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Bisphenol A-d<sub>14</sub>

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3019

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Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-18260S1

    Endogenous Metabolite Endocrinology
    Bisphenol A-d6 is the deuterium labeled Bisphenol A. Bisphenol A is a phenolic, organic synthetic compound widely used in the production of polycarbonate plastics and epoxy resins. Bisphenol A is a reproductive, developmental, and systemic toxicant, often classified as an endocrine-disrupting compound (EDC). Bisphenol A is associated with many diseases, including cardiovascular diseases, respiratory diseases, diabetes, kidney diseases, obesity, and reproductivedisorders[1][2][3].
    <em>Bisphenol</em> <em>A-d</em>6
  • HY-18260S

    Endogenous Metabolite Endocrinology
    Bisphenol A-d16 is the deuterium labeled Bisphenol A[1]. Bisphenol A is a phenolic, organic synthetic compound widely used in the production of polycarbonate plastics and epoxy resins. Bisphenol A is a reproductive, developmental, and systemic toxicant, often classified as an endocrine-disrupting compound (EDC). Bisphenol A is associated with many diseases, including cardiovascular diseases, respiratory diseases, diabetes, kidney diseases, obesity, and reproductivedisorders[2][3].
    <em>Bisphenol</em> <em>A-d</em>16
  • HY-18260S4

    Endogenous Metabolite Endocrinology
    Bisphenol A-d4 is the deuterium labeled Bisphenol A[1]. Bisphenol A is a phenolic, organic synthetic compound widely used in the production of polycarbonate plastics and epoxy resins. Bisphenol A is a reproductive, developmental, and systemic toxicant, often classified as an endocrine-disrupting compound (EDC). Bisphenol A is associated with many diseases, including cardiovascular diseases, respiratory diseases, diabetes, kidney diseases, obesity, and reproductivedisorders[2][3].
    <em>Bisphenol</em> <em>A-d</em>4
  • HY-W654078

    BPAF-13C<sub>12sub>; 4,4'-(Perfluoropropane-2,2-diyl)diphenol-13C<sub>12sub>

    Isotope-Labeled Compounds Others
    Bisphenol AF- 13C12 is an isotopic label of Bisphenol AF. Bisphenol AF is used in polycarbonate plastic and epoxy resin manufacturing. Bisphenol AF can significantly increase intracellular ROS levels .
    <em>Bisphenol</em> AF-13C12
  • HY-18260S6

    Isotope-Labeled Compounds Endocrinology
    Bisphenol A-d14 is a deuterium labeled Bisphenol A (HY-18260). Bisphenol A is a phenolic, organic synthetic compound widely used in the production of polycarbonate plastics and epoxy resins. Bisphenol A is a reproductive, developmental, and systemic toxicant, often classified as an endocrine-disrupting compound (EDC). Bisphenol A is associated with many diseases, including cardiovascular diseases, respiratory diseases, diabetes, kidney diseases, obesity, and reproductivedisorders .
    <em>Bisphenol</em> <em>A-d</em><em>14</em>
  • HY-18260S3

    Endogenous Metabolite Endocrinology
    Bisphenol A-d8 is the deuterium labeled Bisphenol A[1]. Bisphenol A is a phenolic, organic synthetic compound widely used in the production of polycarbonate plastics and epoxy resins. Bisphenol A is a reproductive, developmental, and systemic toxicant, often classified as an endocrine-disrupting compound (EDC). Bisphenol A is associated with many diseases, including cardiovascular diseases, respiratory diseases, diabetes, kidney diseases, obesity, and reproductivedisorders[2][3][4].
    <em>Bisphenol</em> <em>A-d</em>8
  • HY-150988S

    Isotope-Labeled Compounds Others
    2,2'-Dichloro bisphenol A-d12 is the deuterium labeled 2,2'-Dichloro bisphenol A[1].
    2,2'-Dichloro <em>bisphenol</em> <em>A-d</em>12
  • HY-150992S

    Isotope-Labeled Compounds Others
    2,6-Dichloro bisphenol A-d12 is the deuterium labeled 2,6-Dichloro bisphenol A[1].
    2,6-Dichloro <em>bisphenol</em> <em>A-d</em>12
  • HY-18260S5

    Endogenous Metabolite Endocrinology
    Bisphenol A-d4-1 is the deuterium labeled Bisphenol A[1]. Bisphenol A is a phenolic, organic synthetic compound widely used in the production of polycarbonate plastics and epoxy resins. Bisphenol A is a reproductive, developmental, and systemic toxicant, often classified as an endocrine-disrupting compound (EDC). Bisphenol A is associated with many diseases, including cardiovascular diseases, respiratory diseases, diabetes, kidney diseases, obesity, and reproductivedisorders[2][3].
    <em>Bisphenol</em> <em>A-d</em>4-1
  • HY-150987S

    Isotope-Labeled Compounds Others
    2,2',6-Trichloro bisphenol A-d11 is the deuterium labeled 2,2',6-Trichloro bisphenol A[1].
    2,2',6-Trichloro <em>bisphenol</em> <em>A-d</em>11
  • HY-N12840

    Others Metabolic Disease
    Logmalicid B is an iridoid glycoside compound that can be isolated from Cornus officinalis and can be used in diabetes research .
    Logmalicid B
  • HY-W654077

    BPAF-d<sub>4sub>; 4,4'-(Perfluoropropane-2,2-diyl)diphenol-d<sub>4sub>

    Estrogen Receptor/ERR Endocrinology
    Bisphenol AF-d4 is the isotope labelled analog of Bisphenol AF (HY-W013782). Bisphenol AF is a full agonist for the estrogen receptor. Bisphenol AF acts as an endocrine-disrupting chemical (EDC), activating estrogen through the estrogen receptor Era. Bisphenol AF-d4 can be used for the research of endocrinology and cancer .
    <em>Bisphenol</em> AF-d4
  • HY-18260R

    Endogenous Metabolite Endocrinology
    Bisphenol A (Standard) is the analytical standard of Bisphenol A. This product is intended for research and analytical applications. Bisphenol A is a phenolic, organic synthetic compound widely used in the production of polycarbonate plastics and epoxy resins. Bisphenol A is a reproductive, developmental, and systemic toxicant, often classified as an endocrine-disrupting compound (EDC). Bisphenol A is associated with many diseases, including cardiovascular diseases, respiratory diseases, diabetes, kidney diseases, obesity, and reproductivedisorders .
    <em>Bisphenol</em> A (Standard)
  • HY-W013935

    Endogenous Metabolite Endocrinology
    Bisphenol B is a very close structural analog of Bisphenol A (HY-18260), an endocrine disrupting chemical (EDC) and a substance of very high concern (SVHC) in the European Union (EU) for both human health. Bisphenol B shows endocrine disruptive properties or other adverse effects on animal models .
    <em>Bisphenol</em> B
  • HY-W008628S

    Isotope-Labeled Compounds Others
    Bisphenol AP-d5 is the deuterium labeled Bisphenol AP[1].
    <em>Bisphenol</em> AP-d5
  • HY-18260
    Bisphenol A
    5+ Cited Publications

    Endogenous Metabolite Endocrinology
    Bisphenol A is a phenolic, organic synthetic compound widely used in the production of polycarbonate plastics and epoxy resins. Bisphenol A is a reproductive, developmental, and systemic toxicant, often classified as an endocrine-disrupting compound (EDC). Bisphenol A is associated with many diseases, including cardiovascular diseases, respiratory diseases, diabetes, kidney diseases, obesity, and reproductivedisorders .
    <em>Bisphenol</em> A
  • HY-142555S

    Isotope-Labeled Compounds Others
    Bisphenol A monosulfate-d6 (sodium) is the deuterium labeled Bisphenol A monosulfate sodium[1].
    <em>Bisphenol</em> A monosulfate-d6 sodium
  • HY-115746

    DMBPA

    HIF/HIF Prolyl-Hydroxylase Cancer
    Dimethyl-bisphenol A (DMBPA) is a potent HIF-1α inhibitor. Dimethyl-bisphenol A can decrease Vegfa mRNA expression .
    Dimethyl-<em>bisphenol</em> A
  • HY-161116

    Others Cancer
    AD-5584 is an ACSS2 inhibitor with blood-brain permeability. AD-5584 can significantly reduce lipid storage, reduce colony formation, and increase cell death. AD-5584 has antitumor activity .
    <em>AD</em>-5584
  • HY-161117

    Others Cancer
    AD-8007 is an acetyl CoA synthase 2 (ACSS2) inhibitor that can cross the blood-brain barrier. AD-8007 can significantly reduce lipid storage and cell colony formation in vitro models, and increase tumor cell death. AD-8007 has anti-cancer activity and can be used in the research of breast cancer .
    <em>AD</em>-8007
  • HY-150985S

    Isotope-Labeled Compounds Others
    2,2'-Dichloro bisphenol a mono-D-glucuronide-d12 is the deuterium labeled 2,2'-Dichloro bisphenol a mono-D-glucuronide[1].
    2,2'-Dichloro <em>bisphenol</em> a mono-D-glucuronide-d12
  • HY-W013326S

    Isotope-Labeled Compounds Others
    Bisphenol Z-d6is the deuterium labeled4,4'-(Cyclohexane-1,1-diyl)diphenol(HY-W013326) .
    <em>Bisphenol</em> Z-d6
  • HY-143886

    Angiotensin-converting Enzyme (ACE) Cardiovascular Disease
    AD011 is a dual inhibitor of cACE/NEP. AD011 is synthesized based on the previously reported C-domain selective ACE inhibitor lisinopril-tryptophan. AD011 has the potential for providing the potent antihypertensive and cardioprotective benefits .
    <em>AD</em>011
  • HY-143887

    Angiotensin-converting Enzyme (ACE) Cardiovascular Disease
    AD012 is a dual inhibitor of cACE/NEP. AD012 is synthesized based on the previously reported C-domain selective ACE inhibitor lisinopril-tryptophan. AD012 has the potential for providing the potent antihypertensive and cardioprotective benefits .
    <em>AD</em>012
  • HY-143888

    Angiotensin-converting Enzyme (ACE) Others
    AD013 is a dual inhibitor of cACE/NEP. AD013 is synthesized based on the previously reported C-domain selective ACE inhibitor lisinopril-tryptophan. AD013 has the potential for providing the potent antihypertensive and cardioprotective benefits .
    <em>AD</em>013
  • HY-U00005

    Reactive Oxygen Species Inflammation/Immunology
    AD 0261 is a radical scavenger which displays strong inhibitory action on the generation of lipid peroxides and superoxide anions.
    <em>AD</em> 0261
  • HY-B0579S

    Cyclosporine A-d<sub>4sub>; Ciclosporin A-d<sub>4sub>; CsA-d<sub>4sub>

    Antibiotic Complement System Phosphatase Inflammation/Immunology Cancer
    Cyclosporin A-d4 is the deuterium labeled Cyclosporin A. Cyclosporin A (Cyclosporine A) is an immunosuppressant which binds to the cyclophilin and inhibits phosphatase activity of calcineurin with an IC50 of 5 nM. Cyclosporin A also inhibits CD11a/CD18 ad
    Cyclosporin <em>A-d</em>4
  • HY-149428
    AD4
    1 Publications Verification

    PROTACs Cancer
    AD4 is an artemisinin derivative that is a proteolytic targeting chimera (PROTAC) targeting PCLAF. AD4 can effectively degrade PCLAF in RS4;11 cells (IC50: 0.6 nM), thereby activating the p21/Rb axis and exerting anti-tumor activity. AD4 also prolonged survival of RS4;11-transplanted NOD/SCID mice, with in vivo efficacy .
    <em>AD</em>4
  • HY-149853

    Sigma Receptor Neurological Disease
    AD186 is a potent and selective S1R agonist with Kis of 2.7, 27 nM for S1R and S2R, respectively. AD186 fully reverses the antiallodynic effect of BD-1063 (HY-18101A) .
    <em>AD</em>186
  • HY-W102666

    MON-4660

    Biochemical Assay Reagents Others
    AD-67 (MON-4660) is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
    <em>AD</em>-67
  • HY-105163

    MPV-2213ad

    Cytochrome P450 Endocrinology
    Finrozole (MPV-2213ad) is a nonsteroidal, orally active and competitive aromatase enzyme inhibitor. Finrozole can be used for urinary symptoms research .
    Finrozole
  • HY-B0579S1

    Cyclosporine A-d<sub>3sub>; Ciclosporin A-d<sub>3sub>; CsA-d<sub>3sub>

    Antibiotic Complement System Molecular Glues Phosphatase Others
    Cyclosporin A-d3 is the d3-labeled Cyclosporin A (HY-B0579)[1].
    Cyclosporin <em>A-d</em>3
  • HY-118561

    AD-1590

    Others Inflammation/Immunology
    Bermoprofen (AD-1590) is an orally active non-steroidal anti-inflammatory agent. Bermoprofen has potent antipyretic activities with a short biological half-life. Bermoprofen is a potent antagonist of LPS-induced fever in rabbits .
    Bermoprofen
  • HY-18507A

    RET Src Ribosomal S6 Kinase (RSK) Raf Cancer
    AD57 hydrochloride is an orally active multikinase inhibitor, inhibits RET, BRAF, S6K and Src .
    <em>AD</em>57 hydrochloride
  • HY-101963

    Raf Src Ribosomal S6 Kinase (RSK) RET Cancer
    AD80, a multikinase inhibitor, inhibits RET, RAF,SRCand S6K, with greatly reduced mTOR activity.
    <em>AD</em>80
  • HY-W011927

    Bisphenol S; Bis(4-hydroxyphenyl) sulfone

    Biochemical Assay Reagents Inflammation/Immunology
    4,4'-Sulfonyldiphenol (Bisphenol S; Bis(4-hydroxyphenyl) sulfone) is a biochemical reagent that can be used as a biological material or organic compound for life science related research .
    4,4'-Sulfonyldiphenol
  • HY-18507

    RET Raf Ribosomal S6 Kinase (RSK) Src Cancer
    AD57 is an orally active multikinase inhibitor, inhibits RET, BRAF, S6K and Src, with greatly reduces mTOR activity .
    <em>AD</em>57
  • HY-13575

    AD-5423

    5-HT Receptor Dopamine Receptor Adrenergic Receptor Sigma Receptor Neurological Disease
    Blonanserin (AD-5423) is a potent and orally active 5-HT2A (Ki=0.812 nM) and dopamine D2 receptor (Ki =0.142 nM) antagonist. Blonanserin is usually acts as an atypical antipsychotic agent and can be used for the research of extrapyramidal symptoms, excessive sedation, or hypotension .
    Blonanserin
  • HY-A0024S

    (R)-(+)-Tolterodine-d<sub>14sub> hydrochloride; (+)-Tolterodine-d<sub>14sub> hydrochloride; (R)-Tolterodine-d<sub>14sub> hydrochloride; PNU-200583-d<sub>14sub> hydrochloride

    mAChR Neurological Disease
    Tolterodine-d14 (hydrochloride) is the deuterium labeled Tolterodine hydrochloride[1]. Tolterodine hydrochloride is a potent muscarinic receptor antagonist[2][3].
    Tolterodine-d<em>14</em> hydrochloride
  • HY-136813

    Beta-secretase Amyloid-β Cholinesterase (ChE) Neurological Disease
    Multitarget AD inhibitor-1 is a selective and reversible butyrylcholinesterase (BuChE) inhibitor with IC50s of 7.22 μM and 1.55 μM for hBuChE and eqBuChE (BuChE from equine serum), respectively. Multitarget AD inhibitor-1 inhibits β-secretase (IC50hBACE-1=41.60 μM), amyloid β aggregation (IC50Aβ=3.09 μM), tau aggregation. Multitarget AD inhibitor-1, a diphenylpropylamine derivative, has the potential for multifunctional disease-modifying anti-Alzheimer’s research .
    Multitarget <em>AD</em> inhibitor-1
  • HY-R01636

    MicroRNA Cancer
    hsa-miR-548ad-3p mimics are small, chemically synthesized double-stranded RNAs that mimic endogenous miRNAs and enable miRNA functional analysis by up-regulation of miRNA activity.
    hsa-miR-548ad-3p mimic
    hsa-miR-548ad-3p mimic
  • HY-R01637

    MicroRNA Cancer
    hsa-miR-548ad-5p mimics are small, chemically synthesized double-stranded RNAs that mimic endogenous miRNAs and enable miRNA functional analysis by up-regulation of miRNA activity.
    hsa-miR-548ad-5p mimic
    hsa-miR-548ad-5p mimic
  • HY-N1150S10

    DThyd-d<sub>14sub>; NSC 21548-d<sub>14sub>

    Isotope-Labeled Compounds DNA/RNA Synthesis Endogenous Metabolite Orthopoxvirus Cancer
    Thymidine-d14 (DThyd-d14; NSC 21548-d14) is deuterium labeled Thymidine (HY-N1150). Thymidine, a specific precursor of deoxyribonucleic acid, is used as a cell synchronizing agent. Thymidine is a DNA synthesis inhibitor that can arrest cell at G1/S boundary, prior to DNA replication.
    Thymidine-d<em>14</em>
  • HY-RI01636

    MicroRNA
    hsa-miR-548ad-3p inhibitors are chemically-modified oligonucleotides that hybridize with mature miRNAs. The miRNA inhibitors have full-length nucleotide 2'-methoxy modification. The miRNA inhibitors strongly compete with mature miRNAs to prevent the complementary pairing of miRNAs and their target genes, thereby inhibiting miRNAs from functioning.
    hsa-miR-548ad-3p inhibitor
    hsa-miR-548ad-3p inhibitor
  • HY-RI01637

    MicroRNA
    hsa-miR-548ad-5p inhibitors are chemically-modified oligonucleotides that hybridize with mature miRNAs. The miRNA inhibitors have full-length nucleotide 2'-methoxy modification. The miRNA inhibitors strongly compete with mature miRNAs to prevent the complementary pairing of miRNAs and their target genes, thereby inhibiting miRNAs from functioning.
    hsa-miR-548ad-5p inhibitor
    hsa-miR-548ad-5p inhibitor
  • HY-Y0093S

    α,ω-Nonanediol-d<sub>14sub>; 1,9-Dihydroxynonane-d<sub>14sub>; Nonamethylene Glycol-d<sub>14sub>

    Isotope-Labeled Compounds Others
    NSC 5416-d14 is the deuterium labeled NSC 5416[1].
    NSC 5416-d<em>14</em>
  • HY-W013053S

    DBA-d<sub>14sub>; 1,2,5,6-Dibenzanthracene-d<sub>14sub>; Benzo[k]tetraphene-d<sub>14sub>

    Isotope-Labeled Compounds Others
    Dibenz[a,h]anthracene-d14 is the deuterium Dibenz[a,h]anthracene.
    Dibenz[a,h]anthracene-d<em>14</em>
  • HY-B0426AS2

    ALO4943A-d<sub>6sub> hydrochloride; KW4679-d<sub>6sub> hydrochloride

    Endogenous Metabolite Histamine Receptor Isotope-Labeled Compounds Inflammation/Immunology
    Olopatadine-d6 (ALO4943A-d6; KW4679-d6) hydrochloride is deuterium-labeled Olopatadine (hydrochloride) (HY-B0426A) .
    Olopatadine-d6 hydrochloride
  • HY-76569S1

    PNU-200577-d<sub>14sub>; 5-Hydroxymethyl Tolterodine-d<sub>14sub>

    mAChR Isotope-Labeled Compounds Neurological Disease
    (R)-Hydroxytolterodine-d14 is deuterated labeled Desfesoterodine (HY-76569). Desfesoterodine (PNU-200577) is a potent and selective muscarinic receptor (mAChR) antagonist with a KB and a pA2 of 0.84 nM and 9.14, respectively . Desfesoterodine is a major pharmacologically active metabolite of Tolterodine (PNU-200583; HY-A0024) and Fesoterodine (HY-70053) . Desfesoterodine improves cerebral infarction induced detrusor overactivity in rats .
    (R)-Hydroxytolterodine-d<em>14</em>
  • HY-R01636A

    MicroRNA
    hsa-miR-548ad-3p agomirs are chemically-modified double-strand miRNA mimics with modified mature miRNA strand: 2 phosphorothioates at the 5' end, 4 phosphorothioates at the 3' end, 3' end cholesterol group, and full-length nucleotide 2'-methoxy modification. They are designed to mimic endogenous miRNAs and recommended for miRNA functional studies. Compared with miRNA mimics, they exhibits enhanced cellular uptake, stability and regulatory activity in vivo.
    hsa-miR-548ad-3p agomir
    hsa-miR-548ad-3p agomir

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