Outros inibidores
Esta categoria abrange uma ampla variedade de inibidores que não se encaixam nas classificações padrão, mas que ainda são essenciais para várias pesquisas bioquímicas e farmacológicas. Esses inibidores podem direcionar vias, enzimas e interações moleculares únicas ou menos estudadas, fornecendo ferramentas valiosas para áreas de pesquisa especializadas. Na CymitQuimica, oferecemos uma seleção diversificada de inibidores de alta qualidade que abrangem múltiplos alvos biológicos e disciplinas de pesquisa, permitindo que você explore novas vias terapêuticas e aprofunde sua compreensão de processos biológicos complexos.
Foram encontrados 37926 produtos de "Outros inibidores"
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
SARS-CoV-2 nsp14-IN-2
<p>SARS-CoV-2 nsp14-IN-2: Strong Nsp14 methyltransferase inhibitor (IC50: 0.09 μM), potential for COVID-19 research.</p>Fórmula:C21H21N5O5SCor e Forma:SolidPeso molecular:455.49GNTI TFA
CAS:<p>GNTI TFA is a selective kappa opioid receptor antagonist.</p>Fórmula:C31H31F6N5O7Cor e Forma:SolidPeso molecular:699.60Trk-IN-8
<p>Trk-IN-8: TRK inhibitor with IC50 of 0.42 nM (TRKA), 0.89 nM (TRKA-G595R), 1.5 nM (TRKC-G623R).</p>Fórmula:C18H16F2N6O2Cor e Forma:SolidPeso molecular:386.36Acetoxycycloheximide
CAS:<p>Acetoxycycloheximide triggers TNF receptor 1, prompts apoptosis, and cytochrome c release by activating c-Jun N-terminal kinase.</p>Fórmula:C17H25NO6Cor e Forma:SolidPeso molecular:339.38ROS1-IN-1
<p>ROS1-IN-1, a potent ROS1 kinase inhibitor, has an IC50 of 0.097 μM.</p>Fórmula:C17H15ClN6SCor e Forma:SolidPeso molecular:370.86PTP1B-IN-18
<p>PTP1B-IN-18 is an orally active, fully mixed protein tyrosine phosphatase 1B (PTP1B) inhibitor (Ki: 35.2 μM).PTP1B-IN-18 can be used to study type 2 diabetes.</p>Fórmula:C26H19N3O4SCor e Forma:SolidPeso molecular:469.51CGS 22652
CAS:<p>CGS 22652 has thromboxane receptor antagonism combined with thromboxane synthase inhibition.</p>Fórmula:C22H29ClN2O4SCor e Forma:SolidPeso molecular:452.99Dexnebivolol
CAS:<p>Dexnebivolol (R67138), a ß-adrenergic antagonist, is Nebivolol's enantiomer with β1 blocking and vasodilation properties.</p>Fórmula:C22H25F2NO4Cor e Forma:SolidPeso molecular:405.43ZK-Thiazolidinone
CAS:<p>ZK-Thiazolidinone (TAL), ATP-competitive PLK1 inhibitor, disrupts cell division processes in vitro and in vivo, targeting human/mouse tumors.</p>Fórmula:C23H26F3N5O2SCor e Forma:SolidPeso molecular:493.55Anti-inflammatory agent 23
<p>Anti-inflammatory agent 23 blocks LPS-induced NO (IC50: 0.449 μM) and binds p65 well.</p>Fórmula:C34H49NO6Cor e Forma:SolidPeso molecular:567.76SARS 3CLpro-IN-1
CAS:<p>SARS 3CLpro-IN-1: stereospecific SARS 3CL protease inhibitor, octahydroisochromene class, IC50 = 95 μM.</p>Fórmula:C22H38N4O2Cor e Forma:SolidPeso molecular:390.56ER Thermo Yellow
CAS:<p>ER Thermo Yellow is a high-sensitivity (3.9%/°C) fluorescent probe designed for temperature visualization specifically targeting the endoplasmic reticulum.</p>Fórmula:C27H20BClF5N3O3Peso molecular:575.72Tezampanel hydrate
CAS:<p>Tezampanel is used for the treatment of migraine, neuropathic pain.</p>Fórmula:C13H23N5O3Cor e Forma:SolidPeso molecular:297.35FCE-24379
CAS:<p>FCE-24379 is a selective antagonist of vascular serotonin receptors that has been shown to lowers blood pressure in hypertensive rats.</p>Fórmula:C20H22N4O2Cor e Forma:SolidPeso molecular:350.41UNC7467
CAS:<p>UNC7467, potent IP6K2/1/6 inhibitor (4.9/8.9/1320 nM); lowers inositol pyrophosphates, minimal impact on other inositol phosphates; for obesity research.</p>Fórmula:C20H13NO3Pureza:98.28% - 98.64%Cor e Forma:SoildPeso molecular:315.32Antitumor agent-65
CAS:<p>Antitumor agent-65 (Compound 5) is an analogue/derivative of (-)-cleistenolide. Antitumor agent-65 has potential in cancer research.</p>Fórmula:C18H17NO10Cor e Forma:SolidPeso molecular:407.33Gentamicin C1
CAS:<p>Gentamicin C1 is a broad-spectrum aminoglycoside antibiotic with antibacterial activity.</p>Fórmula:C21H43N5O7Cor e Forma:SolidPeso molecular:477.595Naphthablin
CAS:<p>Naphthablin is a naphthoquinone compound that inhibits the function of the Abl oncogene. It prevents the morphological transformation of v-ablts-NIH3T3 cells induced by Abl and also suppresses RNA synthesis.</p>Fórmula:C29H36O8Cor e Forma:SolidPeso molecular:512.591Isoleucyl tRNA synthetase-IN-1
CAS:<p>Isoleucyl tRNA synthetase-IN-1 is a selective and potent inhibitor (Ki: 88 nM) that targets isoleucyl tRNA synthetase (IleRS).</p>Fórmula:C23H35N5O7SCor e Forma:SolidPeso molecular:525.62Sannamycin K
CAS:<p>Sannamycin K is an aminoglycoside antibiotic with weak antibacterial activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C13H26N4O4Cor e Forma:SolidPeso molecular:302.37MCTR2
CAS:<p>MCTR2, synthesized from DHA in macrophages, aids in tissue repair and reduces inflammation by promoting eicosanoid PGD2 and PGF2α decrease.</p>Fórmula:C27H40N2O6SCor e Forma:SolidPeso molecular:520.68FTI-2153 TFA
<p>FTI-2153 TFA inhibits farnesyltransferase with high selectivity (IC50: 1.4 nM), over 3000x more than Rap1A processing.</p>Fórmula:C27H31F3N4O5SCor e Forma:SolidPeso molecular:580.62Vicanicin
CAS:<p>Vicanicin is an aryl phenol ether compound found in lichens. It inhibits the expression of Hsp70, modulates intracellular redox-sensitive mechanisms, increases reactive oxygen species (ROS) in cancer cells, alters the Bax/Bcl-2 ratio, activates caspase-3, and induces apoptosis. Vicanicin suppresses cell growth and promotes apoptosis in androgen-sensitive (LNCaP) and androgen-insensitive (DU-145) human prostate cancer cells. It holds potential for prostate cancer research.</p>Fórmula:C18H16Cl2O5Cor e Forma:SolidPeso molecular:383.223DN-F01
<p>DN-F01 exhibits a potent calcium-dependent inhibitory effect on cardiac myofibrillar ATPase activity, with an IC50 of 11 ± 4 nmol/L.</p>Fórmula:C22H16N2O2Cor e Forma:SolidPeso molecular:340.37Tandutinib (MLN518) HCl
<p>Tandutinib antagonizes FLT3, PDGFR, and c-Kit with an IC50 of ~200 nM.</p>Fórmula:C31H43ClN6O4Pureza:98%Cor e Forma:SolidPeso molecular:599.16Monamycin H2
CAS:<p>Monamycin H2 is an ester peptide antibiotic that exhibits activity against Gram-positive bacteria.</p>Fórmula:C34H56ClN7O8Peso molecular:726.30De-N-methylpamamycin-593A
CAS:<p>De-N-methylpamamycin-593A is a 16-membered macrocyclic dilactone known for its ability to induce aerial mycelium formation.</p>Fórmula:C34H59NO7Peso molecular:593.84TT15
CAS:<p>TT15 is an agonist of the GLP-1R.</p>Fórmula:C51H44Cl2N4O6Cor e Forma:SolidPeso molecular:879.82Formadicin C
CAS:<p>Formadicin C exhibits the strongest activity among all components against certain strains of Pseudomonas, Proteus, and Alcaligenes.</p>Fórmula:C24H26N4O10Peso molecular:530.48Cuevaene A
CAS:<p>Cuevaene A can be isolated from the Streptomyces genus gdmAI-disrupted LZ35 strain. It exhibits moderate activity against Gram-positive bacteria, such as Bacillus subtilis (strain ATCC 11060), and demonstrates moderate activity against fungi, including Fusarium verticillioides (strain S68) and Rhizoctonia solani (strain GXE4).</p>Fórmula:C21H22O5Cor e Forma:SolidPeso molecular:354.396Griseorhodin G
CAS:<p>Griseorhodin G is a quinone antibiotic with antitumor activity.</p>Fórmula:C25H18O12Peso molecular:510.4020-HEDE
CAS:<p>20-HEDE (WIT 002) is a 20-hydroxyeicosatetraenoic acid (20-HETE) antagonist.</p>Fórmula:C20H36O3Pureza:98%Cor e Forma:SolidPeso molecular:324.50HS-731
CAS:<p>HS-731 is a μ-Opioid Receptor Agonist.</p>Fórmula:C20H26N2O5Cor e Forma:SolidPeso molecular:374.43SCP1-IN-1
CAS:<p>SCP1-IN-1 (SH T-62) is a potent inhibitor of SCP1, promoting REST degradation and potentially aiding glioblastoma research.</p>Fórmula:C20H19F3N2O7S2Pureza:99.53%Cor e Forma:SoildPeso molecular:520.5Maltophilin
CAS:<p>Maltophilin is a broad-spectrum antifungal antibiotic that exhibits no antibacterial activity against either Gram-positive or Gram-negative bacteria.</p>Fórmula:C29H38N2O6Peso molecular:510.62Polyoxin J
CAS:<p>Polyoxin J is a nucleoside antifungal antibiotic, notably effective against sheath blight in rice.</p>Fórmula:C17H25N5O12Peso molecular:491.41Antiplatelet agent 3
CAS:<p>Antiplatelet agent 3 (Compound K-10) is a compound with antiplatelet aggregation activity, exhibiting IC50 values of 2.55, 3.22, and 2.09 mg/mL for platelet aggregation induced by ADP, AA, and COL, respectively. It holds potential for research in cardiovascular diseases.</p>Fórmula:C38H32N2O5Cor e Forma:SolidPeso molecular:596.6715,6-Dihydro-4-methoxy-2H-pyran-2-one
CAS:<p>5,6-Dihydro-4-methoxy-2H-pyran-2-one is produced by the Penicillium italicum strain MRC 1360.</p>Fórmula:C6H8O3Peso molecular:128.13Monamycin G1
CAS:<p>Monamycin G1 is an ester-peptide antibiotic [esterpeptid]. It shows activity against Gram-positive bacteria.</p>Fórmula:C33H54ClN7O8Peso molecular:712.28Annonin VI
CAS:<p>Annonin VI is a natural inhibitor of NADH:ubiquinone oxidoreductase.</p>Fórmula:C37H66O7Cor e Forma:SolidPeso molecular:622.92Glaucarubin
CAS:<p>Glaucarubin is a bitter lactone naturally found in the fruits of Simaruba glauca. It is employed as an anti-amebic agent in research focused on amebiasis. The compound exhibits good tolerability, with a median lethal dose (LD50) of 1,600 mg/kg in mice and 6,400 mg/kg in rats.</p>Fórmula:C25H36O10Peso molecular:496.55Oryzoxymycin
CAS:<p>Oryzoxymycin is an aromatic derivative antibiotic with activity against Gram-negative bacteria.</p>Fórmula:C10H13NO5Peso molecular:227.21Dihydropergillin
CAS:<p>Dihydropergillin is produced by the Aspergillus terreus strain (ATCC 38849) and has the ability to inhibit plant growth.</p>Fórmula:C15H18O4Peso molecular:262.30Lucilactaene
CAS:<p>Lucilactaene exhibits potent antimalarial activity and functions as a P53-transfected tumor cell cycle inhibitor. It effectively halts the cell cycle progression of H1299/TSP53 cells at the G1 phase.</p>Fórmula:C22H27NO6Peso molecular:401.45MRS2279
CAS:<p>Selective, high affinity competitive antagonist of the P2Y1 receptor</p>Fórmula:C13H18ClN5O8P2Pureza:98%Cor e Forma:SolidPeso molecular:469.71Milbemycin α13
CAS:<p>Milbemycin α13 (Meilingmycin B) is an antibiotic that is effective against nematodes and mites.</p>Fórmula:C37H52O9Peso molecular:640.80Polyoxin K
CAS:<p>Polyoxin K is a nucleoside antifungal antibiotic that exhibits significant effectiveness against rice sheath blight.</p>Fórmula:C22H30N6O13Peso molecular:586.51JTE 151A
CAS:<p>JTE-151 is a novel RORγ inverse agonist.</p>Fórmula:C26H30ClN3O5Cor e Forma:SolidPeso molecular:499.99Papyracon D
CAS:<p>Papyracon D exhibits moderate inhibitory effects on L1210 and HL60 cells and shows mild inhibition against nematodes. It also has a slight inhibitory effect on Gram-positive bacteria.</p>Fórmula:C14H18O5Peso molecular:266.29PI3K-IN-23
<p>PI3K-IN-23 is a (E)-9-oxooctadec-10-en-12-ynoic acid analogue that promotes glucose uptake (EC50: 7.00 μM).</p>Fórmula:C24H33NO4SCor e Forma:SolidPeso molecular:431.59Melanoxazal
CAS:<p>Melanoxazal is an inhibitor of melanin biosynthesis, effectively suppressing melanin formation in silkworm larva hemolymph with an IC50 of 30.1 μg/mL, and it also exhibits strong inhibitory effects on mushroom tyrosinase (IC50 of 4.2 μg/mL), while lacking antibacterial activity.</p>Fórmula:C8H9NO3Peso molecular:167.16Hispidospermidin
CAS:<p>Hispidospermidin is a phospholipase C inhibitor.</p>Fórmula:C25H47N3OCor e Forma:SolidPeso molecular:405.66iMDK quarterhydrate
<p>iMDK quarterhydrate, PI3K inhibitor, blocks MDK growth; suppresses NSCLC safely with MEK inhibitor.</p>Fórmula:C21H15FN2O3SCor e Forma:SolidPeso molecular:380.91Norplicacetin
CAS:<p>Norplicacetin exhibits activity against Gram-positive bacteria and mycobacteria.</p>Fórmula:C24H33N5O7Peso molecular:503.55Amidinomycin
CAS:<p>Amidinomycin primarily acts against Gram-positive bacteria.</p>Fórmula:C9H18N4OPeso molecular:198.27Demycarosyl platenomycin
CAS:<p>Demycarosylplatenomycin (DM-PLM) is an antibiotic that exhibits mild activity against Gram-positive bacteria.</p>Fórmula:C31H51NO11Peso molecular:613.74Polyoxin L
CAS:<p>Polyoxin L is a nucleoside-type antifungal antibiotic that is notably effective against rice sheath blight.</p>Fórmula:C16H23N5O12Peso molecular:477.38Monamycin D1
CAS:<p>Monamycin D1 is a lipopeptide antibiotic with activity against Gram-positive bacteria.</p>Fórmula:C34H57N7O8Peso molecular:691.86Methylenomycin A
CAS:<p>Methylenomycin A is a cyclopentanone-derived antibiotic effective against both Gram-negative and Gram-positive bacteria.</p>Fórmula:C9H10O4Cor e Forma:SolidPeso molecular:182.173Danavorexton
CAS:<p>Danavorexton is an orexin receptor agonist.</p>Fórmula:C21H32N2O5SCor e Forma:SolidPeso molecular:424.55Azonafide-PEABA
CAS:<p>Azonafide-PEABA is a drug moiety with cytotoxic [1].</p>Fórmula:C32H33N5O4Pureza:98%Cor e Forma:SolidPeso molecular:551.64MB725
CAS:<p>MB725 is a strong and selective inducer of viability reduction in several cancer cell lines containing the oncogenic p53-Y220C mutation.</p>Fórmula:C18H21IN4O2SCor e Forma:SolidPeso molecular:484.35Glucosylceramide synthase-IN-3
<p>Glucosylceramide synthase-IN-3 (BZ1) is a potent, brain-accessible, oral GCS inhibitor with a 16 nM IC50, relevant for Gaucher's disease study.</p>Fórmula:C21H20FN3O3Cor e Forma:SolidPeso molecular:381.4Falecalcitriol
CAS:<p>Falecalcitriol is an analog of calcitriol. It has a higher potency both in vivo and in vitro systems, which is longer duration of action in vivo.</p>Fórmula:C27H38F6O3Pureza:98%Cor e Forma:SolidPeso molecular:524.58GLS1 Inhibitor-5
<p>GLS1 Inhibitor-5 (24y): Selective, oral glutaminase 1 inhibitor; IC50 68 nM; induces apoptosis; anti-tumor.</p>Cor e Forma:SolidNTPDase-IN-1
<p>NTPDase-IN-1 selectively inhibits NTPDases 1, 2, 8 with IC50 of 0.05, 0.23, 0.54 μM. Non-competitive, K m 21 μM, used in cancer, immune, infection research.</p>Fórmula:C18H25N3OS2Cor e Forma:SolidPeso molecular:363.54Z57346765
CAS:<p>Z57346765 is a specific PGK1 inhibitor that inhibits PGK1-dependent cell proliferation by decreasing the metabolic enzyme activity of PGK1 during glycolysis.</p>Fórmula:C17H18N4OPureza:99.85%Cor e Forma:SolidPeso molecular:294.35Napsagatran hydrate
CAS:<p>Napsagatran hydrate is a novel and specific inhibitor of thrombin.</p>Fórmula:C26H36N6O7SPureza:98%Cor e Forma:SolidPeso molecular:576.66Hazimycin 6
CAS:Hazimycin 6 exhibits weak activity against gram-negative bacteria, yeast, and dermatophytes.Fórmula:C20H18N4O4Cor e Forma:SolidPeso molecular:378.381Griseolutein A
CAS:<p>Griseolutein A exhibits activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C17H14N2O6Cor e Forma:SolidPeso molecular:342.303Herbicidin B
CAS:<p>Herbicidin B exhibits herbicidal properties and activity against Gram-positive bacteria.</p>Fórmula:C18H23N5O9Cor e Forma:SolidPeso molecular:453.4036-Hydroxytetrangulol
CAS:<p>6-Hydroxytetrangulol is an inducer of CPP32 protease found in Streptomyces.</p>Fórmula:C19H12O5Cor e Forma:SolidPeso molecular:320.30Pelagiomicin C
CAS:<p>Pelagiomicin C exhibits activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C17H15N3O5Cor e Forma:SolidPeso molecular:341.318Pentenocin A
CAS:<p>Pentenocin A exhibits a relatively weak inhibitory effect on IL-1 and β-glucuronidase (ICE) activity.</p>Fórmula:C7H10O5Cor e Forma:SolidPeso molecular:174.151Saframycin Mx2
CAS:<p>Saframycin Mx2 exhibits activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C29H38N4O8Cor e Forma:SolidPeso molecular:570.634GW311616 hydrochloride
CAS:<p>GW-311616 hydrochloride is a long duration, orally bioavailable, and selective human neutrophil elastase (HNE) inhibitor (IC50: 22 nM; Ki: 0.31 nM).</p>Fórmula:C19H32ClN3O4SPureza:98%Cor e Forma:SolidPeso molecular:433.99Epicillin
CAS:<p>Epicillin possesses antibacterial activity.</p>Fórmula:C16H21N3O4SCor e Forma:SolidPeso molecular:351.421Fleephilone
CAS:<p>Fleephilone is a fungal metabolite isolated from Trichoderma harzianum. It acts as an HIV REV/RRE binding inhibitor, hindering the interaction between REV protein and RRE RNA with an IC50 of 7.6 μM.</p>Fórmula:C24H27NO7Cor e Forma:SolidPeso molecular:441.474Harziphilone
CAS:<p>Harziphilone exhibits mild activity against Gram-positive bacteria and possesses antitumor properties, showing inhibitory effects on lymphocytic leukemia L1210 and leukemia P388 with an IC50 of 0.26 μg/mL. Additionally, Harziphilone inhibits the binding of the Rev protein to [33P]-labeled Rev response element (RRE) RNA, with an IC50 of 2.0 μM.</p>Fórmula:C15H18O4Cor e Forma:SolidPeso molecular:262.301Nemotin
CAS:<p>Nemotin exhibits activity against Gram-positive bacteria, mycobacteria, and fungi, while its effectiveness against Gram-negative bacteria is present but relatively weaker.</p>Fórmula:C11H8O2Cor e Forma:SolidPeso molecular:172.18Kahweol linoleate
CAS:<p>Kahweol linoleate, a semi-synthetic from coffee, blocks osteoclast creation, fights cancerous cells, prevents DNA damage, and reduces oxidative stress.</p>Fórmula:C38H56O4Cor e Forma:SolidPeso molecular:576.85Dihydrobisdechlorogeodin
CAS:<p>Dihydrobisdechlorogeodin, produced by the fungus strain [FO-4712] of the genus Acremonium, serves as a herbicide.</p>Fórmula:C17H16O7Cor e Forma:SolidPeso molecular:332.31ODN 2088
CAS:<p>ODN 2088 is a potent inhibitor of TLR3, TLR7 and TLR9 that is non-cytotoxic and shows inhibition of the release of IFN-α and IL-6.</p>Cor e Forma:SolidHypercalin B
CAS:<p>Hypercalin B is an antibacterial agent isolated from the hexane and chloroform extracts of Hypericum acmosepalum. It demonstrates activity against multidrug-resistant strains of Staphylococcus aureus, with a minimum inhibitory concentration (MIC) ranging from 0.5 to 128 mg/L.</p>Fórmula:C33H42O5Cor e Forma:SolidPeso molecular:518.6843,4-Dimethoxytropolone
CAS:<p>3,4-Dimethoxytropolone can be isolated from the fermentation broth of Streptoverticillium hadanonense, and it shows activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C9H10O4Cor e Forma:SolidPeso molecular:182.173Imolamine hydrochloride
CAS:<p>Imolamine hydrochloride is a blood platelet aggregation antagonist.</p>Fórmula:C14H21ClN4OCor e Forma:SolidPeso molecular:296.80Oiligodendrocyte differentiation promoter 1
CAS:<p>Oiligodendrocyte differentiation promoter 1 is a promoter of oiligodendrocyte differentiation .</p>Fórmula:C25H25Cl2NO5Pureza:98%Cor e Forma:SolidPeso molecular:490.38Difeterol
CAS:<p>Difeterol is a biochemical.</p>Fórmula:C25H29NO2Cor e Forma:SolidPeso molecular:375.50SPR7
<p>SPR7 is a potent and selective rhodesain inhibitor (Ki: 0.51 nM). SPR7 exhibited antiparasitic effects against T. b. brucei (EC50: 1.65 μM).</p>Fórmula:C30H32ClN3O3Cor e Forma:SolidPeso molecular:518.05Luffolide
CAS:<p>Luffolide, a Luffariella sponge metabolite, shares manoalide's anti-inflammatory traits and fully inhibits PLA2's cleavage of phosphatidylcholine.</p>Fórmula:C27H40O6Cor e Forma:SolidPeso molecular:460.6023-De(mycinosyloxy)tylosin
CAS:<p>23-De(mycinosyloxy)tylosin is a macrolide antibiotic exhibiting activity against Gram-positive bacteria, with limited efficacy against Gram-negative bacteria and mycoplasma.</p>Fórmula:C38H63NO12Cor e Forma:SolidPeso molecular:725.91GC 14
CAS:<p>GC 14 is a selective thyroid hormone receptor antagonist, with IC50 values of 200 nM and 35 nM for hTRα and hTRβ, respectively.</p>Fórmula:C26H27NO6Pureza:98%Cor e Forma:SolidPeso molecular:449.5ONO-AE1-259 lysine
CAS:<p>ONO-AE1-259 is a highly selective agonist of prostaglandin e2 receptor (ep2)</p>Fórmula:C28H49ClN2O6Cor e Forma:SolidPeso molecular:545.15Mycinamicin Ⅵ
CAS:<p>Mycinamicin VI is a macrolide antibiotic with antibacterial activity against Gram-positive bacteria.</p>Fórmula:C35H57NO11Cor e Forma:SolidPeso molecular:667.83Megovalicin G
CAS:<p>Megovalicin G is effective against Bacillus subtilis and Escherichia coli, and it also acts on Pseudomonas aeruginosa.</p>Fórmula:C35H61NO7Cor e Forma:SolidPeso molecular:607.86Monamycin B
CAS:<p>Monamycin B is an ester peptide antibiotic with activity against Gram-positive bacteria.</p>Fórmula:C33H55N7O8Cor e Forma:SolidPeso molecular:677.83FR-900482
CAS:<p>FR-900482 exhibits high sensitivity to Thermoactinomyces calidolactis strain C 953 and demonstrates activity against cell lines such as P388, B16, EL4, FM3A, L1210, BHK-21, among others.</p>Fórmula:C14H15N3O6Cor e Forma:SolidPeso molecular:321.299-Hydroxycrisamicin
CAS:<p>9-Hydroxycrisamicin exhibits moderate activity against Gram-positive bacteria with a minimum inhibitory concentration (MIC) ranging from 6.25 to 25 μg/mL. Additionally, 9-Hydroxycrisamicin demonstrates significant growth inhibition towards various human tumor cell lines.</p>Fórmula:C32H22O13Cor e Forma:SolidPeso molecular:614.51Dictyopanine A
CAS:<p>Dictyopanine A exhibits a relatively narrow antibacterial spectrum, demonstrating moderate antimicrobial activity only against certain filamentous fungi and Gram-positive bacteria.</p>Fórmula:C25H34O5Cor e Forma:SolidPeso molecular:414.53Monamycin I
CAS:<p>Monamycin I is an ester peptide antibiotic with activity against Gram-positive bacteria.</p>Fórmula:C35H58ClN7O8Cor e Forma:SolidPeso molecular:740.33RIP1 kinase inhibitor 1
CAS:<p>RIP1 kinase inhibitor 1 is an orally available and brain-penetrating inhibitor of RIP1 kinase with pKi of 9.04.</p>Fórmula:C24H20ClN5O3Pureza:98%Cor e Forma:SolidPeso molecular:461.9Chitinase-IN-4
<p>Chitinase-IN-4 (compound 8f) is a potent and selective inhibitor of OfChi-h with an IC50 value of 0.1 μM and good insecticidal activity.</p>Fórmula:C21H24ClN7Cor e Forma:SolidPeso molecular:409.925-Deoxygentamicin C1
CAS:<p>5-Deoxygentamicin C1 exhibits activity against both gram-positive and gram-negative bacteria.</p>Fórmula:C21H43N5O6Cor e Forma:SolidPeso molecular:461.60TAM&Met-IN-1
CAS:<p>TAM&Met-IN-1 inhibits AXL, MER, TYRO3 with IC50s 6.1, 13.2, 21.6 nM, respectively, for cancer research.</p>Fórmula:C29H27F2N7O5Cor e Forma:SolidPeso molecular:591.57Anticancer agent 26
<p>Anticancer agent 26 is a promising candidate for cancer therapy and deserves further development.</p>Fórmula:C28H33NO5Cor e Forma:SolidPeso molecular:463.57DWN-12088 HCl
CAS:<p>DWN-12088 HCl is the salt form of DWN-12088 Free Base, an orally administered small molecule prolyl-tRNA synthetase (PRS) inhibitor</p>Fórmula:C15H21Cl4N3OCor e Forma:SolidPeso molecular:401.15Mepixetil
<p>Mepixetil is a potent angiotensin II receptor antagonist[1].</p>Fórmula:C12H18N2O3Cor e Forma:SolidPeso molecular:238.28ErSO-DFP
<p>ErSO-DFP activates a-UPR, targets ERα+ cancer cells with high selectivity, and effectively reduces MCF-7 tumours.</p>Fórmula:C20H17F5N2O2Cor e Forma:SolidPeso molecular:412.35Pefcalcitol
CAS:<p>Pefcalcitol is a novel antipsoriatic prodrug candidate containing a 16-en-22-oxa-vitamin D3 structure.</p>Fórmula:C26H34F5NO4Cor e Forma:SolidPeso molecular:519.54Rimegepant sulfate hydrate
CAS:<p>Rimegepant (BMS-927711/BHV-3000): oral CGRP blocker for migraines, effective without vasoconstriction, beats placebo, well-tolerated.</p>Fórmula:C56H64F4N12O13SCor e Forma:SolidPeso molecular:1221.2526Retezorogant
CAS:<p>Retezorogant is a retinoic acid receptor-related orphan receptor gamma (RORγ) antagonist.</p>Fórmula:C23H33ClN2O3Cor e Forma:SolidPeso molecular:420.97Pyrisulfoxin B
CAS:<p>Pyrisulfoxin B is an antibiotic produced by the bacterium Streptomyces (BS-75).</p>Fórmula:C13H11N3O2SCor e Forma:SolidPeso molecular:273.31AZ0108
CAS:<p>AZ0108, an oral PARP1,2,6 inhibitor, selectively blocks centrosome clustering, is viable for in vivo studies, and doesn't inhibit PARP3/TNKS1.</p>Fórmula:C24H20F4N6O2Cor e Forma:SolidPeso molecular:500.45AVE 0991
CAS:<p>AVE 0991 is a nonpeptide analog of angiotensin-(1-7), a Mas agonist with inhibitory effects on [125I]-Ang-(1-7) and on neuroinflammation in Alzheimer's disease.</p>Fórmula:C29H32N4O5S2Pureza:98.69%Cor e Forma:SolidPeso molecular:580.72Enpp-1-IN-12
<p>ENPP1-IN-12 is a potent, oral ENPP1 inhibitor with a Ki of 41 nM and anti-tumor properties.</p>Fórmula:C17H19N5O3SCor e Forma:SolidPeso molecular:373.43Keap1-Nrf2-IN-1 TFA
<p>Keap1-Nrf2-IN-1 TFA (compound35) is a potent inhibitor (IC50: 43 nM) protecting against acetaminophen liver damage.</p>Fórmula:C26H25F3N2O9SCor e Forma:SolidPeso molecular:598.54P2X receptor-1
<p>P2X receptor-1 is a potential inhibitor of P2X receptor for the treatment of pain and inflammation.</p>Fórmula:C14H14ClN3O3S2Cor e Forma:SolidPeso molecular:371.86ZK824859 hydrochloride (2271122-53-1 free base)
<p>ZK824859 hydrochloride: oral, selective uPA inhibitor, IC50s: 79 nM (uPA), 1580 nM (tPA), 1330 nM (plasmin).</p>Fórmula:C23H23ClF2N2O4Pureza:98%Cor e Forma:SolidPeso molecular:464.89PCSK9-IN-16
CAS:<p>PCSK9-IN-16, holds potential for research into hypercholesterolemia and other cardiovascular diseases [1].</p>Fórmula:C16H20N6O2S3Cor e Forma:SolidPeso molecular:424.56Aplysin
CAS:<p>Aplysin suppresses breast cancer cells and protects liver cells by blocking PI3K/AKT/FOXO3a and preventing oxidative damage.</p>Fórmula:C15H19BrOCor e Forma:SolidPeso molecular:295.21Zetomipzomib
CAS:<p>KZR-616: Immunoproteasome inhibitor targeting LMP7 (IC50: 39/57 nM) & LMP2 (IC50: 131/179 nM), potential in autoimmune disease research.</p>Fórmula:C30H42N4O8Cor e Forma:SolidPeso molecular:586.6820-Deoxynarasin
CAS:<p>20-Deoxynarasin exhibits activity against Gram-positive bacteria, mycoplasma, coccidia, and viruses, and it also promotes growth.</p>Fórmula:C43H72O10Cor e Forma:SolidPeso molecular:749.03SPR-00305
CAS:<p>SPR-00305 is a novel potent inhibitor of the mvfr pathway</p>Fórmula:C24H19ClN2O3Cor e Forma:SolidPeso molecular:418.87GSK1820795A
CAS:<p>GSK1820795A: Telmisartan analog, selective hGPR132a antagonist, blocks yeast activation by N-acylamides, angiotensin II antagonist, partial PPARγ agonist.</p>Fórmula:C35H34N8Cor e Forma:SolidPeso molecular:566.7Domitroban
CAS:<p>Domitroban, also known as S-145, is a thromboxane (Tx) A2-receptor antagonist with partial agonistic activity in vascular smooth muscle.</p>Fórmula:C20H27NO4SCor e Forma:SolidPeso molecular:377.5Kigamicin B
CAS:<p>Kigamicin B exhibits activity against gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA), with a minimum inhibitory concentration (MIC) ranging from 0.025 to 0.78 μg/mL.</p>Fórmula:C40H45NO15Cor e Forma:SolidPeso molecular:779.78Phenazostatin B
CAS:<p>Phenazostatin B is a phenazine derivative known for its neuroprotective properties. It acts by scavenging free radicals, protecting N18-RE 105 neuronal cells from glutamate-induced toxicity, and inhibiting lipid peroxidation. It inhibits glutamate toxicity in N18-RE-105 cells, with an EC50 of 0.33 μg/mL.</p>Fórmula:C32H26N4O4Cor e Forma:SolidPeso molecular:530.57PEN-866
CAS:<p>PEN-866, a conjugate of HSP90i and SN-38, may control early NSCLC tumor growth.</p>Fórmula:C49H49N7O9Cor e Forma:SolidPeso molecular:879.95Oberadilol
CAS:<p>Oberadilol is a pyridazinone derivative with vasodilatory and beta-adrenergic blocking activities and type III phosphodiesterase inhibitory action</p>Fórmula:C25H30ClN5O3Cor e Forma:SolidPeso molecular:483.99hTrkA-IN-2
<p>hTrkA-IN-2 is a selective hTrkA metamorphosis inhibitor (IC50: 3.9 nM).</p>Fórmula:C24H22F3N5O3Cor e Forma:SolidPeso molecular:485.46THR-β agonist 4
CAS:<p>THR-β agonist 4 is a potent agonist of THR-β.</p>Fórmula:C16H11Cl2F2N5O6SCor e Forma:SolidPeso molecular:510.26Oral antiplatelet agent 1
CAS:<p>Oral antiplatelet agent 1 is a potent antiplatelet agent with an IC50 of 2.94 μM in vitro.</p>Fórmula:C23H24N4O5SPureza:98%Cor e Forma:SolidPeso molecular:468.53Cinnatriacetin A
CAS:<p>Cinnatriacetin A exhibits activity against Gram-positive bacteria.</p>Fórmula:C23H20O5Cor e Forma:SolidPeso molecular:376.402Coriolin A
CAS:<p>Coriolin A exhibits activity against gram-positive bacteria, weakly against gram-negative bacteria, as well as yeasts and Trichomonas vaginalis. At a concentration of 5 μg/mL, it inhibits 61.6% of the growth of Yoshida sarcoma, but shows no inhibitory effect on Ehrlich ascites carcinoma in animals.</p>Fórmula:C15H20O5Cor e Forma:SolidPeso molecular:280.316Lipohexin
CAS:<p>Lipohexin is a peptide antibiotic that exhibits activity against Gram-positive bacteria. It competitively inhibits human placental proline endopeptidase (proline endopeptidase) with an IC50 of 3.5 μM. Additionally, Lipohexin inhibits proline endopeptidase from Flavobacterium meningosepticum, with an IC50 of 25 μM.</p>Fórmula:C39H68N6O9Cor e Forma:SolidPeso molecular:764.992Leucomycin A6
CAS:<p>Leucomycin A6 effectively combats Gram-positive bacteria.</p>Fórmula:C41H67NO14Cor e Forma:SolidPeso molecular:797.969CB-7646
CAS:<p>CB-7646 is a stable trimelamol (TM) analogue, which is an antitumor agent.</p>Fórmula:C8H16N6O2Cor e Forma:SolidPeso molecular:228.25Coriolin B
CAS:<p>Coriolin B exhibits activity against Gram-positive bacteria, weak activity against Gram-negative bacteria, yeast, and Trichomonas vaginalis. At a concentration of 5 μg/mL, Coriolin B inhibits 61.6% of Yoshida sarcoma growth but shows no inhibitory effect on Ehrlich ascites carcinoma in animals.</p>Fórmula:C23H36O6Cor e Forma:SolidPeso molecular:408.528Salfredin C3
CAS:<p>Salfredin C3 is an inhibitor of aldose reductase (aldose reductase).</p>Fórmula:C16H15NO8Cor e Forma:SolidPeso molecular:349.292Griseolic acid C
CAS:<p>Griseolic acid C (Dihydrodeoxygriseolic acid) is an antibiotic found in the Streptomyces griseoaurantiacus SANK43894 strain. This compound is a potent inhibitor of cyclic adenosine monophosphate (cAMP) phosphodiesterase [EC 3.1.4.17], with an IC50 of 0.12 μM (enzyme sourced from rat brain tissue).</p>Fórmula:C14H15N5O7Cor e Forma:SolidPeso molecular:365.298Hcyb1
<p>Hcyb1 specifically inhibits PDE2A with 0.57 μM IC50, over 250x selective, and has neuroprotective and antidepressant effects.</p>Fórmula:C24H20N4OCor e Forma:SolidPeso molecular:380.44MU1656
CAS:<p>MU1656 is a selective inhibitor of histone methyltransferase DOT1L, which significantly inhibits cancer cell proliferation in hematological malignancies.</p>Fórmula:C32H45N7O2Pureza:96.92%Cor e Forma:SolidPeso molecular:559.75Rhodomycin B
CAS:<p>Rhodomycin B exhibits activity against Gram-positive bacteria, while its effects on Gram-negative bacteria and fungi are relatively weak.</p>Fórmula:C28H33NO10Cor e Forma:SolidPeso molecular:543.562Saframycin B
CAS:<p>Saframycin B exhibits activity against Gram-positive bacteria and has weaker efficacy against mycobacteria.</p>Fórmula:C28H31N3O8Cor e Forma:SolidPeso molecular:537.561Azicemicin A
CAS:<p>Azicemicin A exhibits mild antibacterial activity and shows no acute toxicity when administered via intraperitoneal injection to mice at a dosage of 150 mg/kg.</p>Fórmula:C23H25NO9Cor e Forma:SolidPeso molecular:459.446Kynapcin-28
CAS:<p>Kynapcin-28 is a non-competitive inhibitor of prolyl endopeptidase (PEP) with an IC50 of 76.80 μM and exhibits weak inhibitory effects on other serine proteases.</p>Fórmula:C19H12O10Cor e Forma:SolidPeso molecular:400.293Deoxyradicinin
CAS:<p>Deoxyradicinin is a biosynthetic precursor of Radicinin. It can inhibit Xylella fastidiosa and Liberibacter crescens, with a minimum inhibitory concentration (MIC) of 3.5 μg/mL against Liberibacter crescens. Deoxyradicinin is applicable for research on controlling plant diseases caused by these pathogens.</p>Fórmula:C12H12O4Cor e Forma:SolidPeso molecular:220.221Cremeomycin
CAS:<p>Cremeomycin exhibits activity against Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA), with a minimum inhibitory concentration (MIC) of 0.2-0.39 μg/mL. It also demonstrates cytotoxic effects in vitro against mouse tumor cell lines P388, L1210, IMC, S180, B16, and SS3.</p>Fórmula:C8H6N2O4Cor e Forma:SolidPeso molecular:194.144Polyozellin
CAS:<p>Polyozellin is a prolyl endopeptidase inhibitor with properties effective against inflammation, cancer, and diseases related to oxidative stress.</p>Fórmula:C22H14O10Cor e Forma:SolidPeso molecular:438.341Salfredin C1
CAS:<p>Salfredin C1 is an inhibitor of aldose reductase.</p>Fórmula:C13H11NO6Cor e Forma:SolidPeso molecular:277.229Phencomycin
CAS:<p>Phencomycin exhibits mild activity against Gram-positive bacteria and inhibits physiologically important enzymes such as renin, with an IC50 of 440 μg/mL.</p>Fórmula:C15H10N2O4Cor e Forma:SolidPeso molecular:282.251Diatretyne Ⅰ
CAS:Diatretyne I (Diatretyne amide) exhibits mild activity against Gram-positive bacteria.Fórmula:C8H5NO3Cor e Forma:SolidPeso molecular:163.13XR8-89
CAS:<p>XR8-89, a potent PLpro inhibitor (IC50=0.1μM), blocks SARS-CoV-2 replication; useful for research.</p>Fórmula:C29H36N4O2SCor e Forma:SolidPeso molecular:504.69Crotocin
CAS:<p>Crotocin exhibits bactericidal activity against Cryptococcus neoformans, Candida albicans, and Saccharomyces cerevisiae (brewer’s yeast), but it can be inactivated by blood.</p>Fórmula:C19H24O5Cor e Forma:SolidPeso molecular:332.391SAR107375
CAS:<p>SAR107375 is a potent, orally active dual inhibitor of thrombin and factor Xa, with K_i values of 1 nM and 8 nM for factor Xa and thrombin, respectively [1].</p>Fórmula:C24H30ClN5O5S2Cor e Forma:SolidPeso molecular:568.11Enactin Ia
CAS:<p>Enactin Ia is found in Streptomyces roseoviridis and exhibits mild antibacterial activity.</p>Fórmula:C20H38N2O6Cor e Forma:SolidPeso molecular:402.526Kurasoin A
CAS:<p>Kurasoin A is an inhibitor of the enzyme farnesyltransferase.</p>Fórmula:C16H16O3Cor e Forma:SolidPeso molecular:256.296Piloquinone
CAS:<p>Piloquinone is a type of phenanthrene compound that exhibits mild inhibitory effects on mycobacteria and protozoa.</p>Fórmula:C21H20O5Cor e Forma:SolidPeso molecular:352.38Azirinomycin
CAS:<p>Azirinomycin exhibits activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C4H5NO2Cor e Forma:SolidPeso molecular:99.088ZK159222
CAS:<p>ZK159222 is an effective 1α,25-(OH)2D3 receptor (VDR) agonist. ZK159222 has a partial agonistic character.</p>Fórmula:C32H48O5Pureza:98%Cor e Forma:SolidPeso molecular:512.721-Deamino-1-hydroxysagamicin
CAS:<p>1-Deamino-1-hydroxysagamicin (AntibioticSUM-3) is an aminoglycoside antibiotic that is effective against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C20H40N4O8Cor e Forma:SolidPeso molecular:464.554Symplostatin 1
CAS:<p>Symplostatin 1 is a dolastatin 10 analog from the marine cyanobacterium Symploca hydnoides.</p>Fórmula:C43H70N6O6SCor e Forma:SolidPeso molecular:799.12GNE-616
CAS:<p>GNE-616: a potent, stable, oral Nav1.7 inhibitor; Ki: 0.79 nM, Kd: 0.38 nM; for chronic pain.</p>Fórmula:C24H23F4N5O3SPureza:98%Cor e Forma:SolidPeso molecular:537.53Pyrrolomycin A
CAS:<p>Pyrrolomycin A is a pyrrole antibiotic that exhibits activity against Gram-positive bacteria, Gram-negative bacteria, and fungi.</p>Fórmula:C4H2Cl2N2O2Cor e Forma:SolidPeso molecular:180.977NSC 357754
CAS:<p>NSC 357754 is an inhibitor of Claudin. It can enhance transepithelial electrical resistance and reduce specific cation permeability. NSC 357754 is useful for research involving Claudin-2 and/or Claudin-15 mediated intestinal disorders.</p>Fórmula:C26H20N4O2Cor e Forma:SolidPeso molecular:420.463DMP-728 free base
CAS:<p>DMP-728 free base is a highly potent and selective GPIIbDIIa antagonist</p>Fórmula:C25H36N8O7Cor e Forma:SolidPeso molecular:560.60O-Desmethyl Midostaurin
CAS:<p>O-Desmethyl Midostaurin is the active Midostaurin metabolite via cytochrome P450 liver enzyme metabolism.</p>Fórmula:C34H28N4O4Pureza:98%Cor e Forma:SolidPeso molecular:556.61Miyakamide A2
CAS:<p>Miyakamide A2 is an antibiotic with insecticidal properties. It inhibits the growth of brine shrimp and exhibits weak activity against Xanthomonas species. The IC50 for inhibiting P388 cells is 12.2 μg/mL.</p>Fórmula:C31H32N4O3Cor e Forma:SolidPeso molecular:508.611Fluoropolyoxin L
CAS:<p>Fluoropolyoxin L exhibits inhibitory activity against Escherichia coli and Enterococcus faecalis.</p>Fórmula:C16H22FN5O12Cor e Forma:SolidPeso molecular:495.371NTPDase-IN-2
CAS:<p>NTPDase-IN-2 inhibits h-NTPDase-2/-8 (IC50: 0.04, 2.27 µM), non-competitive for h-NTPDase-1/-2 (Km: 74 µM); useful in cancer, immune, bacterial research.</p>Fórmula:C24H20FN3OS2Cor e Forma:SolidPeso molecular:449.56Dephostatin
CAS:<p>Dephostatin is a competitive protein tyrosine phosphatase (PTP) inhibitor isolated from Streptomyces spp., exhibiting activity within the micromolar range.</p>Fórmula:C7H8N2O3Cor e Forma:SolidPeso molecular:168.153HKT-IN-1
CAS:<p>3HKT-IN-1 (Compound 17122279) is an inhibitor of Anopheles gambiae 3-hydroxykynurenine transaminase (3HKT) and is utilized in malaria research.</p>Fórmula:C12H11BrN2O3Cor e Forma:SolidPeso molecular:311.131Peptaibolin
CAS:<p>Peptaibolin exhibits activity against Gram-positive bacteria and yeast. The minimum inhibitory concentration (MIC) for its effect on Bacillus subtilis [ATCC 6633] and Candida albicans is 100 μg/mL.</p>Fórmula:C31H51N5O6Cor e Forma:SolidPeso molecular:589.77Tzc 5665
CAS:<p>Tzc 5665 is a pyridazinone derivative with vasodilatory and beta-adrenergic blocking activities and type III phosphodiesterase inhibitory action.</p>Fórmula:C31H38ClN5O7Cor e Forma:SolidPeso molecular:628.12PCTR1
CAS:<p>PCTR1, derived from DHA, hastens inflammation resolution and boosts macrophage function, reducing PGE2, PGD2, and TXB2 in mice.</p>Fórmula:C32H47N3O9SCor e Forma:SolidPeso molecular:649.8Megovalicin A
CAS:<p>Megovalicin A is effective against Bacillus subtilis and Escherichia coli.</p>Fórmula:C35H63NO8Cor e Forma:SolidPeso molecular:625.8820-Deoxysalinomycin
CAS:<p>20-Deoxysalinomycin primarily targets Gram-positive bacteria, with a particular effectiveness against poultry coccidia.</p>Fórmula:C42H70O10Cor e Forma:SolidPeso molecular:735.00VU6028418
<p>VU6028418 is a highly selective, potent, orally active M4mAChR antagonist that acts on hM4 (IC50: 4.1 nM).</p>Cor e Forma:LiquidPradimicin B
CAS:<p>Pradimicin B is an antibiotic with potent antifungal and anti-yeast activities.</p>Fórmula:C35H36N2O14Cor e Forma:SolidPeso molecular:708.665Calphostin D
CAS:<p>Calphostins, PKC inhibitors from Cladosporium cladosporioides, include A, B, C, D, I; C is most potent.</p>Fórmula:C30H30O10Cor e Forma:SolidPeso molecular:550.55BSc5367
CAS:<p>BSc5367 inhibits Nek1 kinase (IC50: 11.5 nM), key in cell cycle, DNA repair, impacting ALS, PKD, cancer.</p>Fórmula:C20H15N3O2Cor e Forma:SoildPeso molecular:329.35Exfoliazone
CAS:<p>Exfoliazone is a phenazinic antibiotic with activity against Trichoderma viride, exhibiting an ED50 for inhibiting mycelial growth of 70 μg/mL.</p>Fórmula:C15H12N2O4Cor e Forma:SolidPeso molecular:284.267Dynemicin Q
CAS:<p>Dynemicin Q is an antibiotic that demonstrates potent activity against Gram-positive bacteria.</p>Fórmula:C28H19NO9Cor e Forma:SolidPeso molecular:513.45Hydrolyzed Fumonisin B2
CAS:<p>Hydrolyzed Fumonisin B2 (HFB2) is a hydrolysis product of fumonisins (HF), which retains biological activity. It exhibits phytotoxicity.</p>Fórmula:C22H47NO4Pureza:98%Cor e Forma:SolidPeso molecular:389.61AN-12-H5
CAS:<p>AN-12-H5 is an anti-enteroviral compound that targets the replication process of PV and EV71 viruses.</p>Fórmula:C24H23N3O4S3Cor e Forma:SolidPeso molecular:513.65Sulprostone
CAS:<p>EP3 and EP1 receptor agonist</p>Fórmula:C23H31NO7SPureza:98%Cor e Forma:White To Off-White SolidPeso molecular:465.56Prohibitin ligand 1
<p>Compound 22i, a prohibitin ligand, protects the heart at nanomolar levels by inducing STAT3 phosphorylation.</p>Fórmula:C20H22N2OCor e Forma:SolidPeso molecular:306.4Pyridoxatin
CAS:<p>Pyridoxatin: fungal metabolite; blocks TBARS production, prevents AAPH-induced hemolysis, and acts against C. albicans.</p>Fórmula:C15H21NO3Cor e Forma:SolidPeso molecular:263.33Celesticetin B
CAS:<p>Celesticetin B is an antibiotic primarily exhibiting antibacterial activity against Gram-positive microorganisms.</p>Fórmula:C21H38N2O8SCor e Forma:SolidPeso molecular:478.6(1R,3S)-THCCA-Asn
<p>(1R,3S)-THCCA-Asn (4j) is a selective inhibitor of thrombin (IC50: 0.07-0.14 μM) with anti-thrombotic effects.</p>Fórmula:C24H24N4O6Cor e Forma:SolidPeso molecular:464.47Leucomycin U
CAS:<p>Leucomycin U is a macrolide antibiotic. It demonstrates significant activity against Gram-positive bacteria and also exhibits effects on spirochetes, rickettsiae, and chlamydiae.</p>Fórmula:C37H61NO14Cor e Forma:SolidPeso molecular:743.878Gilvusmycin
CAS:<p>Gilvusmycin is an antibiotic with potent antitumor properties. It effectively inhibits the proliferation of P388, K562, A431, and MKN28 cells, with IC50 values (ng/mL) of 0.08, 0.86, 0.72, and 0.75, respectively.</p>Fórmula:C38H34N6O8Cor e Forma:SolidPeso molecular:702.712Unoprostone
CAS:<p>Unoprostone is a prostaglandin F2α analogs (PGAs), and reduces intraocular pressure and is used topically for glaucoma or ocular hypertension.</p>Fórmula:C22H38O5Pureza:98%Cor e Forma:SolidPeso molecular:382.53Atiratecan
CAS:<p>Atiratecan (TP300), a CH0793076-based camptothecin prodrug, combats BCRP+/- tumors; doesn't affect AChE.</p>Fórmula:C31H34N6O6Pureza:98%Cor e Forma:SolidPeso molecular:586.64Thielavin B
CAS:<p>Thielavin B, from Thielavia terricola, inhibits prostaglandin E2 synthesis and reduces rat oedema.</p>Fórmula:C31H34O10Cor e Forma:SolidPeso molecular:566.6PRN694
CAS:<p>PRN694 is a potent, irreversible ITK/RLK inhibitor with IC50s: 0.3/1.4 nM; offers lasting effector cell suppression.</p>Fórmula:C28H35F2N5O2SPureza:98%Cor e Forma:SolidPeso molecular:543.67SSTR5 antagonist 2 TFA
CAS:<p>Potent, oral SSTR5 antagonist 2 TFA may treat type 2 diabetes.</p>Fórmula:C34H36F4N2O7Pureza:98%Cor e Forma:SolidPeso molecular:660.65MK-8970
<p>MK-8970 is an acetal carbonate prodrug of raltegravir with enhanced colonic absorption.</p>Fórmula:C25H29FN6O8Cor e Forma:SolidPeso molecular:560.542-Hydroxy-5-iminoazacyclopent-3-ene
CAS:<p>2-Hydroxy-5-iminoazacyclopent-3-ene is a pyrroline-class antibiotic with mild activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C4H6N2OCor e Forma:SolidPeso molecular:98.103AMPK Activator SC4
CAS:<p>SC4 is a potent, direct AMPK activator. SC4 preferentially activates α2 complexes and stimulates skeletal muscle glucose uptake.</p>Fórmula:C26H18ClN3O4Cor e Forma:SolidPeso molecular:471.89
