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 (60498):

Cat. No. Product Name CAS No. Purity Chemical Structure
  • HY-125830
    ITIC 1664293-06-4 98%
    ITIC, non-fullerene acceptor, is an indacenodithienothiophene-based postfullerene electron acceptor, crystallizes in a profoundly different way as compared to fullerenes. ITIC has a superior thermal stability and undergoes a glass-crystal transition considerably below its high Tg of 180 °C.
    ITIC
  • HY-126106
    (BrMT)2 622011-16-9 98%
    (BrMT)2 (compound 2) is a non-peptide snail toxin that slows down the activation of Kv1.1 channels.
    (BrMT)2
  • HY-126171
    Hypusine 34994-11-1 98%
    Hypusine is a natural amino acid. The post-translational synthesis of hypusine is mainly catalyzed by deoxyhypusine synthase (DHPS) and deoxyhypusine hydroxylase (DOHH).
    Hypusine
  • HY-126176
    Cloransulam-methyl 147150-35-4 98%
    Cloransulam-methyl is a triazolopyrimidine sulfonanilide herbicide. Cloransulam-methyl can be used to control broadleaf weeds in soybean by acetolactate synthase (ALS) inhibition.
    Cloransulam-methyl
  • HY-126194
    Tolcapone 3-β-D-glucuronide 204853-33-8 98%
    Tolcapone 3-β-D-glucuronide (Ro 61-1448) is an O-methyl metabolite and the glucuronide metabolite of Tolcapone (Ro 40-7592; HY-17406). Tolcapone 3-β-D-glucuronide is pharmacologically inactive.
    Tolcapone 3-β-D-glucuronide
  • HY-126199
    Tetrachlorvinphos 22248-79-9 98%
    Tetrachlorvinphos is an organophosphorus pesticide that has the activity of inhibiting cholinesterase. Tetrachlorvinphos is used as a pesticide, mainly for the control of pests. Tetrachlorvinphos has low toxicity to mammals.
    Tetrachlorvinphos
  • HY-12625A
    MIV-6R 1560968-55-9 98%
    MIV-6R is an optimized small molecule inhibitor of menin-mixed lineage leukemia (MLL) interaction with IC50 = 56 nM, and its specific mechanism of action activity has been validated in MLL leukemia cells.
    MIV-6R
  • HY-126365
    Alisol B acetate 19865-76-0 98%
    Alisol B acetate is a Triterpenoids product that can be isolated from the tubers of Alisma plantago-aquatica Linn..
    Alisol B acetate
  • HY-126476
    Justicisaponin I 79162-16-6 98%
    Justicisaponin I can be used as an anti-fertility agent. Justicisaponin I stabilizes the acrosome membrane of sperm, and inhibits the release of acid hydrolase and sperm proteins.
    Justicisaponin I
  • HY-126484
    Eremofortin B 60048-73-9 98%
    Eremofortin B is a sesquiterpenoid compound synthesized by penicillium roqueforti PR Toxin (PRT).
    Eremofortin B
  • HY-126574
    Pantothenoylcysteine 13147-34-7 98%
    Pantothenoylcysteine is the biosynthetic precursor of CoA. Pantothenoylcysteine can be used to study microbial metabolism.
    Pantothenoylcysteine
  • HY-126646
    Sporeamicin A 131418-65-0 98%
    Sporeamicin A is an active compound.
    Sporeamicin A
  • HY-126655
    Yunnanxane 139713-81-8 98%
    Yunnanxane (compound 1) is a taxane diterpenoid that can be found in Taxus chinensis var..
    Yunnanxane
  • HY-126703
    Lantanose A 145204-38-2 98%
    Lantanose A is an oligosaccharide, which can be isolated from the root of Lantana camara.
    Lantanose A
  • HY-126723
    Proline cetyl ester 97010-18-9 98%
    Proline cetyl ester is an amnesic-inducing compound that can induce profound amnesia in rats, and its amnesic effect can be abolished by piracetam.
    Proline cetyl ester
  • HY-126725
    Chitinovorin B 95722-76-2 98%
    Chitinovorin B is an active compound.
    Chitinovorin B
  • HY-126748
    VUF14862 2223023-78-5 98%
    VUF14862 is a stable and fatigue-resistant photoswitchable GPCR antagonist targeting the histamine H3 receptor (H3R) pathway. VUF14862 binds to H3R with >10-fold increased affinity upon 360 nm irradiation. VUF14862 can be used for spatiotemporal studies of H3R signaling.
    VUF14862
  • HY-126753
    Kujimycin A 33955-27-0 98%
    Kujimycin A is an active compound.
    Kujimycin A
  • HY-126801
    Sannamycin A 72503-79-8 98%
    Sannamycin A is an active compound.
    Sannamycin A
  • HY-126822
    MDL27324 123285-50-7 98%
    MDL27324 is an inhibitor of neutrophil proteases. MDL27324 can be taken up by the cell and has a modest inhibitory effect on the proteolysis of ingested fluoresceinated immune complexes (200 μM, 20% inhibition).
    MDL27324