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Unnatural

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20

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4

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1

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Natural
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10

Click Chemistry

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-139014
    N-ε-propargyloxycarbonyl-L-lysine
    1 Publications Verification

    H-​L-​Lys(Poc)​-​OH

    Fluorescent Dye Cancer
    N-ε-propargyloxycarbonyl-L-lysine (H-L-Lys(Poc)-OH) is a lysine-based unnatural amino acid (UAA). N-ε-propargyloxycarbonyl-L-lysine is widely used for bio-conjugation of fluorescent probes in diverse organisms from E. coli to mammalian cells even in animals . N-ε-propargyloxycarbonyl-L-lysine is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    N-ε-propargyloxycarbonyl-L-lysine
  • HY-B1258

    Aminomethylbenzoic acid; α-Amino-p-toluic acid

    Amino Acid Derivatives Others
    4-(Aminomethyl)benzoic acid is an unnatural amino acid derivative and an antifibrinolytic drug.
    4-(Aminomethyl)benzoic acid
  • HY-101937B

    Fluorescent Dye Others
    L-ANAP hydrochloride is a genetically encodable and polarity-sensitive fluorescent unnatural amino acid (Uaa).
    L-ANAP hydrochloride
  • HY-101937C
    (±)-ANAP hydrochloride
    1 Publications Verification

    Fluorescent Dye Others
    (±)-ANAP hydrochloride is the unnatural amino acid analog of prodan, acts as a fluorescent probes, and enhances environmental sensitivity.
    (±)-ANAP hydrochloride
  • HY-126069

    15(R)-Ciloprost; 15(R)-ZK 36374

    Others Others
    15(R)-Iloprost is the unnatural or inverted C-15 epimer of lloprost (HY-A0096) .
    15(R)-Iloprost
  • HY-101937A

    Fluorescent Dye Others
    (±)-ANAP is the unnatural amino acid analog of prodan, acts as a fluorescent probes, and enhances environmental sensitivity.
    (±)-ANAP
  • HY-101937

    Fluorescent Dye Others
    L-ANAP is a genetically encodable and polarity-sensitive fluorescent unnatural amino acid (Uaa) .
    L-ANAP
  • HY-101937D

    Fluorescent Dye Others
    L-ANAP TFA is a genetically encodable and polarity-sensitive fluorescent unnatural amino acid (Uaa) .
    L-ANAP TFA
  • HY-W016443

    Others Neurological Disease Inflammation/Immunology
    L-m-Tyrosine is an unnatural amino acid, that has potential in the research of Parkinsons disease, Alzheimers disease, and arthritis .
    L-m-Tyrosine
  • HY-100217

    Amino Acid Derivatives Others
    DL-3-Indolylglycine is an unnatural amino acid that is very similar to Tryptophan, with the indole moiety directly attached to the α-position.
    DL-3-Indolylglycine
  • HY-W002272

    Nucleoside Antimetabolite/Analog Others
    Isocytosine is a non-natural nucleobase and an isomer of cytosine. It is used in combination with Isoguanine in studies of unnatural nucleic acid analogues of the normal base pairs in DNA and used as a nucleobase of hachimoji RNA .
    Isocytosine
  • HY-163485

    Androgen Receptor Endocrinology
    AR antagonist 8 (compound 16) is a potent Lupeol-inspired androgen receptor (AR) antagonist with an IC50 of 0.76 μM. AR antagonist 8 is a uniquely substituted unnatural entestrane .
    AR antagonist 8
  • HY-151693A

    ADC Linker Others
    H-L-Tyr(2-azidoethyl)-OH is a unnatural Tyrosine derivative. H-L-Tyr(2-azidoethyl)-OH is a click chemistry reagent containing an azide group .
    H-L-Tyr(2-azidoethyl)-OH
  • HY-151693

    ADC Linker Others
    H-L-Tyr(2-azidoethyl)-OH hydrochloride is a unnatural Tyrosine derivative. H-L-Tyr(2-azidoethyl)-OH hydrochloride is a click chemistry reagent containing an azide group .
    H-L-Tyr(2-azidoethyl)-OH hydrochloride
  • HY-W002299

    Boc-D-Leu-OH hydrate

    Amino Acid Derivatives Neurological Disease
    Boc-D-Leucine monohydrate (Boc-D-Leu-OH hydrate) is an N-Boc-protected form of D-Leucine (L330150). D-Leucine is an unnatural isomer of L-Leucine (L330110) that acts as an auto-inhibitor of lactic streptococci. D-Leucine shows potent anti-seizure effect .
    Boc-D-Leucine monohydrate
  • HY-13859

    L-FMAU

    HBV DNA/RNA Synthesis Orthopoxvirus Infection
    Clevudine (L-FMAU), a nucleoside analog of the unnatural L-configuration, has potent anti-HBV activity with long half-life, low toxicity. Clevudine is a non-competitive inhibitor that is not incorporated into the viral DNA but rather binds to the polymerase. Clevudine is active against cowpox virus respiratory infection in mice .
    Clevudine
  • HY-114862

    13,14-dihydro-15(R)-PGE1

    Endogenous Metabolite Others
    13,14-dihydro-15(R)-Prostaglandin E1 (13,14-dihydro-15(R)- PGE1) is an analog of 13,14-dihydro- PGE1 which has the hydroxyl group at C-15 in the unnatural R configuration .
    13,14-dihydro-15(R)-Prostaglandin E1
  • HY-151687

    ADC Linker Others
    Fmoc-L-Tyr(2-azidoethyl)-OH is a click chemistry reagent containing an azide group. Fmoc-L-Tyr(2-azidoethyl)-OH is unnatural Fmoc-protected Tyrosine derivative bears an azidoethyl substitution as reactive handle e.g. for biorthogonal conjugations, via a Cu(I)-catalyzed 1,3-dipolar Click cycloaddition with alkynes. And azido-UAAs can be employed as IR reporters .
    Fmoc-L-Tyr(2-azidoethyl)-OH
  • HY-128676

    H-​L-​Lys(Poc)​-​OH hydrochloride

    Amino Acid Derivatives Cancer
    N-ε-propargyloxycarbonyl-L-lysine (H-L-Lys(Poc)-OH) hydrochloride is a lysine-based unnatural amino acid (UAA). N-ε-propargyloxycarbonyl-L-lysine is widely used for bio-conjugation of fluorescent probes in diverse organisms from E. coli to mammalian cells even in animals . N-ε-propargyloxycarbonyl-L-lysine (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.
    N-ε-propargyloxycarbonyl-L-lysine hydrochloride
  • HY-139121

    15-epi Bimatoprost free acid; 15(R)-Bimatoprost free acid; 15(R)-17-phenyl trinor PGF2α

    Prostaglandin Receptor Endocrinology
    17-phenyl trinor Prostaglandin F2α (17-phenyl trinor PGF2α) N-ethyl amide is an F-series prostaglandin analog which has been approved for use as an ocular hypotensive agent. Investigations in our lab have shown that 17-phenyl trinor PGF2α ethyl amide is converted by an amidase enzymatic activity in the human cornea to yield the corresponding free acid, with a conversion rate of about 25 μg/cornea/24 hr. The free acid, 17-phenyl trinor PGF2α, is a potent FP receptor agonist. 15(R)-17-phenyl trinor PGF2α is the 15-epi, or “unnatural” isomer of this active free acid metabolite. It has much diminished FP receptor-mediated activity, which is generally 1.5 to 2 logs less than the 15(S)-isomer. In human and animal models of glaucoma, FP receptor agonist activity corresponds very closely with intraocular hypotensive activity.
    15(R)-17-Phenyl trinor Prostaglandin F2α

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