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Chemicals & Small Molecules

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    Results for Chemicals & Small Molecules ( 98424 )

      • Fluvastatin-d6 Sodium Salt

        Ref: TMIH-0242
        Sizes: 1 mg, 5 mg, 10 mg

        Fluvastatin-d6 Sodium Salt is a deuterated compound of Fluvastatin Sodium Salt. Fluvastatin Sodium Salt has a CAS number of 93957-55-2. Fluvastatin sodium, a competitive inhibitor of hydroxymethylglutaryl-coenzyme A reductase (HMGCR), is a commonly used cholesterol lowering agent.

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      • Folic Acid-d4

        Ref: TMIH-0243
        Sizes: 500 μg

        Folic Acid-d4 is a deuterated compound of Folic Acid.

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      • Fomesafen-d3

        Ref: TMIH-0244
        Sizes: 1 mg, 5 mg, 25 mg, 10 mg

        Fomesafen-d3 is a deuterated compound of Fomesafen. Fomesafen has a CAS number of 72178-02-0. Fomesafen is a diphenyl ether herbicide and an inhibitor of efficient and selective protoporphyrinogen IX oxidase (PPO).

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      • Formoterol-d6

        Ref: TMIH-0245
        Sizes: 1 mg, 5 mg, 25 mg, 10 mg

        Formoterol-d6 is a deuterated compound of Formoterol. Formoterol has a CAS number of 128954-45-0.

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      • Formoterol-d6 Fumarate

        Ref: TMIH-0246
        Sizes: 1 mg, 5 mg, 25 mg, 10 mg

        Formoterol-d6 Fumarate is a deuterated compound of Formoterol Fumarate. Formoterol Fumarate has a CAS number of 169375-55-7.

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      • Furfuryl-d5-amine HCl

        Ref: TMIH-0247
        Sizes: 25 mg, 50 mg, 10 mg

        Furfuryl-d5-amine HCl is a deuterated compound of Furfuryl-amine HCl. Furfuryl-amine HCl has a CAS number of 1219799-26-4.

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      • Furosemide-d5

        Ref: TMIH-0248
        Sizes: 1 mg, 5 mg, 10 mg

        Furosemide-d5 is a deuterated compound of Furosemide.

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      • Galantamin-d6

        Ref: TMIH-0249
        Sizes: 1 mg, 5 mg, 10 mg

        Galantamin-d6 is a deuterated compound of Galantamin.

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      • Gefapixant-d3

        Ref: TMIH-0250
        Sizes: 1 mg, 5 mg, 25 mg, 10 mg

        Gefapixant-d3 is a deuterated compound of Gefapixant. Gefapixant has a CAS number of 1015787-98-0. Gefapixant is a P2X3 receptor (P2X3R) antagonist with IC50 of ~30 nM at recombinant hP2X3 homotrimers and 100-250 nM at hP2X2/3 heterotrimeric receptors.

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