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27-Hydroxy cholesterol-d<sub>6</sub>

" in MedChemExpress (MCE) Product Catalog:

2815

Inhibitors & Agonists

9

Biochemical Assay Reagents

11

Peptides

1

Inhibitory Antibodies

8

Natural
Products

7

Recombinant Proteins

2746

Isotope-Labeled Compounds

3

Antibodies

14

Click Chemistry

Targets Recommended:
Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-113342S
    7-Keto Cholesterol-d7

    		Endogenous Metabolite Isotope-Labeled Compounds Others
    7-Keto Cholesterol-d7 is the deuterium labeled 7-Keto Cholesterol[1].
    7-Keto <em>Cholesterol-d</em>7
  • HY-143367S
    27-Hydroxy cholesterol-d6

    		Isotope-Labeled Compounds Others
    27-Hydroxy cholesterol-d6 is deuterium labeled 27-Hydroxy cholesterol.
    <em>27-Hydroxy</em> <em>cholesterol-d</em><em>6</em>
  • 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-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-N10888
    (22R)-27-Hydroxy-1-oxowitha-2,5,24-trienolide

    		Others Others
    (22R)-27-Hydroxy-1-oxowitha-2,5,24-trienolide, withanolide, is a natural product. (22R)-27-Hydroxy-1-oxowitha-2,5,24-trienolide can be isolated from the aerial parts of the halophyte Datura stramonium .
    (22R)-<em>27-Hydroxy</em>-1-oxowitha-2,5,24-trienolide
  • HY-N0322S7
    Cholesterol-d1

    		Isotope-Labeled Compounds Estrogen Receptor/ERR Endogenous Metabolite Endocrinology
    Cholesterol-d is the deuterium labeled Cholesterol. Cholesterol is the major sterol in mammals. It is making up 20-25% of structural component of the plasma membrane. Plasma membranes are highly permeable to water but relatively impermeable to ions and protons. Cholesterol plays an important role in determining the fluidity and permeability characteristics of the membrane as well as the function of both the transporters and signaling proteins . Cholesterol is also an endogenous estrogen-related receptor α (ERRα) agonist .
    <em>Cholesterol-d</em>1
  • HY-N0322S
    Cholesterol-d7

    		Estrogen Receptor/ERR Endogenous Metabolite Metabolic Disease
    Cholesterol-d7 is the deuterium labeled Cholesterol. Cholesterol is the major sterol in mammals. It is making up 20-25% of structural component of the plasma membrane. Plasma membranes are highly permeable to water but relatively impermeable to ions and protons. Cholesterol plays an important role in determining the fluidity and permeability characteristics of the membrane as well as the function of both the transporters and signaling proteins . Cholesterol is also an endogenous estrogen-related receptor α (ERRα) agonist .
    <em>Cholesterol-d</em>7
  • HY-N0322S1
    Cholesterol-d6

    		Estrogen Receptor/ERR Endogenous Metabolite Metabolic Disease
    Cholesterol-d6 is the deuterium labeled Cholesterol. Cholesterol is the major sterol in mammals. It is making up 20-25% of structural component of the plasma membrane. Plasma membranes are highly permeable to water but relatively impermeable to ions and protons. Cholesterol plays an important role in determining the fluidity and permeability characteristics of the membrane as well as the function of both the transporters and signaling proteins . Cholesterol is also an endogenous estrogen-related receptor α (ERRα) agonist .
    <em>Cholesterol-d</em><em>6</em>
  • HY-N0322S6
    Cholesterol-d4

    		Estrogen Receptor/ERR Endogenous Metabolite Metabolic Disease
    Cholesterol-d4 is deuterium labeled Cholesterol. Cholesterol is the major sterol in mammals. It is making up 20-25% of structural component of the plasma membrane. Plasma membranes are highly permeable to water but relatively impermeable to ions and protons. Cholesterol plays an important role in determining the fluidity and permeability characteristics of the membrane as well as the function of both the transporters and signaling proteins . Cholesterol is also an endogenous estrogen-related receptor α (ERRα) agonist .
    <em>Cholesterol-d</em>4
  • HY-N0322S2
    Cholesterol-d6-1

    		Isotope-Labeled Compounds Estrogen Receptor/ERR Endogenous Metabolite Metabolic Disease
    Cholesterol-d6-1 is the deuterium labeled Cholesterol. Cholesterol is the major sterol in mammals. It is making up 20-25% of structural component of the plasma membrane. Plasma membranes are highly permeable to water but relatively impermeable to ions and protons. Cholesterol plays an important role in determining the fluidity and permeability characteristics of the membrane as well as the function of both the transporters and signaling proteins . Cholesterol is also an endogenous estrogen-related receptor α (ERRα) agonist .
    <em>Cholesterol-d</em><em>6</em>-1
  • 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-B0715S
    Pentoxifylline-d6

    BL-191-d<sub>6sub>; PTX-d<sub>6sub>; Oxpentifylline-d<sub>6sub>

    		 Phosphodiesterase (PDE) Autophagy HIV Cardiovascular Disease Cancer
    Pentoxifylline-d6 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[1][2][3].
    Pentoxifylline-d<em>6</em>
  • HY-15494S1
    Picropodophyllin-d6

    AXL1717-d<sub>6sub>; Picropodophyllotoxin-d<sub>6sub>; PPP-d<sub>6sub>

    		 Isotope-Labeled Compounds IGF-1R Apoptosis Endocrinology Cancer
    Picropodophyllin-d6 (AXL1717-d6) is deuterium labeled Picropodophyllin. Picropodophyllin (AXL1717) is a selective insulin-like growth factor-1 receptor (IGF-1R) inhibitor with an IC50 of 1 nM.
    Picropodophyllin-d<em>6</em>
  • HY-B1873S
    Methoxychlor-d6

    DMDT-d<sub>6sub>; Methoxcide-d<sub>6sub>; Methoxy-DDT-d<sub>6sub>

    		 Isotope-Labeled Compounds Others
    Methoxychlor-d6 is the deuterium labeled Methoxychlor[1].
    Methoxychlor-d<em>6</em>
  • HY-B0236S
    6-Aminocaproic acid-d6

    EACA-d<sub>6sub>; Epsilon-Amino-n-caproic acid-d<sub>6sub>; 6-Aminohexanoic acid-d<sub>6sub>

    		 Isotope-Labeled Compounds Metabolic Disease
    6-Aminocaproic acid-d6 is deuterium labeled 6-Aminocaproic acid. 6-Aminocaproic acid (EACA), a monoamino carboxylic acid, is a potent and orally active inhibitor of plasmin and plasminogen. 6-Aminocaproic acid is a potent antifibrinolytic agent. 6-Aminocaproic acid prevents clot lysis through the competitive binding of lysine residues on plasminogen, inhibiting plasmin formation and reducing fibrinolysis. 6-Aminocaproic acid can be used for the research of bleeding disorders[1][2].
    <em>6</em>-Aminocaproic acid-d<em>6</em>
  • HY-76542S
    Vitamin D2-d6

    Ergocalciferol-d<sub>6sub>; Calciferol-d<sub>6sub>; Ercalciol-d<sub>6sub>

    		 VD/VDR Endogenous Metabolite Metabolic Disease
    Vitamin D2-d6 is the deuterium labeled Vitamin D2. Vitamin D2 (Ergocalciferol), drived from plant sources or dietary supplements, could be used as supplement of Vitamin D[1][2].
    Vitamin D2-d<em>6</em>
  • HY-N0537S9
    Xylose-d6

    D-(+)-Xylose-d<sub>6sub>; (+)-Xylose-d<sub>6sub>; Wood sugar-d<sub>6sub>

    		 Isotope-Labeled Compounds Endogenous Metabolite Others
    Xylose-d6 is the deuterium labeled Xylose.
    Xylose-d<em>6</em>
  • HY-N1214S
    Squalene-d6

    Super Squalene-d<sub>6sub>; trans-Squalene-d<sub>6sub>; AddaVax-d<sub>6sub>

    		 Isotope-Labeled Compounds Others
    Squalene-d6 is a deuterium labeled Squalene. Squalene (Super Squalene) is an intermediate product in the synthesis of cholesterol, and shows several pharmacological properties such as hypolipidemic, hepatoprotective, antiatherosclerotic, cardioprotective, antioxidant, and antitumour activity .
    Squalene-d<em>6</em>
  • HY-41681S
    6-Chloro-1-hexanol-d6

    1-Chloro-6-hexanol-d<sub>6sub>; 1-Chloro-6-Hydroxyhexane-d<sub>6sub>; 6-Chlorohexanol-d<sub>6sub>

    		 Isotope-Labeled Compounds Others
    6-Chloro-1-hexanol-d6 is the deuterium labeled 6-Chloro-1-hexanol[1].
    <em>6</em>-Chloro-1-hexanol-d<em>6</em>
  • HY-12008S
    Erlotinib-d6 hydrochloride

    CP-358774-d<sub>6sub> hydrochloride; NSC 718781-d<sub>6sub> hydrochloride; OSI-774-d<sub>6sub> hydrochloride

    		 EGFR Autophagy Cancer
    Erlotinib-d6 (hydrochloride) a deuterium labeled Erlotinib Hydrochloride. Erlotinib Hydrochloride inhibits purified EGFR kinase with an IC50 of 2 nM[1]. Erlotinib-d6 (hydrochloride) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    Erlotinib-d<em>6</em> hydrochloride
  • HY-50896S
    Erlotinib-d6

    CP-358774-d<sub>6sub>; NSC 718781-d<sub>6sub>; OSI-774-d<sub>6sub>

    		 EGFR Cancer
    Erlotinib-d6 (CP-358774 D6) is a deuterium labeled Erlotinib (CP-358774). Erlotinib is a directly acting inhibitor EGFR tyrosine kinase inhibitor with an IC50 of 2 nM for human EGFR[1]. Erlotinib-d6 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    Erlotinib-d<em>6</em>
  • HY-N0005S
    Curcumin-d6

    Diferuloylmethane-d<sub>6sub>; Natural Yellow 3-d<sub>6sub>; Turmeric yellow-d<sub>6sub>

    		 Keap1-Nrf2 Ferroptosis Autophagy Histone Acetyltransferase Epigenetic Reader Domain Mitophagy Influenza Virus Infection Metabolic Disease Inflammation/Immunology
    Curcumin-d6is a deuterium labeled Curcumin (Turmeric yellow). Curcumin (Turmeric yellow) is a natural phenolic compound with diverse pharmacologic effects including anti-inflammatory, antioxidant, antiproliferative and antiangiogenic activities. Curcumin is an inhibitor of p300 histone acetylatransferase (HATs) and also shows inhibitory effects on NF-κB and MAPKs.
    Curcumin-d<em>6</em>
  • HY-12176AS
    Aliskiren-d6 hydrochloride

    CGP 60536-d<sub>6sub> Hydrochloride; CGP60536Bd<sub>6sub> Hydrochloride; SPP 100d<sub>6sub>(Hydrochloride)

    		 Isotope-Labeled Compounds Renin Cardiovascular Disease Cancer
    Aliskiren-d6 (hydrochloride) is is deuterium labeled Aliskiren, which is a direct renin inhibitor.
    Aliskiren-d<em>6</em> hydrochloride
  • HY-13011S1
    Alectinib-d6

    CH5424802-d<sub>6sub>; RO5424802-d<sub>6sub>; AF802-d<sub>6sub>

    		 Isotope-Labeled Compounds Anaplastic lymphoma kinase (ALK) Cancer
    Alectinib-d6 is deuterium labeled Alectinib. Alectinib (CH5424802) is a potent, selective, and orally available ALK inhibitor with an IC50 of 1.9 nM and a Kd value of 2.4 nM (in an ATP-competitive manner), and also inhibits ALK F1174L and ALK R1275Q with IC50s of 1 nM and 3.5 nM, respectively[1]. Alectinib demonstrates effective central nervous system (CNS) penetration[2].
    Alectinib-d<em>6</em>
  • HY-100977S
    Dimethoxycurcumin-d6

    DiMC-d<sub>6sub>; CHC 004-d<sub>6sub>; Di-O-methylcurcumin-d<sub>6sub>

    		 Isotope-Labeled Compounds Inflammation/Immunology
    Dimethoxycurcumin-d6 is the deuterium labeled Dimethoxycurcumin (HY-100977). Dimethoxycurcumin is a derivative of Curcumin that has anti-inflammatory and antioxidant activities .
    Dimethoxycurcumin-d<em>6</em>
  • HY-19655S
    Cethromycin-d6

    ABT-773-d<sub>6sub>; Abbott-195773-d<sub>6sub>; A-195773-d<sub>6sub>

    		 Bacterial Isotope-Labeled Compounds Inflammation/Immunology
    Cethromycin-d6 (ABT-773-d6; Abbott-195773-d6; A-195773-d6) is deuterium-labeled Cethromycin (HY-19655) .
    Cethromycin-d<em>6</em>
  • HY-N0113S
    Hordenine-d6

    Ordenina-d<sub>6sub>; Peyocactine-d<sub>6sub>

    		 Isotope-Labeled Compounds Bacterial Antibiotic Infection Cardiovascular Disease
    Hordenine-d6 (Ordenina-d6) is the deuterium labeled Hordenine. Hordenine, an alkaloid found in plants, inhibits melanogenesis by suppression of cyclic adenosine monophosphate (cAMP) production .
    Hordenine-d<em>6</em>
  • HY-N0283S
    Diacerein-d6

    Diacerhein-d<sub>6sub>; Diacetylrhein-d<sub>6sub>

    		 Interleukin Related Inflammation/Immunology
    Diacerein-d6 is the deuterium labeled Diacerein[1]. Diacerein (Diacerhein), a interleukin-1 beta inhibitor, is a slow-acting medicine of the class anthraquinone used to treat joint diseases[2].
    Diacerein-d<em>6</em>
  • HY-N0113BS
    Hordenine-d6 hydrochloride

    Ordenina-d<sub>6sub> hydrochloride; Peyocactine-d<sub>6sub> hydrochloride

    		 Antibiotic Isotope-Labeled Compounds Infection
    Hordenine-d6 (Ordenina-d6; Peyocactine-d6) hydrochloride is deuterium-labeled Hordenine (hydrochloride) (HY-N0113B) .
    Hordenine-d<em>6</em> hydrochloride
  • HY-Y0504S4
    Trimethylammonium chloride-d6

    Hegzadesil-d<sub>6sub>; Trimethylamine hydrochloric acid-d<sub>6sub>; Trimethylamine monohydrochloride-d<sub>6sub>

    		 Endogenous Metabolite Metabolic Disease
    Trimethylammonium chloride-d6 is the deuterium labeled Trimethylammonium chloride[1]. Trimethylammonium chloride is an endogenous metabolite.
    Trimethylammonium chloride-d<em>6</em>
  • HY-B0005S1
    Toremifene-d6 hydrochloride

    Z-Toremifene-d<sub>6sub> hydrochloride; NK 622-d<sub>6sub> hydrochloride; FC-1157a-d<sub>6sub> hydrochloride

    		 Isotope-Labeled Compounds Estrogen Receptor/ERR Infection
    Toremifene-d6 (Z-Toremifene-d6) hydrochloride is deuterium labeled Toremifene. Toremifene is a second-generation selective estrogen-receptor modulator (SERM) in development for the prevention of osteoporosis. Toremifene also potent inhibits infectious EBOV Zaire and Marburg (MARV) with IC50 of 0.07 µM and 2.6 µM, respectively .
    Toremifene-d<em>6</em> hydrochloride
  • HY-19489S
    (±)-Levomepromazine-d6

    (±)-Methotrimeprazine-d<sub>6sub>; dl-Methotrimeprazine-d<sub>6sub>

    		 Dopamine Receptor Histamine Receptor Neurological Disease
    (±)-Levomepromazine-d6 is the deuterium labeled Methotrimeprazine, which is a D3 dopamine and Histamine H1 receptor antagonist.
    (±)-Levomepromazine-d<em>6</em>
  • HY-90001S
    Ritonavir-d6

    ABT 538-d<sub>6sub>; RTV-d<sub>6sub>

    		 HIV Protease HIV SARS-CoV Apoptosis Infection
    Ritonavir-d6 is the deuterium labeled Ritonavir. Ritonavir (ABT 538) is an inhibitor of HIV protease used to treat HIV infection and AIDS. Ritonavir is also a SARS-CoV 3CLpro inhibitor with an IC50 of 1.61 μM[1][2].
    Ritonavir-d<em>6</em>
  • HY-15772S
    Osimertinib-d6

    AZD-9291-d<sub>6sub>; Mereletinib-d<sub>6sub>

    		 EGFR Cancer
    Osimertinib-d6 is a deuterium labeled osimertinib. Osimertinib is a covalent, orally active, irreversible, and mutant-selective EGFR inhibitor with an apparent IC50 of 12 nM against L858R and 1 nM against L858R/T790M. Osimertinib overcomes T790M-mediated resistance to EGFR inhibitors in lung cancer[1].
    Osimertinib-d<em>6</em>
  • HY-B1438S
    Canrenone-d6

    Aldadiene-d<sub>6sub>; SC9376-d<sub>6sub>

    		 Isotope-Labeled Compounds Mineralocorticoid Receptor Endogenous Metabolite Cardiovascular Disease
    Canrenone-d6 is the deuterium labeled Canrenone. Canrenone (Aldadiene) is an aldosterone antagonist extensively used as a diuretic agent.
    Canrenone-d<em>6</em>
  • HY-N0614S
    Sucralose-d6

    E955-d<sub>6sub>; Trichlorosucrose-d<sub>6sub>

    		 Endogenous Metabolite Cancer
    Sucralose-d6 is deuterium labeled Sucralose. Sucralose (E955; Trichlorosucrose) is a non-nutritive artificial sweetener and sugar substitute. Sucralose can activate a conserved neural fasting response and thereby exerts an appetite-stimulating effect in rodents[1][2].
    Sucralose-d<em>6</em>
  • HY-116152S
    Cipepofol-d6

    Ciprofol-d<sub>6sub>; HSK3486-d<sub>6sub>

    		 Isotope-Labeled Compounds GABA Receptor Neurological Disease
    Cipepofol-d6 (Ciprofol-d6; HSK3486-d6) is deuterium labeled Cipepofol (HY-116152). Cipepofol (HSK3486), a psychomotor stabilizing agent, is a gamma-aminobutyric acid (GABA) receptor potentiator.
    Cipepofol-d<em>6</em>
  • HY-15459S
    Cabazitaxel-d6

    XRP6258-d<sub>6sub>; RPR-116258A-d<sub>6sub>; taxoid XRP6258-d<sub>6sub>

    		 Microtubule/Tubulin Autophagy Cancer
    Cabazitaxel-d6 is the deuterium labeled Cabazitaxel. Cabazitaxel is a semi-synthetic derivative of the natural taxoid 10-deacetylbaccatin III with potential antineoplastic activity[1][2].
    Cabazitaxel-d<em>6</em>
  • HY-B0457S1
    Clomipramine-d6 hydrochloride

    Chlorimipramine-d<sub>6sub> (hydrochloride); G-34586-d<sub>6sub> (hydrochloride); NSC-169865-d<sub>6sub> (hydrochloride)

    		 Serotonin Transporter Neurological Disease
    Clomipramine-d6 (hydrochloride) is the deuterium labeled Clomipramine hydrochloride. Clomipramine (Chlorimipramine) hydrochloride is a potent 5-HT reuptake blocker with the IC50 value of 1.5 nM. Clomipramine hydrochloride is a tricyclic antidepressant that can be used for the research of depression and obsessive compulsive disorder (OCD)[1].
    Clomipramine-d<em>6</em> hydrochloride
  • HY-N0488S2
    Vincristine-d6 sulfate

    Leurocristine-d<sub>6sub> sulfate; NSC-67574-d<sub>6sub> sulfate; 22-Oxovincaleukoblastine-d<sub>6sub> sulfate

    		 Isotope-Labeled Compounds Microtubule/Tubulin Apoptosis Cancer
    Vincristine-d6 (sulfate) is the deuterium labeled Vincristine sulfate. Vincristine sulfate is an antitumor vinca alkaloid which inhibits microtubule formation in mitotic spindle, resulting in an arrest of dividing cells at the metaphase stage. It binds to microtubule with a Ki of 85 nM.
    Vincristine-d<em>6</em> sulfate
  • HY-14649S3
    Retinoic acid-d6

    Vitamin A acid-d<sub>6sub>; all-trans-Retinoic acid-d<sub>6sub>; ATRA-d<sub>6sub>

    		 RAR/RXR PPAR Autophagy Endogenous Metabolite Cancer
    Retinoic acid-d6 is the deuterium labeled Retinoic acid[1]. Retinoic acid is a metabolite of vitamin A that plays important roles in cell growth, differentiation, and organogenesis. Retinoic acid is a natural agonist of RAR nuclear receptors, with IC50s of 14 nM for RARα/β/γ. Retinoic acid bind to PPARβ/δ with Kd of 17 nM. Retinoic acid acts as an inhibitor of transcription factor Nrf2 through activation of retinoic acid receptor alpha[2][3][4][5][6][7].
    Retinoic acid-d<em>6</em>
  • HY-D0931S
    Sudan III-d6

    Sudan Red III-d<sub>6sub>; Tetrazobenzene-β-naphthol-d<sub>6sub>; 111440 Red-d<sub>6sub>

    		 Isotope-Labeled Compounds Others
    Sudan III-d6 (Sudan Red III-d6; Tetrazobenzene-β-naphthol-d6) is a deuterium labeled Sudan III (HY-D0931). Sudan III is a hydrophobic bisazo dye .
    Sudan III-d<em>6</em>
  • HY-B0801S
    Fexofenadine-d6
    2 Publications Verification

    MDL-16455-d<sub>6sub>; Terfenadine carboxylate-d<sub>6sub>

    		 Histamine Receptor Inflammation/Immunology Endocrinology
    Fexofenadine-d6 is deuterium labeled Fexofenadine, which is an antihistamine pharmaceutical agent.
    Fexofenadine-d<em>6</em>
  • HY-116578S
    Metopimazine-d6

    EXP999-d<sub>6sub>; RP9965-d<sub>6sub>

    		 Isotope-Labeled Compounds Others
    Metopimazine-d6 is the deuterium labeled Metopimazine[1].
    Metopimazine-d<em>6</em>
  • HY-B1118S
    Secnidazole-d6

    RP-14539-d<sub>6sub>; PM-185184-d<sub>6sub>

    		 Parasite Antibiotic Infection
    Secnidazole-d6 is the deuterium labeled Secnidazole. Secnidazole (RP-14539;PM-185184) is an orally active azole antibiotic with a longer half-life than metronidazole (HY-B0318). Secnidazole is against the vaginosis-associated bacteria and has the potential for bacterial vaginosis research[1].
    Secnidazole-d<em>6</em>
  • HY-13016S
    Cabozantinib-d6

    XL184-d<sub>6sub>; BMS-907351-d<sub>6sub>

    		 VEGFR c-Met/HGFR c-Kit TAM Receptor FLT3 Apoptosis Cancer
    Cabozantinib-d6 is the deuterium labeled Cabozantinib. Cabozantinib is a potent multiple receptor tyrosine kinases (RTKs) inhibitor that inhibits VEGFR2, c-Met, Kit, Axl and Flt3 with IC50s of 0.035, 1.3, 4.6, 7 and 11.3 nM, respectively[1][2][3].
    Cabozantinib-d<em>6</em>
  • HY-13677S
    6-Mercaptopurine-d2

    Mercaptopurine-d<sub>2sub>; 6-MP-d<sub>2sub>

    		 Isotope-Labeled Compounds Nucleoside Antimetabolite/Analog Autophagy Endogenous Metabolite Cancer
    6-Mercaptopurine-d2 is the deuterium labeled 6-Mercaptopurine. 6-Mercaptopurine is a purine analogue which acts as an antagonist of the endogenous purines and has been widely used as antileukemic agent and immunosuppressive agent[1][2].
    <em>6</em>-Mercaptopurine-d2
  • HY-B0110S
    Gestodene-d6

    SHB 331-d<sub>6sub>; WL 70-d<sub>6sub>

    		 Isotope-Labeled Compounds Progesterone Receptor Endocrinology
    Gestodene-d6is the deuterium labeled Gestodene. Gestodene(SHB 331) is a progestogen hormonal contraceptive[1][2]. Gestodene-d6 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    Gestodene-d<em>6</em>
  • HY-76511S
    Verlukast-d6

    MK-679-d<sub>6sub>; L 668019-d<sub>6sub>

    		 Leukotriene Receptor Inflammation/Immunology
    Verlukast-d6 is a deuterium labeled Verlukast. Verlukast is a potent, selective, and orally active antagonist of leukotriene receptor. Verlukast has the potential for the research of asthma[1].
    Verlukast-d<em>6</em>
  • HY-B1350S
    Fusidic acid-d6

    Fusidate-d<sub>6sub>; SQ-16603-d<sub>6sub>

    		 Bacterial Antibiotic Infection
    Fusidic acid-d6 is the deuterium labeled Fusidic acid. Fusidic acid (Fusidate) a bacteriostatic antibiotic produced from the Fusidium coccineum fungus, belongs to the class of steroids. Fusidic acid has no corticosteroid effects. Fusidic acid inhibits the growth of bacteria by preventing the release of translation elongation factor G (EF-G) from the ribosome[1][2].
    Fusidic acid-d<em>6</em>

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