0184S1
    Felbamate-d5

    Felbamyl-d<sub>5sub>; Felbatol-d<sub>5sub>; Taloxa-d<sub>5sub>

    		 iGluR Neurological Disease
    Felbamate-d5 is the deuterium labeled Felbamate . Felbamate (W-554) is a potent nonsedative anticonvulsant whose clinical effect may be related to the inhibition of N-methyl-D-aspartate (NMDA) .
    Felbamate-d5
  • HY-16560S
    Camptothecin-d5

    Campathecin-d<sub>5sub>; (S)-(+)-Camptothecin-d<sub>5sub>; CPT-d<sub>5sub>

    		 Isotope-Labeled Compounds Topoisomerase ADC Cytotoxin MicroRNA Influenza Virus Apoptosis Fungal Antibiotic Infection Cancer
    Camptothecin-d5 is the deuterium labeled Camptothecin. Camptothecin (CPT), a kind of alkaloid, is a DNA topoisomerase I (Topo I) inhibitor with an IC50 of 679 nM . Camptothecin (CPT) exhibits powerful antineoplastic activity against colorectal, breast, lung and ovarian cancers, modulates hypoxia-inducible factor-1α (HIF-1α) activity by changing microRNAs (miRNA) expression patterns in human cancer cells .
    Camptothecin-d5
  • HY-B0715S2
    Pentoxifylline-d5

    BL-191-d<sub>5sub>; PTX-d<sub>5sub>; Oxpentifylline-d<sub>5sub>

    		 Phosphodiesterase (PDE) Autophagy HIV Cardiovascular Disease Cancer
    Pentoxifylline-d5 is the deuterium labeled Pentoxifylline. Pentoxifylline (BL-191), a haemorheological agent, is an orally active non-selective phosphodiesterase (PDE) inhibitor, with immune modulation, anti-inflammatory, hemorheological, anti-fibrinolytic and anti-proliferation effects. Pentoxifylline can be used for the research of peripheral vascular disease, cerebrovascular disease and a number of other conditions involving a defective regional microcirculation .
    Pentoxifylline-d5
  • HY-107819S
    5α-Cholestan-3β-ol-d5

    Dihydrocholesterol-d<sub>5sub>; 5α-Cholestanol-d<sub>5sub>; NSC 18188-d<sub>5sub>

    		 Isotope-Labeled Compounds Endogenous Metabolite Others
    5α-Cholestan-3β-ol-d5 is the deuterium labeled 5α-Cholestan-3β-ol. 5α-Cholestan-3β-ol is a derivitized steroid compound .
    5α-Cholestan-3β-ol-d5
  • HY-158252S
    Tiagabine-d5 hydrochloride

    NO050328-d<sub>5sub> hydrochloride; NO328-d<sub>5sub> hydrochloride; TGB-d<sub>5sub> hydrochloride

    		 Isotope-Labeled Compounds GABA Receptor Neurological Disease
    Tiagabine-d5 (hydrochloride) is deuterium labeled Tiagabine (hydrochloride). Tiagabine hydrochloride is a potent and selective GABA reuptake inhibitor, used as an anticonvulsant agent, with IC50s of 67, 446 and 182 nM for [ 3H]GABA uptake in Synaptosomes, Neurons and Glia, respectively .
    Tiagabine-d5 hydrochloride
  • HY-144162S
    (Rac)-Selegiline-d5 hydrochloride

    (Rac)-Deprenyl-d<sub>5sub> hydrochloride; (±)-Selegiline-d<sub>5sub> hydrochloride; (±)-Deprenyl-d<sub>5sub> hydrochloride

    		 Isotope-Labeled Compounds Others
    (Rac)-Selegiline-d5 (hydrochloride) is the deuterium labeled (Rac)-Selegiline hydrochloride .
    (Rac)-Selegiline-d5 hydrochloride
  • HY-66005S5
    Acetaminophen-d5

    Paracetamol-d<sub>5sub>; 4-Acetamidophenol-d<sub>5sub>; 4'-Hydroxyacetanilide-d<sub>5sub>

    		 Isotope-Labeled Compounds Others
    Acetaminophen-d5 is deuterated-labeled Acetaminophen.
    Acetaminophen-d5
  • HY-109044S
    Tapinarof-d5

    WBI-1001-d<sub>5sub>; Benvitimod-d<sub>5sub>; GSK2894512-d<sub>5sub>

    		 Isotope-Labeled Compounds Aryl Hydrocarbon Receptor Inflammation/Immunology
    Tapinarof-d5 (WBI-1001-d5) is deuterium labeled Tapinarof. Tapinarof (WBI-1001) is a natural aryl hydrocarbon receptor (AhR) agonist with an EC50 of 13 nM. Tapinarof resolves skin inflammation in mice .
    Tapinarof-d5
  • HY-W022036S
    2-Ethoxyphenol-d5

    Guaethol-d<sub>5sub>; Guethol-d<sub>5sub>; NSC 180-d<sub>5sub>

    		 Isotope-Labeled Compounds Others
    2-Ethoxyphenol-d5 is the deuterium labeled 2-Ethoxyphenol .
    2-Ethoxyphenol-d5
  • HY-B0828S
    Triazophos-d5

    Hostathion 40EC-d<sub>5sub>; Hostathion-d<sub>5sub>; Hostation-d<sub>5sub>

    		 Isotope-Labeled Compounds Others
    Triazophos-d5 is the deuterium labeled Triazophos(HY-B0828) .
    Triazophos-d5
  • HY-16562AS
    Irinotecan-d5 hydrochloride

    (+)-Irinotecan-d<sub>5sub> hydrochloride; CPT-11-d<sub>5sub> hydrochloride; VAL-413-d<sub>5sub>

    		 Autophagy Topoisomerase Isotope-Labeled Compounds Cancer
    Irinotecan-d5 hydrochloride is deuterated labeled Irinotecan hydrochloride (HY-16562A). Irinotecan hydrochloride ((+)-Irinotecan hydrochloride) is a topoisomerase I inhibitor mainly used to treat colon cancer and rectal cancer .
    Irinotecan-d5 hydrochloride
  • HY-B1480S
    Ethoxzolamide-d5

    Redupresin-d<sub>5sub>; L-643786-d<sub>5sub>; PNU-4191-d<sub>5sub>

    		 Isotope-Labeled Compounds Carbonic Anhydrase Bacterial Infection Inflammation/Immunology
    Ethoxzolamide-d5 (Redupresin-d5) is deuterium labeled Ethoxzolamide. Ethoxzolamide is a carbonic anhydrase inhibitor with Ki of 1 nM.
    Ethoxzolamide-d5
  • HY-N0573S
    Umbelliferone-d5

    7-Hydroxycoumarin-d<sub>5sub>; Hydrangin-d<sub>5sub>; NSC 19790-d<sub>5sub>

    		 Isotope-Labeled Compounds Apoptosis Fluorescent Dye Neurological Disease Inflammation/Immunology Cancer
    Umbelliferone-d5 (7-Hydroxycoumarin-d5) is the deuterium labeled Umbelliferone (HY-N0573 ). Umbelliferone (7-Hydroxycoumarin), a natural orally active product of the coumarin family, is a fluorescing compound which can be used as a sunscreen agent. Umbelliferone induces cell cycle arrest, apoptosis and DNA fragmentation in HepG2 cells. Umbelliferone exhibits significant anticancer effects. Umbelliferone attenuates the alteration characteristics of allergic airway inflammation. Umbelliferone displays the neuroprotective effects and cross the blood-brain barrier. Umbelliferone exhibits anti-inflammatory and antioxidant effects in chronic alcohol-fed rats .
    Umbelliferone-d5
  • HY-13777S
    Zoledronic acid-d5

    Zoledronate-d<sub>5sub>; CGP 42446-d<sub>5sub>; CGP42446A-d<sub>5sub>; ZOL 446-d<sub>5sub>

    		 Bacterial Apoptosis Autophagy Isotope-Labeled Compounds Metabolic Disease Cancer
    Zoledronic acid-d5 is deuterated labeled Zoledronic Acid (HY-13777). Zoledronic Acid (Zoledronate) is a third-generation bisphosphonate (BP), with potent anti-resorptive activity. Zoledronic Acid inhibits the differentiation and apoptosis of osteoclasts. Zoledronic Acid also has anti-cancer effects .
    Zoledronic acid-d5
  • HY-125833
    Alpha-Naphthoflavone
    5+ Cited Publications

    		 Cytochrome P450 Aryl Hydrocarbon Receptor Apoptosis Cancer
    Alpha-Naphthoflavone is an orally active flavonoid that is a potent, competitive inhibitor of aromatase< b>aromatase. < b > IC < sub > 50 < / sub > < / b > and < b > K < sub > I < / sub > < / b > value were 0.5 and 0.2 microns. Alpha-Naphthoflavone can inhibit cell proliferation and induce apoptosis .
    Alpha-Naphthoflavone
  • HY-10570S3
    Nevirapine-d5

    BI-RG 587-d<sub>5sub>; NSC 641530-d<sub>5sub>; NVP-d<sub>5sub>

    		 Isotope-Labeled Compounds Infection Cancer
    Nevirapine-d5 (BI-RG 587-d5) is deuterium labeled Nevirapine. Nevirapine is a non-nucleoside inhibitor of HIV-1 reverse transcriptase used to treat and prevent HIV/AIDS; with a Ki of 270 μM .
    Nevirapine-d5
  • HY-B1207S
    Urethane-d5

    Ethyl carbamate-d<sub>5sub>; Carbamic acid ethyl ester-d<sub>5sub>; Ethylurethane-d<sub>5sub>

    		 Bacterial Parasite Infection Neurological Disease Cancer
    Urethane-d5 is the deuterium labeled Urethane. Urethane (Ethyl carbamate), the ethyl ester of carbamic acid, is a byproduct of fermentation found in various food products. Urethane has the ability to suppress bacterial, protozoal, sea urchin egg, and plant tissue growth in vitro .
    Urethane-d5
  • HY-77839S
    Cortodoxone-d5

    11-Deoxycortisol-d<sub>5sub>; cortexolone-d<sub>5sub>; Reichstein's substance S-d<sub>5sub>

    		 Isotope-Labeled Compounds Glucocorticoid Receptor Endogenous Metabolite Inflammation/Immunology Endocrinology
    Cortodoxone-d5 is the deuterium labeled Cortodoxone.
    Cortodoxone-d5
  • HY-14814S
    Delafloxacin-d5

    RX-3341-d<sub>5sub>; WQ-3034-d<sub>5sub>; ABT492-d<sub>5sub>

    		 Isotope-Labeled Compounds Bacterial Antibiotic Infection
    Delafloxacin-d5 is deuterium labeled Delafloxacin. Delafloxacin (RX-3341; WQ-3034; ABT492) is a broad-spectrum fluoroquinolone antibiotic. Delafloxacin has a broad spectrum of activity that includes drug-resistant Staphylococcus aureus, Streptococcus pneumoniae, and Klebsiella pneumonia .
    Delafloxacin-d5
  • HY-13636S1
    Fulvestrant-d5

    ICI 182780-d<sub>5sub>; ZD 9238-d<sub>5sub>; ZM 182780-d<sub>5sub>

    		 Isotope-Labeled Compounds Others
    Fulvestrant-d5 is a isotope of Fulvestrant .
    Fulvestrant-d5
  • HY-B1619S
    Cromolyn-d5

    Cromoglycate-d<sub>5sub>; Cromoglicic acid-d<sub>5sub>; FPL-670-d<sub>5sub> free acid

    		 Isotope-Labeled Compounds GSK-3 NF-κB Amyloid-β Neurological Disease Metabolic Disease Inflammation/Immunology Cancer
    Cromolyn-d5 (Cromoglycate-d5) is the deuterium labeled Cromolyn (HY-B1619). Cromolyn (Cromoglycate) is an orally active GSK-3β inhibitor with an IC50 of 2.0 μM. Cromolyn is also a mast cell stabilizer that can inhibit the release of mediators from mast cells, regulate reflex bronchoconstriction, and reduce non-specific bronchial hyperreactivity, and Cromolyn can be used in the research of bronchial asthma. In addition, Cromolyn has multiple activities such as anti-inflammatory, anti-allergic, anti-histamine, anti-cancer, and neuroprotective effects .
    Cromolyn-d5
  • HY-B0200D
    Cephalexin (lysine)

    Cefalexin (lysine); Cephacillin (lysine)

    		 Penicillin-binding protein (PBP) Bacterial Antibiotic Infection Cancer
    Cephalexin (Cefalexin) lysine is a potent, orally active new semisynthetic cephalosporin antibiotic with a broad antibacterial spectrum. Cephalexin lysine has antibacterial activity against a wide variety of gram-positive and gram-negative bacteria. Cephalexin lysine targets penicillin-binding proteins (PBPs) to inhibit bacterial cell wall assembly. Cephalexin lysine is used for the research of pneumonia, strep throat, and bacterial endocarditis, et al .
    Cephalexin (lysine)
  • HY-B0178AS1
    Guanidine-d5 hydrochloride

    Guanidinium-d<sub>5sub> chloride; Aminoformamidine-d<sub>5sub> hydrochloride

    		 Endogenous Metabolite Metabolic Disease
    Guanidine-d5 (hydrochloride) is the deuterium labeled Guanidine hydrochloride . Guanidine hydrochloride (Guanidinium chloride) a strong chaotrope, is also a strong denaturant of proteins .
    Guanidine-d5 hydrochloride
  • HY-B1487S1
    Procyclidine-d5

    Tricyclamol-d<sub>5sub>; (±)-Procyclidine-d<sub>5sub>

    		 Isotope-Labeled Compounds iGluR mAChR Neurological Disease
    Procyclidine-d5 (Tricyclamol-d5) is deuterium labeled Procyclidine (hydrochloride). Procyclidine (Tricyclamol, (±)-Procyclidine) hydrochloride , an anticholinergic agent, is a muscarinic receptor antagonist that also has the properties of an N-methyl-D-aspartate (NMDA) antagonist. Procyclidine hydrochloride can be used in studies of Parkinson's disease and related psychiatric disorders such as Soman-induced epilepsy .
    Procyclidine-d5
  • HY-W711852
    Benzamide-d5

    Benzenecarboxamide-d<sub>5sub>; Phenylamide-d<sub>5sub>

    		 Isotope-Labeled Compounds PARP Endogenous Metabolite Others
    Benzamide-d5 (Benzenecarboxamide-d5) is deuterium labeled Benzamide. Benzamide (Benzenecarboxamide) is a potent poly(ADP-ribose) polymerase (PARP) inhibitor. Benzamide has protective activity against both glutamate- and methamphetamine (METH)-induced neurotoxicity in vitro. Benzamide can attenuate the METH-induced dopamine depletions and exhibits neuroprotective activity in mice, also has no acute effect on striatal dopamine metabolism and does not reduce body temperature .
    Benzamide-d5
  • HY-B0878S
    Halobetasol propionate-d5

    BMY-30056-d<sub>5sub>; CGP-14458-d<sub>5sub>; Ulobetasol propionate-d<sub>5sub>

    		 Isotope-Labeled Compounds Glucocorticoid Receptor Inflammation/Immunology
    Halobetasol propionate-d5 (BMY-30056-d5) is deuterium labeled Halobetasol propionate (HY-B0878). Halobetasol propionate (BMY-30056) is a synthetic glucocorticoid corticosteroid. Halobetasol propionate exhibits anti-inflammatory, antipruritic, and vasoconstrictive properties. Halobetasol propionate can be used for the study of psoriasis .
    Halobetasol propionate-d5
  • HY-B1290S2
    2-Phenylethanol-d5

    Phenylethyl alcohol-d<sub>5sub>; Phenethyl alcohol-d<sub>5sub>; Benzyl carbinol-d<sub>5sub>

    		 Bacterial Virus Protease Antibiotic Infection
    2-Phenylethanol-d5 is the deuterium labeled 2-Phenylethanol . 2-Phenylethanol (Phenethyl alcohol), extracted from rose, carnation, hyacinth, Aleppo pine, orange blossom and other organisms, is a colourless liquid. It has a pleasant floral odor and also an autoantibiotic produced by the fungus Candida albicans . It is used as an additive in cigarettes and also used as a preservative in soaps due to its stability in basic conditions.
    2-Phenylethanol-d5
  • HY-N7745S1
    Glucosylsphingosine-d5

    Glucopsychosine-d<sub>5sub>; Lyso-Gb1-d<sub>5sub>; Lyso-GL1-d<sub>5sub>

    		 Isotope-Labeled Compounds Others
    Glucosylsphingosine-d5 is the deuterium labeled Glucosylsphingosine.
    Glucosylsphingosine-d5
  • HY-N0570S1
    Hydroxytyrosol-d5

    DOPET-d<sub>5sub>; 3,4-Dihydroxyphenethyl alcohol-d<sub>5sub>; 3-Hydroxytyrosol-d<sub>5sub>

    		 Endogenous Metabolite Bacterial Fungal Infection Inflammation/Immunology Cancer
    Hydroxytyrosol-d5 is the deuterium labeled Hydroxytyrosol. Hydroxytyrosol (DOPET) is a phenolic compound drawn from the olive tree and its leaves with anti-oxidant, anti-atherogenic, anti-thrombotic, antimicrobial, anti-inflammatory and anti-tumour effects .
    Hydroxytyrosol-d5
  • HY-B0941S
    6-Benzylaminopurine-d5

    Benzyladenine-d<sub>5sub>; 6-BAP-d<sub>5sub>; N6-Benzyladenine-d<sub>5sub>

    		 Endogenous Metabolite Isotope-Labeled Compounds Others
    6-Benzylaminopurine-d5 is the deuterium labeled 6-Benzylaminopurine. 6-Benzylaminopurine is a cytokinin .
    6-Benzylaminopurine-d5
  • HY-B0521S
    Altrenogest-d5

    Allyltrenbolone-d<sub>5sub>; RU2267-d<sub>5sub>

    		 Progesterone Receptor Endocrinology
    Altrenogest-d5 is the deuterium labeled Altrenogest. Altrenogest (Allyltrenbolone) is a progestogen structurally related to veterinary steroid trenbolone.
    Altrenogest-d5
  • HY-12199BS
    Pitolisant-d5 hydrochloride

    Ciproxidine-d<sub>5sub> hydrochloride; BF 2649-d<sub>5sub> hydrochloride

    		 Histamine Receptor Isotope-Labeled Compounds Neurological Disease Endocrinology
    Pitolisant-d5 hydrochloride (Ciproxidine-d5 hydrochloride) is the deuterium labeled Pitolisant hydrochloride (HY-12199B). Pitolisant hydrochloride is a potent and selective nonimidazole inverse agonist at the recombinant human histamine H3 receptor (Ki=0.16 nM) .
    Pitolisant-d5 hydrochloride

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