1. Others

Others

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

Others Related Products (73874):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-118836
    GSK215083 607742-80-3 98%
    GSK215083 is a high affinity 5-HT6 receptor antagonist. GSK215083 can serves as a promising 5-HT6 radioligand candidate by radiolabeled with (11)C via methylation.
    GSK215083
  • HY-118851
    NSC-77053 77308-57-7 98%
    NSC-77053 is a potent BoNT/E inhibitor with an IC50 and a Ki of 2.4 μM and 1.29 μM, respectively.
    NSC-77053
  • HY-118853
    Dichlofenthion 97-17-6 98%
    Dichlofenthion is an organophosphorus (OP) pesticide. Dichlofenthion can be for the control of sheep maggot fly.
    Dichlofenthion
  • HY-118854
    Fepradinol 36981-91-6 98%
    Fepradinol is an active compound.
    Fepradinol
  • HY-118896S
    Acequinocyl-d25 2469735-25-7 98%
    Acequinocyl-d25 is the deuterium labeled Acequinocyl.
    Acequinocyl-d25
  • HY-118902
    Aloisine B 496864-14-3 98%
    Aloisine B (compound 9) is a cyclin-dependent kinase (CDK) inhibitor. Aloisine B inhibits cell proliferation by arresting cells in both G1 and G2 via competing with ATP-binding pocket.
    Aloisine B
  • HY-118919
    CYM5181 695155-81-8 98%
    CYM5181 is a novel S1P1 agonist with a pEC50 value of -8.47.
    CYM5181
  • HY-118923R
    Saflufenacil (Standard) 372137-35-4
    Saflufenacil (Standard) is the analytical standard of Saflufenacil. This product is intended for research and analytical applications. Saflufenacil is a herbicide of the pyrimidinedione chemical class preplant burndown and selective preemergence dicot weed control in multiple crops, including corn. Saflufenacil is a potent inhibitor of protoporphyrinogen IX oxidase (PPO).
    Saflufenacil (Standard)
  • HY-118955
    Acid red 88 1658-56-6 98%
    Acid red 88 is a biochemical reagent.
    Acid red 88
  • HY-118964
    Tyrphostin AG 568 151013-48-8 98%
    Tyrphostin AG 568 is a tyrphostin tyrosine kinase inhibitor that induces erythroid differentiation. Tyrphostin AG 568 can be utilized in research related to autologous bone marrow transplantation.
    Tyrphostin AG 568
  • HY-119002
    BO-1236 105358-77-8 98%
    BO-1236 is a compound with antibacterial activity. It has strong activity against Gram-negative bacteria including Pseudomonas aeruginosa. It has shown activity superior to or equivalent to that of some commonly used antibiotics in in vitro and in vivo experiments, and has a certain stability against β-lactamase.
    BO-1236
  • HY-119012
    L 681217 93522-10-2 98%
    L 681217 is an active compound.
    L 681217
  • HY-119055
    Sch 33303 89108-58-7 98%
    Sch 33303 is an orally active antiallergy agent that inhibits the release of the sulfidopeptide leukotrienes. Sch 33303 is promising for research of asthma.
    Sch 33303
  • HY-119082
    (E/Z)-VU0029767 326001-01-8 98%
    (E/Z)-VU0029767 is an allosteric enhancer of M1 muscarinic receptors with the activity to modulate M1 receptor activity. (E/Z)-VU0029767 can enhance M1 receptor activity by increasing agonist affinity, but exhibits different properties from other compounds under different experimental conditions, such as effects on mutant M1 receptors and effects on downstream signaling pathways.
    (E/Z)-VU0029767
  • HY-119082A
    VU0029767 1134973-88-8 98%
    VU0029767 is an allosteric enhancer of the M1 muscarinic receptor with the activity to modulate M1 receptor activity. VU0029767 can enhance M1 receptor activity by increasing agonist affinity, but exhibits different properties from other compounds under different experimental conditions, such as effects on mutant M1 receptors and effects on downstream signaling pathways.
    VU0029767
  • HY-119088
    Estrogen receptor modulator 12 554431-74-2 98%
    Estrogen receptor modulator 12 (compound 1a-(R)) is a selective estrogen receptor modulator with estrogen agonist and antagonist activities in in vivo models. Estrogen receptor modulator 12 exhibits antagonist effects on the uterus and estrogen agonist activities on bone, plasma lipids, hot flashes, and vagina in in vivo models, and is a potential compound for suppressing postmenopausal symptoms.
    Estrogen receptor modulator 12
  • HY-119130
    SQ 28516 92121-46-5 98%
    SQ 28516 is an active compound.
    SQ 28516
  • HY-119136
    BFF-122 1152314-49-2 98%
    BFF-122 is a compound that selectively inhibits mammalian kynurenine aminotransferase II.
    BFF-122
  • HY-119140
    LY 116467 57202-76-3 98%
    LY 116467 is an active compound.
    LY 116467
  • HY-119148
    SQ 28517 92131-67-4 98%
    SQ 28517 is an active compound.
    SQ 28517