2. Others

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Others

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There are a number of inhibitors, agonists, and antagonists which we cannot make precise classification because the research area is still unknown.

Others Verwandte Produkte (73744):

Art. -Nr. Produktname CAS. Nr. Reinheit Chemische Struktur
  • HY-137530
    8-MA-cAMP 33823-18-6 98%
    8-MA-cAMP (8-Methylamino-cAMP) is a cyclic AMP analog that acts as a site-selective PKA agonist with similar affinity for the B site of type I and type II protein kinase A. 8-MA-cAMP is used in conjunction with priming analogs that show site A preference, such as 8-piperidinyl cAMP, to achieve selective stimulation of type I.
    8-MA-cAMP
  • HY-137540
    Phenyl-1-thio-β-D-glucopyranoside 2936-70-1 98%
    Phenyl-1-thio-β-D-glucopyranoside can be used in glycobiology research.
    Phenyl-1-thio-β-D-glucopyranoside
  • HY-137575
    Terbutalone 139508-58-0 98%
    Terbutalone is a derivative of Terbutaline (HY-B0802A). Terbutaline is an orally active β2-adrenergic receptor agonist and an active metabolite of Bambuterol (HY-17501). Terbutaline can be used in asthma symptom research.
    Terbutalone
  • HY-137581
    Terbinafine impurity 13 162227-14-7 98%
    Terbinafine impurity 13 is an impurity of Terbinafine.
    Terbinafine impurity 13
  • HY-137602
    P1,P2-Diuridine-5’-diphosphate 26184-65-6 98%
    P1,P2-Diuridine-5’-diphosphate (Up2U) is a symmetrical dinucleoside polyphosphate containing two pyrimidine base moieties. P1,P2-Diuridine-5’-diphosphate is also an activator of purinergic P2Y receptor.
    P1,P2-Diuridine-5’-diphosphate
  • HY-137618
    Sp-dGTPαS 80902-28-9 98%
    Sp-dGDPαS is a regulator of GDP-binding proteins. Sp-dGDPαS is metabolically more stable than GTP.
    Sp-dGTPαS
  • HY-137619
    Sp-dCTPαS 80951-75-3 98%
    Sp-dCTPαS is a regulator of CTP-binding proteins. Sp-dCTPαS is metabolically more stable than CTP.
    Sp-dCTPαS
  • HY-137620
    Sp-dATPαS 80875-87-2 98%
    Sp-dADPαS is a regulator of ADP-binding proteins. Sp-dADPαS is metabolically more stable than ATP.
    Sp-dATPαS
  • HY-137623
    Sp-cCMPS 87063-81-8 98%
    Sp-cCMPS is a cCMP analog that activates the binding protein of cCMP.
    Sp-cCMPS
  • HY-137624
    Sp-cAMPS-AM 1037535-49-1 98%
    Sp-cAMPS-AM is an analog of cAMP. Sp-cAMPS-AM acts as the inducer of PKA activation and CREB phosphorylation, through entrance into the cell and release of its parent polar structure Sp-cAMPS.
    Sp-cAMPS-AM
  • HY-137626
    Sp-ATPαS 58976-48-0 98%
    Sp-ATPαS is a regulator of ATP-binding proteins. Sp-ATPαS is a competitive antagonist of the human P2Y1 receptor, which can inhibit the calcium signal induced by ADP. Sp-ATPαS is metabolically more stable than ATP. Sp-ATPαS can be used to study the binding patterns of metals and nucleotides in enzymatic reactions.
    Sp-ATPαS
  • HY-137627
    Sp-ADPαS 59286-20-3 98%
    Sp-ADPαS is a regulator of ADP-binding proteins. Sp-ADPαS is metabolically more stable than ADP.
    Sp-ADPαS
  • HY-137640
    Sp-8-Br-cAMPS 127634-20-2 98%
    Sp-8-Br-cAMPS is an analog of cAMP(HY-B1511). Sp-8-Br-cAMPS is an agonist for cAMP, which performs a protein kinase A (PKA) activating activity with EC50 of 360 nM. Sp-8-Br-cAMPS inhibits proliferation of T cells and the haemocyte non-self response in Lepidoptera larve.
    Sp-8-Br-cAMPS
  • HY-13766A
    Timcodar mesylate 183313-30-6 98%
    Timcodar mesylate (VX-853-2) and its analog VX-710 are mammalian multidrug-resistant bacterial efflux pump inhibitors that directly inhibit ethidium bromide efflux in Staphylococcus aureus. Timcodar mesylate has the potential to enhance antibiotic activity by inhibiting bacterial efflux pumps, effectively reducing the minimum inhibitory concentration of some antibiotics against Gram-positive pathogens such as Staphylococcus aureus, Enterococcus and Streptococcus pneumoniae.
    Timcodar mesylate
  • HY-137673
    2'-Deoxy-NAD+ 6697-37-6 98%
    2'-Deoxy-NAD+ is a noncompetitive inhibitor for NAD+ with a Ki of 32 μM. 2'-Deoxy-NAD+ can be utilized as a substrate to study the ADP-ribosyl transfer reaction.
    2'-Deoxy-NAD+
  • HY-137701
    ddATPαS 112820-39-0 98%
    ddATPαS is a dideoxynucleotide that can be used for DNA sequencing.
    ddATPαS
  • HY-137704
    2′-Deoxy-ADPR 111864-49-4 98%
    2′-Deoxy-ADPR is an agonist for transient receptor potential melastatin 2 channel (TRPM2 channel). 2′-Deoxy-ADPR may acts as the signaling molecule in Jurkat T-lymphocytes.
    2′-Deoxy-ADPR
  • HY-137768
    Captopril EP Impurity B 80629-35-2 98%
    Captopril EP Impurity B is an impurity of Captopril. Captopril (SQ-14534), antihypertensive agent, is a thiol-containing competitive, orally active angiotensin-converting enzyme (ACE) inhibitor (IC50=0.025 μM).
    Captopril EP Impurity B
  • HY-137769
    Captopril EP Impurity C 26473-47-2 98.0%
    Captopril EP Impurity C is an impurity of Captopril. Captopril (SQ-14534), antihypertensive agent, is a thiol-containing competitive, orally active angiotensin-converting enzyme (ACE) inhibitor (IC50=0.025 μM).
    Captopril EP Impurity C
  • HY-137772
    Captopril EP Impurity E 23500-15-4 98%
    Captopril EP Impurity E is an impurity of Captopril. Captopril (SQ-14534), antihypertensive agent, is a thiol-containing competitive, orally active angiotensin-converting enzyme (ACE) inhibitor (IC50=0.025 μM).
    Captopril EP Impurity E