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Results for "

USP1

" in MedChemExpress (MCE) Product Catalog:

15

Inhibitors & Agonists

1

Natural
Products

1

Isotope-Labeled Compounds

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-145471
    KSQ-4279
    1 Publications Verification

    USP1-IN-1

    		 Deubiquitinase Apoptosis Cancer
    KSQ-4279 (USP1-IN-1) is a potent, first-in-class, and highly selective USP1 inhibitor. KSQ-4279 shows anticancer effects [1].
    KSQ-4279
  • HY-148099
    USP1-IN-2

    		Deubiquitinase Cancer
    USP1-IN-2 (Compound I-193) is a potent ubiquitin-specific protease 1 (USP1) inhibitor with an IC50 of less than about 50 nM [1].
    <em>USP1</em>-IN-2
  • HY-RS15520
    USP1 Human Pre-designed siRNA Set A

    		Small Interfering RNA (siRNA) Others

    USP1 Human Pre-designed siRNA Set A contains three designed siRNAs for USP1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    USP1 Human Pre-designed siRNA Set A
    USP1 Human Pre-designed siRNA Set A
  • HY-148184
    USP1-IN-3

    		Deubiquitinase Cancer
    USP1-IN-3 is a selective USPI inhibitor. USP1-IN-3 inhibits USPI-UAFI with an IC50 value of ＜30 nM. USP1-IN-3 can be used for the research of cancer [1].
    <em>USP1</em>-IN-3
  • HY-153731
    USP1-IN-4

    		Deubiquitinase Cancer
    USP1-IN-4 (compound 10) is an effective USP1 inhibitor with an IC50 value of 2.44 nM. USP1-IN-4 has anticancer activity and synergistic activity with various anticancer drugs [1].
    <em>USP1</em>-IN-4
  • HY-156525
    USP1-IN-6

    		Deubiquitinase Cancer
    USP1-IN-6 (compound 11) is a USP1 inhibitor (IC50<50 nM). USP1-IN-5 also inhibits MDA-MB-436 cells with IC50 <50 nM [1].
    <em>USP1</em>-IN-6
  • HY-156524
    USP1-IN-5

    		Deubiquitinase Cancer
    USP1-IN-5 (compound 10) is a USP1 inhibitor (IC50<50 nM). USP1-IN-5 also inhibits MDA-MB-436 cells with IC50 <50 nM [1].
    <em>USP1</em>-IN-5
  • HY-161446
    USP1-IN-7

    		Deubiquitinase Cancer
    USP1-IN-7 (Compound 3) is an inhibitor for ubiquitin specific peptidase 1 (USP1) and its cofactor UAF1, with IC50 ≤50 nM. USP1-IN-7 inhibits proliferation of MDA-MB-436 with IC50 ≤50 nM [1].
    <em>USP1</em>-IN-7
  • HY-161447
    USP1-IN-8

    		Deubiquitinase Cancer
    USP1-IN-8 (Compound 16) is an inhibitor for ubiquitin specific peptidase 1 (USP1) and its cofactor UAF1, with IC50 ≤50 nM. USP1-IN-8 inhibits proliferation of MDA-MB-436 with IC50 ≤50 nM [1].
    <em>USP1</em>-IN-8
  • HY-153365
    I-138

    		Deubiquitinase Cancer
    I-138 is an orally active, reversible inhibitor of USP1-UAF1 (IC50: 4.1 nM; Ki: 5.4 nM), structurally related to ML323 (HY-17543). I-138 induces monoubiquitination of FANCD2 and PCNA in cells and eliminates USP1 autocleavage in cells [1].
    I-138
  • HY-15757
    SJB2-043
    3 Publications Verification

    		 Deubiquitinase Cancer
    SJB2-043 is an inhibitor of the native USP1/UAF1 complex with IC50 of 544 nM.
    SJB2-043
  • HY-12988
    C527
    1 Publications Verification
    C527 is a is a pan DUB enzyme inhibitor, with a high potency for the USP1/UAF1 complex (IC50=0.88 μM).
    C527
  • HY-17543
    ML-323
    Maximum Cited Publications
    11 Publications Verification

    		 Deubiquitinase Cancer
    ML-323 is a reversible, potent USP1-UAF1 inhibitor with IC50 of 76 nM in a Ub-Rho assay. The measured inhibition constants of ML-323 for the free enzyme (Ki) is 68 nM.
    ML-323
  • HY-80012
    SJB3-019A
    5+ Cited Publications

    		 Deubiquitinase Cancer
    SJB3-019A is a potent and novel USP1 inhibitor, 5 times more potent than SJB2-043 in promoting ID1 degradation and cytoxicity in K562 cells with IC50 of 0.0781 μM.
    SJB3-019A
  • HY-N6979
    Crustecdysone
    4 Publications Verification

    20-Hydroxyecdysone

    		 Caspase Autophagy Endogenous Metabolite Cardiovascular Disease
    Crustecdysone (20-Hydroxyecdysone) is a naturally occurring ecdysteroid hormone isolated from Serratula coronata which controls the ecdysis (moulting) and metamorphosis of arthropods, it inhibits caspase activity and induces autophagy via the 20E nuclear receptor complex, EcR-USP . Crustecdysone exhibits regulatory or protective roles in the cardiovascular system . Crustecdysone is an active metabolite of Ecdysone (HY-N0179) .
    Crustecdysone

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