Otros inhibidores
Esta categoría abarca una amplia variedad de inhibidores que no encajan en las clasificaciones estándar, pero que son fundamentales para diversas investigaciones bioquímicas y farmacológicas. Estos inhibidores pueden dirigirse a vías, enzimas e interacciones moleculares únicas o menos estudiadas, proporcionando herramientas valiosas para áreas de investigación especializadas. En CymitQuimica, ofrecemos una selección diversa de inhibidores de alta calidad que abarcan múltiples objetivos biológicos y disciplinas de investigación, lo que le permite explorar nuevas vías terapéuticas y profundizar su comprensión de los procesos biológicos complejos.
Se han encontrado 37902 productos de "Otros inhibidores"
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Chelocardin
CAS:<p>Chelocardin exhibits activity against Gram-positive and Gram-negative bacteria.</p>Fórmula:C22H21NO7Forma y color:SolidPeso molecular:411.405Carbacyclin
CAS:<p>Carbacyclin, a PGI2 analog, is a prostacyclin (PGI2) receptor agonist and vasodilator with potent inhibitory platelet aggregation.</p>Fórmula:C21H34O4Pureza:98%Forma y color:SolidPeso molecular:350.49HR-546
CAS:<p>HR-546 is a prostaglandin E2 and prostaglandin F2alpha antagonist.</p>Fórmula:C26H44O6Forma y color:SolidPeso molecular:452.62Heme Oxygenase-1-IN-3
CAS:<p>Heme Oxygenase-1-IN-3 (compound 4) serves as a potent and selective inhibitor of heme oxygenase-1 (HO-1) with a dissociation constant (Kd) of 141 nM, making it suitable for use in cancer and neurodegenerative disease research.</p>Fórmula:C22H18BrFN4O2SForma y color:SolidPeso molecular:501.37CEP-2563
CAS:<p>CEP-2563 is a prodrug of CEP-751. It also used as an antitumor agent, inhibiting protein kinases.</p>Fórmula:C36H41ClN6O6Pureza:98%Forma y color:SolidPeso molecular:689.20Dehydelone
CAS:<p>Dehydelone(KOS-1584, R-1645, SK-10088) is a microtubule stabilizer that may be used in the treatment of non-small cell lung cancer.</p>Fórmula:C27H39NO5SForma y color:SolidPeso molecular:489.674-Chloropyridine
CAS:<p>4-Chloropyridine acts as an inhibitor of Nicotinamide N-methyltransferase (NNMT). Serving as a substrate for NNMT, this compound enhances the electrophilicity at the C4 position through methylation of the pyridine nitrogen. This modification facilitates an aromatic nucleophilic substitution reaction with the non-catalytic cysteine (C159) in NNMT, ultimately leading to suicidal activity inhibition of the enzyme. 4-Chloropyridine is a promising candidate for the development of activity-based probes targeting NNMT functions.</p>Fórmula:C5H4ClNForma y color:SolidPeso molecular:113.55PF-06305591 dihydrate
<p>PF-06305591 dihydrate is a potent and highly selective voltage gated sodium channel NaV1.8 blocker (IC 50 = 15 nM) with an excellent preclinical in vitro ADME</p>Fórmula:C15H26N4O3Forma y color:SolidPeso molecular:310.39JTE 151A
CAS:<p>JTE-151 is a novel RORγ inverse agonist.</p>Fórmula:C26H30ClN3O5Forma y color:SolidPeso molecular:499.99LI-3948
CAS:<p>IP6K-IN-2 (compound 29c) is an IP6K inhibitor that demonstrates oral bioavailability and the ability to permeate the blood-brain barrier (IC 50 : 15.8 nM), making it suitable for research on central nervous system diseases.</p>Fórmula:C19H16Cl2FN3O3Forma y color:SolidPeso molecular:424.25Cinatrin A
CAS:<p>Cinatrin A exhibits inhibitory activity against phospholipase A2 (phospholipaseA2).</p>Fórmula:C18H26O8Forma y color:SolidPeso molecular:370.394GW311616
CAS:<p>GW-311616 is a long duration, orally bioavailable, and selective human neutrophil elastase (HNE) inhibitor (IC50: 22 nM; Ki: 0.31 nM).</p>Fórmula:C19H31N3O4SForma y color:SolidPeso molecular:397.53L-739750
CAS:<p>L-739,750 is an inhibitor (FTI) of peptidomimetic farnesyltransferase.</p>Fórmula:C23H39N3O6S2Pureza:98%Forma y color:SolidPeso molecular:517.7Cenicriviroc Sulfone
CAS:<p>Cenicriviroc Sulfone, a Cenicriviroc derivative, inhibits CCR2/CCR5 to block HIV entry into cells.</p>Fórmula:C41H52N4O5SForma y color:SolidPeso molecular:712.94GPX100 HCl
CAS:<p>GPX-100, a non-cardiotoxic doxorubicin analog, intercalates DNA and inhibits replication, repair, and protein synthesis.</p>Fórmula:C27H32ClNO10Forma y color:SolidPeso molecular:566Dioxolamycin
CAS:<p>Dioxolamycin is an antitumor antibiotic that inhibits the activity of L-1210 cells.</p>Fórmula:C11H15NO6Forma y color:SolidPeso molecular:257.24BXL0124
CAS:<p>BXL0124 is a gemini vitamin D analog which targets CD44-STAT3 signaling and inhibits breast cancer invasion.</p>Fórmula:C32H44F6O4Forma y color:SolidPeso molecular:606.68Pinselin
CAS:<p>Pinselin is a nitrogen-containing heterocyclic antibiotic with yeast-inhibiting properties.</p>Fórmula:C16H12O6Forma y color:SolidPeso molecular:300.263LGB-321 HCl
CAS:<p>LGB-321: potent, selective PIM kinase inhibitor, active against PIM2, halts diverse blood cancers' growth, orally effective in mice.</p>Fórmula:C23H23ClF3N5O2Forma y color:SolidPeso molecular:493.91Cedarmycin B
CAS:<p>Cedarmycin B exhibits activity against Candida, Cryptococcus neoformans, and Aspergillus fumigatus, with a minimum inhibitory concentration (MIC) ranging from 12.5 to 50 μg/mL.</p>Fórmula:C12H18O4Forma y color:SolidPeso molecular:226.269YM-202074
CAS:<p>YM-202074: Selective mGlu1 antagonist, binds allosteric site (Ki=4.8 nM), inhibits mGlu1 (IC50=8.6 nM).</p>Fórmula:C22H30N4O2SForma y color:SolidPeso molecular:414.56SphK1-IN-1
<p>SphK1-IN-1: SphK1 ATPase inhibitor, IC50=2.48 μM, potential for cancer research.</p>Fórmula:C22H22N6O2Forma y color:SolidPeso molecular:402.45MSK-195
CAS:<p>MSK-195 is an effective TRPV1 agonist.</p>Fórmula:C28H40N2O5Pureza:98%Forma y color:SolidPeso molecular:484.63Diatretyne Ⅰ
CAS:Diatretyne I (Diatretyne amide) exhibits mild activity against Gram-positive bacteria.Fórmula:C8H5NO3Forma y color:SolidPeso molecular:163.13TCMDC-136230
<p>TCMDC-136230 is a novel inhibitor of Plasmodium calcium kinetics with minimal inhibition of haemoglobin crystallisation.</p>Fórmula:C24H34N4O2SForma y color:SolidPeso molecular:442.62NSC 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:C26H20N4O2Forma y color:SolidPeso molecular:420.463STAT3-IN-7
CAS:<p>STAT3-IN-7, an orally active aryl sulfonamido azetidine compound, serves as a STAT3 inhibitor with anticancer activities.</p>Fórmula:C30H26F5N5O4SForma y color:SolidPeso molecular:647.62ACT-281959
CAS:<p>ACT-281959, a prodrug of ACT-246475, is a potent P2Y12 antagonist, better than Clopidogrel, effective orally, and in human trials.</p>Fórmula:C38H55N6O14PForma y color:SolidPeso molecular:850.8511-Deoxy-13-deoxodaunorubicin
CAS:<p>11-Deoxy-13-deoxodaunorubicin is an anthracycline antibiotic with activity against Gram-positive, Gram-negative bacteria, and tumors.</p>Fórmula:C27H31NO8Forma y color:SolidPeso molecular:497.537Hetrombopag olamine
CAS:<p>Hetrombopag olamine is a non-peptide thrombopoietin (TPO) receptor agonist with oral activity.</p>Fórmula:C29H36N6O7Pureza:98%Forma y color:SolidPeso molecular:580.63Henagliflozin
CAS:<p>Henagliflozin (SHR3824): an oral, selective SGLT2 inhibitor, weak on SGLT1.</p>Fórmula:C22H24ClFO7Forma y color:SolidPeso molecular:454.87Difeterol
CAS:<p>Difeterol is a biochemical.</p>Fórmula:C25H29NO2Forma y color:SolidPeso molecular:375.50Melithiazole B
CAS:<p>Melithiazol B is an antibiotic and a potent inhibitor of β-methoxyacrylate (MOA), with both antifungal and cytotoxic properties.</p>Fórmula:C20H24N2O4S2Forma y color:SolidPeso molecular:420.546Enpp-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:C17H19N5O3SForma y color:SolidPeso molecular:373.43AX15910
<p>AX15910 is a potent inhibitor of BRD4 and ERK5.</p>Fórmula:C32H38N6O3Forma y color:SolidPeso molecular:554.7STING agonist-7
<p>STING agonist-7 is an agonist of non-nucleotide STING that binds selectively to mouse STING but not human STING [1].</p>Fórmula:C17H12N4O4Forma y color:SolidPeso molecular:336.3RIPK1-IN-14
CAS:<p>RIPK1-IN-14 inhibits RIPK1 with 92 nM IC50 and reduces necrotic apoptosis in U937 cells.</p>Forma y color:SoildRTIOX-372
CAS:<p>RTIOX-372 is a potent and selective orexin-1 receptor antagonist.</p>Fórmula:C30H39N5O3Forma y color:SolidPeso molecular:517.66PX-316
CAS:<p>PX-316: AKT inhibitor, reduces Akt activity by 78% in HT-29 xenografts, effective against MCF-7 and HT-29 cancers, well-tolerated intravenously.</p>Fórmula:C28H57O10PForma y color:SolidPeso molecular:584.72AN-12-H5
CAS:<p>AN-12-H5 is an anti-enteroviral compound that targets the replication process of PV and EV71 viruses.</p>Fórmula:C24H23N3O4S3Forma y color:SolidPeso molecular:513.65CLR01 sodium
CAS:<p>CLR01 is a tweezer reducing α-synuclein in MSA, inhibits SOD1 in ALS, blocks Ebola/Zika, stabilizes proteins, and lessens mutant p53 toxicity.</p>Fórmula:C42H30Na2O8P2Forma y color:SolidPeso molecular:770.6211Piceid 6″-O-azelaic acid ester
<p>Piceid 6″-O-azelaic acid ester exhibited strong intracellular tyrosinase inhibition and decolorization activity.</p>Fórmula:C24H36O10Forma y color:SolidPeso molecular:484.54Leukotriene F-4 sulfone
CAS:<p>Leukotriene F-4 sulfone induces vascular permeability changes.</p>Fórmula:C28H44N2O10SForma y color:SolidPeso molecular:600.72BI-207524
CAS:<p>BI-207524 is a novel NS5B Thumb Pocket 1 Inhibitor with Improved Potency for the Potential Treatment of Chronic Hepatitis C Virus Infection.</p>Fórmula:C35H36ClN5O5Forma y color:SolidPeso molecular:642.14KFA1982
CAS:<p>KFA1982 is a novel and potent factor Xa inhibitor.</p>Fórmula:C28H34ClN3O9S2Forma y color:SolidPeso molecular:656.17KP 10614
CAS:<p>KP 10614 is a new prostacyclin analog that inhibits platelet-polymorphonuclear leukocyte interaction.</p>Fórmula:C23H32O4Forma y color:SolidPeso molecular:372.50AEP-IN-1
<p>APE-IN-1, a potent AEP inhibitor (IC50: 89 nM), aids Alzheimer's diagnosis and drug research.</p>Fórmula:C18H27N3O3Forma y color:SolidPeso molecular:333.43MEIS-IN-3
<p>MEIS-IN-3 is a potent inhibitor of MEIS.</p>Fórmula:C25H26N2O4Forma y color:SolidPeso molecular:418.48di-Val-L-dC
CAS:<p>Di-Val-L-dC, a reverse transcriptase inhibitor, is used potentially for treatment of HBV infection.</p>Fórmula:C19H31N5O6Pureza:98%Forma y color:SolidPeso molecular:425.48Formadicin A
CAS:<p>Formadicin A exhibits strong activity against various Pseudomonas, Proteus, and Alcaligenes bacteria.</p>Fórmula:C30H34N4O16Forma y color:SolidPeso molecular:706.608Epoxyquinomicin A
CAS:<p>Epoxyquinomicin A is an antibiotic isolated from Amycolatopsissp. It exhibits inhibitory activity against Micrococcus luteus, Bacillus subtilis, Pasteurella piscicida, and Staphylococcus aureus with MIC values of 3-12.5 µg/mL. Additionally, it shows cytotoxicity in cancer cells L1210, B16, and S180, with an IC50 of 2-8 µg/mL. Furthermore, Epoxyquinomicin A demonstrates anti-inflammatory effects in collagen-induced arthritis.</p>Fórmula:C14H10ClNO6Forma y color:SolidPeso molecular:323.685PZ-3022
CAS:<p>PZ-3022 is an orally active, conformational PanK activator that counteracts C3-CoA inhibition. In a mouse model of propionic acidemia, it elevates hepatic CoASH and C2-CoA levels while reducing C3-CoA, making it useful for studying mitochondrial defects in propionic acidemia.</p>Fórmula:C20H21N5OForma y color:SolidPeso molecular:347.41Halomicin D
CAS:<p>Halomicin D is an ansamycin-class antibiotic that exhibits activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C43H56N2O12Forma y color:SolidPeso molecular:792.911BRD-K25923209
CAS:<p>BRD-K25923209 is a novel inhibitor of BAF transcriptional repression.</p>Fórmula:C29H36N4O3Forma y color:SolidPeso molecular:488.621-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:C20H40N4O8Forma y color:SolidPeso molecular:464.554ZK824859 hydrochloride
<p>ZK824859 hydrochloride: oral uPA inhibitor with IC50 of 79 nM (uPA), 1580 nM (tPA), 1330 nM (fibrin).</p>Fórmula:C23H23ClF2N2O4Forma y color:SolidPeso molecular:464.89AS-1940477 hydrobromide
CAS:<p>AS-1940477 hydrobromide is a p38 mitogen-activated protein kinase (MAPK) inhibitor.</p>Fórmula:C24H23BrFN5O2Forma y color:SolidPeso molecular:512.38Dicetrorelix pamoate
CAS:<p>Cetrorelix pamoate is a synthetic decapeptide that acts as a GnRH antagonist, inhibiting the release of LH and FSH from the pituitary.</p>Fórmula:C163H200Cl2N34O34Forma y color:SolidPeso molecular:3250.49FXIa-IN-10
<p>FXIa-IN-10 is a potent, orally bioavailable inhibitor of Activator XI (FXIa) (Ki: 0.17 nM).</p>Fórmula:C23H18Cl2F3N9O2Forma y color:SolidPeso molecular:580.35MraY-IN-1
<p>MraY-IN-1 inhibits MraY (IC50: 140μM), fights E. coli K12, B. subtilis W23, P. fluorescens (MIC50: 7-46μg/ml), for antimicrobial research.</p>Fórmula:C35H46N3O5Forma y color:SolidPeso molecular:588.76P-gp modulator 3
<p>P-gp modulator 3 (Compound 37) is a potent, competitive, metabotropic P-glycoprotein (P-gp) modulator.</p>Fórmula:C31H37N3O5Forma y color:SolidPeso molecular:531.64Odiparcil
CAS:<p>Odiparcil is an orally active beta-d-thioxyloside analog.</p>Fórmula:C15H16O6SPureza:98%Forma y color:SolidPeso molecular:324.35Trk-IN-7
<p>Trk-IN-7 inhibits TRKA/B/C (IC50: 0.25-10 nM) & EML4-ALK (<15 nM), also targets various ALK mutations (IC50: 5-50 nM).</p>Fórmula:C18H17FN6O2Forma y color:SolidPeso molecular:368.36(6S)-CP-470711
CAS:<p>(6S)-CP-470711 (Compound 8) acts as an inhibitor of sorbitol dehydrogenase (SDH) in both humans and rats, exhibiting inhibitory concentrations (IC50) of 19 nM and 27 nM, respectively. Additionally, (6S)-CP-470711 has been shown to ameliorate diabetes in rats induced by Streptozotocin.</p>Fórmula:C18H26N6O2Forma y color:SolidPeso molecular:358.44DWN-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:C15H21Cl4N3OForma y color:SolidPeso molecular:401.15DAD dichloride
<p>DAD dichloride is a 3rd-gen photoelectric switch, blocks K+ channels, and helps in visual function research.</p>Fórmula:C26H42Cl2N6OForma y color:SolidPeso molecular:525.56BE-10988
CAS:<p>BE-10988 is a DNA topoisomerase (DNAtopoisomerase) inhibitor. It suppresses the growth of P388 murine leukemia cell lines that are resistant to Doxorubicin and Vinblastine by promoting the formation of DNA topoisomerase complexes.</p>Fórmula:C13H10N4O3SForma y color:SolidPeso molecular:302.31Lunacalcipol
CAS:<p>Lunacalcipol is used for the treatment of Secondary Hyperparathyroidism.</p>Fórmula:C28H42O4SForma y color:SolidPeso molecular:474.7RORγt modulator 5
CAS:<p>RORγt modulator 5, a potent RORγt modulator, exhibits a dissociation constant (K_i) of <100 nM.</p>Fórmula:C27H22F5N3O6SForma y color:SolidPeso molecular:611.54CGC 11144
CAS:<p>CGC 11144 is a Polyamine analogue inhibit tumor growth in vitro and in vivo.</p>Fórmula:C40H100Cl10N10Forma y color:SolidPeso molecular:1075.82KF-19418
CAS:<p>KF-19418 is a follicle stimulant that directly activates follicles in vitro and promotes hair growth in vivo.</p>Fórmula:C21H14N4OForma y color:SolidPeso molecular:338.36DC41
CAS:<p>DC41 is a CC-1065-based cancer drug, an antibody-linked DNA alkylator.</p>Fórmula:C37H34ClN5O4SPureza:98%Forma y color:SolidPeso molecular:680.2222-HDHA
CAS:<p>22-HDHA is an oxidation product of docosahexaenoic acid .</p>Fórmula:C22H32O3Forma y color:SolidPeso molecular:344.49Fosfazinomycin B
CAS:<p>Fosfazinomycin B exhibits activity against plant pathogenic fungi such as the rice blast pathogen (Xanthomonas oryzae).</p>Fórmula:C10H23N6O6PForma y color:SolidPeso molecular:354.3Artemisiane E
CAS:<p>Artemisiane E is a potent PI3K/AKT pathway inhibitor with an IC 50 of 8.9 μM .</p>Fórmula:C20H22O5Forma y color:SolidPeso molecular:342.39hCA IX-IN-1
<p>hCA IX-IN-1 inhibits human carbonic anhydrases I, II, IX, and XII with Ki values of 331.4, 28.4, 9.4, 17.8 nM and exhibits anticancer properties.</p>Fórmula:C19H18N2O3SForma y color:SolidPeso molecular:354.42Ganciclovir monophosphonate
CAS:<p>Ganciclovir monophosphate treats CMV, inhibiting replication in human/animal strains (IC50: 0.01μM).</p>Fórmula:C10H16N5O6PForma y color:SolidPeso molecular:333.24STING agonist-20
CAS:<p>STING agonist-20: potent, aids in XMT-2056 synthesis, used as a cancer vaccine adjuvant.</p>Fórmula:C36H39N11O8Forma y color:SolidPeso molecular:753.76FTO-IN-6
CAS:<p>FTO-IN-6 is a selective inhibitor of fat mass and obesity associated protein (FTO).</p>Fórmula:C14H12N4O6Forma y color:SolidPeso molecular:332.27L 156903
CAS:<p>L 156903 is a bioactive chemical. It also inhibits the binding of neurotensin to brain tissue.</p>Fórmula:C35H41N7O5SForma y color:SolidPeso molecular:671.81AL-GDa62
<p>AL-GDa62, a gastric cancer treatment lead, has EC50 of 3.2 μM (MCF10A-WT) and 2 μM (MCF10A-CDH1 -/-).</p>Fórmula:C24H28FN3OForma y color:SolidPeso molecular:393.5Theophylline EP impurity C
CAS:<p>Theophylline EP impurity C, an alkaloid with anti-bronchospasm activity, is employed to assess the purity and quality of compounds. This substance also holds potential clinical value in the management of asthma and chronic obstructive pulmonary disease (COPD).</p>Fórmula:C7H10N4O3Forma y color:SolidPeso molecular:198.18Propizepine
CAS:<p>Propizepine is a tricyclic antidepressant compound.</p>Fórmula:C17H20N4OForma y color:SolidPeso molecular:296.37GSK2945 hydrochloride
<p>GSK2945 HCl is a specific Rev-erbα antagonist, EC50: 21.5 μM (mouse), 20.8 μM (human), increases cholesterol 7α-hydroxylase.</p>Fórmula:C20H19Cl3N2O2SForma y color:SolidPeso molecular:457.8BM635 mesylate (1493762-74-5 free base)
<p>BM635 mesylate is an MmpL3 inhibitor with outstanding anti-mycobacterial activity (MIC50: 0.12 μM against M. tuberculosis H37Rv).</p>Fórmula:C26H33FN2O4SPureza:98%Forma y color:SolidPeso molecular:488.61Phenazostatin 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:C32H26N4O4Forma y color:SolidPeso molecular:530.57DMP-728 free base
CAS:<p>DMP-728 free base is a highly potent and selective GPIIbDIIa antagonist</p>Fórmula:C25H36N8O7Forma y color:SolidPeso molecular:560.60Retelliptine
CAS:Retelliptine, a DNA topoisomerase II inhibitor, is used potentially for the treatment of cancer.Fórmula:C25H32N4OPureza:98%Forma y color:SolidPeso molecular:404.55CI 992
CAS:<p>CI 992 is a novel potent inhibitor of primate renin.</p>Fórmula:C33H52N6O7S2Forma y color:SolidPeso molecular:708.93PD-1/PD-L1-IN-13
<p>PD-1/PD-L1-IN-13 is a potent immune checkpoint PD-1/PD-L1 inhibitor with an IC50 value of 10.2 nM for PD-1/PD- L1 interaction.PD-1/PD-L1-IN-13 promotes CD8+ T-</p>Fórmula:C36H34ClF2N3O9Forma y color:SolidPeso molecular:726.12Tilpisertib fosmecarbil
CAS:<p>Tilpisertib fosmecarbil is a potent inhibitor of serine/threonine kinases with anti-inflammatory properties.</p>Fórmula:C35H36ClN8O7PForma y color:SolidPeso molecular:747.149(R)-HETE
CAS:<p>9(R)-HETE, 50% of racemic mix, activates RXRγ 1.5x at 300 nM; identified by HPLC comparison.</p>Fórmula:C20H32O3Forma y color:SolidPeso molecular:320.47Terfluranol
CAS:<p>Terfluranol, a benzyl derivative, is utilized as an antitumor medication.</p>Fórmula:C17H17F3O2Forma y color:SolidPeso molecular:310.31Copper(II) ionophore I
CAS:Copper(II) ionophore I is an active compound.Fórmula:C26H44N2S4Forma y color:SolidPeso molecular:512.90Mifepristone methochloride
CAS:<p>Mifepristone methochloride is a glucocorticoid antagonist. This product will be sold for research use only.</p>Fórmula:C30H38ClNO2Forma y color:SolidPeso molecular:480.08PNU-140457
CAS:<p>PNU-140457 is a bio-active chemical.</p>Fórmula:C14H14FN5O3Forma y color:SolidPeso molecular:319.29Seldomycin factor 1
CAS:<p>Seldomycin factor 1 (XK 88-1) is an aminoglycoside antibiotic known for its broad-spectrum antibacterial activity.</p>Fórmula:C17H34N4O10Forma y color:SolidPeso molecular:454.473L 739749
CAS:<p>L 739749 is a CAAX peptidomimetic. It is also an inhibitor of farnesyl-protein transferase.</p>Fórmula:C24H41N3O6S2Pureza:98%Forma y color:SolidPeso molecular:531.73AKR1C3-IN-5
<p>AKR1C3-IN-5 inhibits AKR1C3, key in prostate/breast cancers, with MCF-7 cell IC50 of 9.6 μM.</p>Fórmula:C34H44N2O7Forma y color:SolidPeso molecular:592.72Naltalimide
CAS:<p>Naltalimide: µ-opioid receptor partial agonist, improves bladder storage by affecting spinal cord reflex.</p>Fórmula:C28H28N2O5Pureza:98%Forma y color:SolidPeso molecular:472.53Pamiparib maleate
CAS:<p>Pamiparib (BGB-290) is a selective PARP inhibitor that blocks DNA repair and promotes apoptosis.</p>Fórmula:C44H42F2N8O14Pureza:98%Forma y color:SolidPeso molecular:944.859TA-316
CAS:<p>Agent induces megakaryocytes/platelets from stem cells to treat thrombopenia.</p>Fórmula:C28H25BrN4O5S2Pureza:98%Forma y color:SolidPeso molecular:641.56Z57346765
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%Forma y color:SolidPeso molecular:294.35LMD-A
CAS:<p>LMD-A, also known as CCR8 antagonist LMD-A, is a CCR8 antagonist.</p>Fórmula:C27H32N4O4SForma y color:SolidPeso molecular:508.63UTPγS trisodium salt
CAS:<p>P2Y2 and P2Y4 receptor agonist</p>Fórmula:C9H12N2Na3O14P3SPureza:98%Forma y color:SolidPeso molecular:566.15Fudecalone
CAS:<p>Fudecalone is produced by the Penicillium strain FO-2030. It completely inhibits the coccidian parasite Eimeria Tenella that is resistant to Monensin.</p>Fórmula:C15H22O3Forma y color:SolidPeso molecular:250.33FTO-IN-1 TFA
<p>FTO-IN-1 TFA: FTO enzyme inhibitor, anti-obesity, IC50 < 1μM, potential cancer research tool.</p>Fórmula:C20H17Cl2F3N4O4Forma y color:SolidPeso molecular:505.27PDE4-IN-5
<p>PDE4-IN-5: potent PDE4 inhibitor, IC50 = 3.1 nM, superb skin penetration, anti-psoriasis effect.</p>Fórmula:C21H28N2O3Forma y color:SolidPeso molecular:356.46Mesulergine
CAS:<p>Mesulergine is metabolized into dopaminergic agonists.</p>Fórmula:C18H26N4O2SForma y color:SolidPeso molecular:362.49Thiazolo[5,4-c]pyridin-4(5H)-one
CAS:<p>Thiazolo[5,4-c]pyridin-4(5H)-one is a compound used for diagnostic imaging of TDP-43, in PET imaging of neurodegenerative diseases ALS、AD、FTD、LATE.</p>Fórmula:C22H22FN5O2SPureza:98.75%Forma y color:SolidPeso molecular:439.51Ambelline
CAS:<p>Ambelline has antitumor activity.</p>Fórmula:C18H21NO5Pureza:98%Forma y color:SolidPeso molecular:331.36Heme Oxygenase-1-IN-2
<p>Heme Oxygenase-1-IN-2 is a novel inhibitor of heme oxygenase-1 (HO-1), displaying potent antiproliferative activity in vitro, with an IC50 value of 0.95 μM.</p>Fórmula:C19H18ClN3OForma y color:SolidPeso molecular:339.82Bcl-2-IN-8
<p>Bcl-2-IN-8: potent, hinders cell growth/migration, induces apoptosis, promising in triple-negative breast cancer research.</p>Fórmula:C36H44O6Forma y color:SolidPeso molecular:572.734"-Demethylgentamicin C2
CAS:<p>4"-Demethylgentamicin C2 exhibits activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C19H39N5O7Forma y color:SolidPeso molecular:449.54Lactoquinomycin B
CAS:<p>Lactoquinomycin B is a quinone antibiotic with activity against Gram-positive bacteria and some Gram-negative bacteria, though its efficacy against Gram-negative species is weaker and it does not affect fungi. It inhibits various cell lines, including lymphoma L5178Y parental cells, doxorubicin-resistant cells, bleomycin-resistant cells, human leukemia K562 cells, and murine leukemia L-1210 and P388 cells, with ID50 (μg/mL) values of 0.43, 0.21, 0.19, 0.16, 0.2, and 0.12, respectively.</p>Fórmula:C24H27NO9Forma y color:SolidPeso molecular:473.473EP4 receptor antagonist 2
CAS:<p>EP4 receptor antagonist 2 (compound 2-13) is a potent agonist of the EP4 receptor (IC50: 7.8 nM) and has antitumour effects.</p>Fórmula:C27H29N3O5Forma y color:SolidPeso molecular:475.54AM-3189
CAS:<p>AM-3189: potent, selective GPR40 agonist with low CNS penetration, good pharmacokinetics, and efficacy mirroring AMG 837.</p>Fórmula:C27H25ClN2O3Forma y color:SolidPeso molecular:460.95Cuevaene 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:C21H22O5Forma y color:SolidPeso molecular:354.396Peridinin
CAS:<p>Peridinin is an exceptionally potent and membrane-embedded inhibitor of bilayer lipid peroxidation.</p>Fórmula:C39H50O7Forma y color:SolidPeso molecular:630.81CGC 11150
CAS:<p>CGC 11150 is a polyamine analogue inhibit tumor growth in vitro and in vivo.</p>Fórmula:C40H100Cl10N10Forma y color:SolidPeso molecular:1075.82FTO-IN-5
CAS:<p>FTO-IN-5 is a potent, selective inhibitor targeting the fat mass obesity-associated protein (FTO).</p>Fórmula:C23H18Cl2N6O6Forma y color:SolidPeso molecular:545.33TP3011
CAS:<p>TP3011 is a potent topoisomerase I inhibitor equipotent as SN38 and is an active metabolite of CH-0793076.</p>Fórmula:C26H26N4O5Pureza:98%Forma y color:SolidPeso molecular:474.51Aquayamycin
CAS:<p>Aquayamycin is an anthraquinone derivative and inhibitor of the enzyme tyrosine hydroxylase..</p>Fórmula:C25H26O10Forma y color:SolidPeso molecular:486.47Minnelide free acid
CAS:<p>Minnelide treats pancreatic cancer, hinders androgen-related prostate growth, shrinks tumors, and improves survival.</p>Fórmula:C21H27O10PForma y color:SolidPeso molecular:470.418(S),15(S)-DiHETE
CAS:<p>8(S),15(S)-DiHETE, from 15(S)-HETE's oxidation by 15-LO, triggers eosinophil movement at 1.5 μM; it counteracts pain and LTB4 effects.</p>Fórmula:C20H32O4Forma y color:SolidPeso molecular:336.47Polvitolimod
CAS:<p>Polvitolimod is a TLR7 agonist used to treat infectious disease and cancer.</p>Fórmula:C13H14FN5O4Forma y color:SolidPeso molecular:323.28Cicaprost
CAS:<p>Cicaprost (ZK 96480) is an IP agonist with artery relaxing effects; EC50 is 5.8 nM.</p>Fórmula:C22H30O5Forma y color:SolidPeso molecular:374.47LLS30
CAS:<p>LLS30 inhibits Gal-1, reduces its binding affinity, and may help treat advanced prostate cancer.</p>Fórmula:C34H33Cl4N5O3Forma y color:SolidPeso molecular:701.47Gallinamide A
CAS:Gallinamide A is a potent inhibitor of cathepsin L with an IC 50 value of 17.6 pM.Fórmula:C31H52N4O7Forma y color:SolidPeso molecular:592.77HbF inducer-1
<p>HbF inducer-1 is a fetal hemoglobin inducer which is orally bioavailable.</p>Fórmula:C18H19N3O3Forma y color:SolidPeso molecular:325.36Aristoforin
CAS:<p>Aristoforin is a SIRT1 and SIRT2 inhibitor that induces cell cycle arrest, shows potent antitumor effects, and inhibits lymphangiogenesis in vivo.</p>Fórmula:C37H54O6Forma y color:SolidPeso molecular:594.82PTP1B-IN-17
<p>PTP1B-IN-17, a benzimidazole derivative, inhibits PTP1B (Ki: 30.2 μM) and may help study type 2 diabetes.</p>Fórmula:C26H19N3O4SForma y color:SolidPeso molecular:469.51A 74273
CAS:<p>A 74273, a nonpeptidic and renin inhibitor, may be used to treat cardiovascular diseases due to renin inhibition.</p>Fórmula:C44H74N4O8Pureza:98%Forma y color:SolidPeso molecular:787.08RK-582
CAS:<p>RK-582: oral spiroindolinone tankyrase inhibitor, halts colon cancer growth in COLO-320DM mouse model.</p>Fórmula:C27H35FN6O3Forma y color:SolidPeso molecular:510.6SIK1 activator 1
CAS:<p>SIK1 activator 1 boosts SIK1 phosphorylation, reduces type 2 diabetes hyperglycemia, and inhibits liver gluconeogenesis.</p>Fórmula:C23H32O6Forma y color:SolidPeso molecular:404.50J-104132
CAS:<p>J-104132: potent human ETA/B antagonist; Ki: ETA=0.034nM, ETB=0.104nM; prevents ET-1 effects, ED50 i.v.=0.045mg/kg, p.o.=0.35mg/kg.</p>Fórmula:C31H33NO7Pureza:98%Forma y color:SolidPeso molecular:531.60TAM&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:C29H27F2N7O5Forma y color:SolidPeso molecular:591.57AKR1C3-IN-8
<p>AKR1C3-IN-8 (Compound 5) is an effective and selective AKR1C3 inhibitor (IC50=0.069 μM). AKR1C3-IN-8 has antitumor activity.</p>Fórmula:C23H20N4O3Forma y color:SolidPeso molecular:400.43Moflomycin
CAS:<p>Moflomycin is an anthracycline derivative. It exhibits a higher antileukemic activity compared to other anthracyclines.</p>Fórmula:C25H25IO10Pureza:98%Forma y color:SolidPeso molecular:612.36Monamycin 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:593.84Rafutrombopag
CAS:<p>Rafutrombopag is a thrombopoietin (TPO) agonist.</p>Fórmula:C25H22N4O5Forma y color:SolidPeso molecular:458.47CXCR4 probe 1
CAS:<p>CXCR4 probe 1, a specific PET tracer, targets CXCR4 with antagonist TN14003 (IC50: 6.9 nM), aiding in imaging CXCR4-related diseases and tumors.</p>Fórmula:C24H30FN5O4SForma y color:SolidPeso molecular:502.59Polyoxin E
CAS:<p>Polyoxin E is a nucleoside antifungal antibiotic that demonstrates significant effectiveness against rice sheath blight.</p>Fórmula:C17H23N5O13Forma y color:SolidPeso molecular:505.39Guanine-7-oxide
CAS:<p>Guanine-7-oxide (Guanine 7-N-oxide) is an antitumor antibiotic with antitumor and anti-Candida albicans activities. It inhibits the replication of viruses such as herpes virus, infectious hematopoietic necrosis virus (IHNV), and infectious pancreatic necrosis virus (IPNV). The compound also demonstrates significant activity against mouse L1210 leukemia cells.</p>Fórmula:C5H5N5O2Forma y color:SolidPeso molecular:167.126Monamycin G1
CAS:<p>Monamycin G1 is an ester-peptide antibiotic [esterpeptid]. It shows activity against Gram-positive bacteria.</p>Fórmula:C33H54ClN7O8Peso molecular:712.28MC4355
<p>MC4355 is a dual inhibitor of EZH2 and histone deacetylase (HDAC).</p>Fórmula:C30H36N4O5Forma y color:SolidPeso molecular:532.63ASP-8731
CAS:<p>ASP8731 is a selective inhibitor of BACH1 that prevents inflammation and vascular occlusion, and induces fetal hemoglobin in sickle cell disease.</p>Fórmula:C20H21N5O4Forma y color:SolidPeso molecular:395.41Piperazinomycin
CAS:<p>Piperazinomycin is an antifungal antibiotic, showing inhibitory activity against fungi and yeasts, especially against Trichophyton.</p>Fórmula:C18H20N2O2Forma y color:SolidPeso molecular:296.36Deldeprevir Na
CAS:<p>Deldeprevir Na is an Antiviral Polyprotein cleavage inhibitor. HCV NS3/4A inhibitor.</p>Fórmula:C45H55F2N6NaO8S2Forma y color:SolidPeso molecular:933.08Miyakamide B1
CAS:<p>Miyakamide B1 is an antibiotic with insecticidal properties, capable of inhibiting the growth of brine shrimp. It displays moderate activity against Xanthomonas bacteria and inhibits P388 cells with an IC50 of 8.8 μg/mL.</p>Fórmula:C31H32N4O4Forma y color:SolidPeso molecular:524.61BMS-751324
CAS:<p>BMS-751324: p38α MAPK inhibitor with carbamyl-methyl, esters, phosphate from HPA. Reduces rat arthritis swelling and TNFα.</p>Fórmula:C32H35N6O10PForma y color:SolidPeso molecular:694.63Mycoversilin
CAS:<p>Mycoversilin is an antibiotic with inhibitory activity against dermatophytes and plant pathogenic fungi, but it does not exhibit activity against yeasts and bacteria. It strongly inhibits protein synthesis.</p>Fórmula:C18H16O8Forma y color:SolidPeso molecular:360.315Irinotecan Carboxylate Sodium Salt
CAS:<p>Irinotecan Carboxylate Sodium Salt is a DNA topoisomerase inhibitor.</p>Fórmula:C33H39N4NaO7Forma y color:SolidPeso molecular:626.68WS-898
<p>WS-898 boosts paclitaxel efficacy in resistant cells by inhibiting ABCB1; IC50: SW620/Ad300 - 5.0 nM, KB-C2 - 3.67 nM, HEK293/ABCB1 - 3.68 nM.</p>Fórmula:C33H25N7OSForma y color:SolidPeso molecular:567.66NA 0362
CAS:<p>NA 0362 is a derivative of SF 2370 that inhibits smooth muscle contraction.</p>Fórmula:C28H26N4O4Forma y color:SolidPeso molecular:482.53MK-7445
CAS:<p>MK-7445 is a conformationally constrained inhibitor of non-nucleoside reverse transcriptase.</p>Fórmula:C21H13Cl2N7OForma y color:SolidPeso molecular:450.28NB-533
CAS:<p>NB-533 is a macrocyclic peptidic BACE-1 inhibitor.</p>Fórmula:C33H55N3O4Forma y color:SolidPeso molecular:557.81Efrapeptin F
CAS:<p>Efrapeptin F, from Tolypocladium fungi, inhibits mitochondrial complex V and targets nutrient-deprived tumor cells.</p>Fórmula:C82H141N18O16Forma y color:SolidPeso molecular:1635.11Griseolutein A
CAS:<p>Griseolutein A exhibits activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C17H14N2O6Forma y color:SolidPeso molecular:342.303Aeruginosin 98-B
CAS:<p>Aeruginosin 98-B, a protease inhibitor, effectively inhibits trypsin, plasmin, and thrombin with IC50 values of 0.6, 7.0, and 10.0 μg/mL, respectively.</p>Fórmula:C29H46N6O9SForma y color:SolidPeso molecular:654.78SSTR4 agonist 4
CAS:<p>SSTR4 agonist 4, potent in pain research, shows promise in rodent pain models, with potential for Alzheimer's due to hippocampus activity.</p>Fórmula:C19H26N4OForma y color:SolidPeso molecular:326.44GSK 932121
CAS:<p>GSK 932121: potent antimalarial, targets P. falciparum by inhibiting cytochrome bc1 in the electron transport chain.</p>Fórmula:C20H15ClF3NO4Pureza:98%Forma y color:SolidPeso molecular:425.79VEGFR-2-IN-5 hydrochloride
<p>VEGFR-2-IN-5 hydrochloride is an effective VEGFR2 inhibitor.</p>Fórmula:C19H25ClN8Forma y color:SolidPeso molecular:400.91MK-8318
CAS:<p>MK-8318 is an effective and selective antagonist of the CRTh2 receptor (Ki: 5.0 nM).</p>Fórmula:C27H26F4N2O5Pureza:98%Forma y color:SolidPeso molecular:534.5Istamycin Y0
CAS:<p>Istamycin Y0 is an aminoglycoside antibiotic found in *Streptomyces tenjimariensis* [ATCC 31603]. This compound exhibits weak antibacterial activity against only a limited range of bacteria.</p>Fórmula:C14H30N4O4Forma y color:SolidPeso molecular:318.41BMS-681
CAS:<p>BMS-681 is a CCR2 antagonist blocking chemokine binding, aiding control of inflammatory and neurodegenerative diseases.</p>Fórmula:C26H36F3N5OForma y color:SolidPeso molecular:491.59Basroparib
CAS:<p>Basroparib is an inhibitor of ribose polymerase (PARP) and has shown antitumour effects.</p>Fórmula:C18H21F2N7O3Forma y color:SolidPeso molecular:421.4TY 11223
CAS:<p>TY 11223: stable homoisocarbacyclin analog, potently inhibits platelet aggregation with lasting effect and selective activity.</p>Fórmula:C24H34O5Forma y color:SolidPeso molecular:402.52Fleephilone
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:C24H27NO7Forma y color:SolidPeso molecular:441.474Antiangiogenic agent 3
<p>Antiangiogenic agent 3 blocks HUVEC cell migration, chemotaxis, and lowers Src, cdc42, MAPK gene expression.</p>Fórmula:C19H20O7Forma y color:SolidPeso molecular:360.36Flavipucine
CAS:<p>Flavipucine (Flavipucin) is a glutarimide antibiotic found in the Aspergillus flavipes F-2090/7 strain. It exhibits antibacterial activity against Bacillus subtilis, possesses antiprotozoal properties, and demonstrates cytotoxic effects on various cancer cells.</p>Fórmula:C12H15NO4Forma y color:SolidPeso molecular:237.252Mycinamicin Ⅵ
CAS:<p>Mycinamicin VI is a macrolide antibiotic with antibacterial activity against Gram-positive bacteria.</p>Fórmula:C35H57NO11Forma y color:SolidPeso molecular:667.83Dictyopanine 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:C25H34O5Forma y color:SolidPeso molecular:414.53Nanaomycin E
CAS:<p>Nanaomycin E is an antibiotic with activity against Gram-positive bacteria and fungi.</p>Fórmula:C16H14O7Forma y color:SolidPeso molecular:318.2785-Deoxygentamicin C1
CAS:<p>5-Deoxygentamicin C1 exhibits activity against both gram-positive and gram-negative bacteria.</p>Fórmula:C21H43N5O6Forma y color:SolidPeso molecular:461.60Calpain Inhibitor-2
CAS:<p>Calpain Inhibitor-2: Lipophilic, moderates growth of A-375, B-16F1, PC-3 cancers, and hinders 80% DU-145 cell invasion.</p>Fórmula:C26H33N3O5SForma y color:SolidPeso molecular:499.62Anticancer agent 79
<p>Anticancer agent 79 (3d) has potent activity against breast cancer, with cytotoxic effects on T47-D, IC50=13.64±0.26μM.</p>Fórmula:C20H12F3NO5Forma y color:SolidPeso molecular:403.31eIF4A3-IN-6
CAS:<p>eIF4A3-IN-6 is a potent eIF4A inhibitor, potentially used for treating eIF4A-related diseases like cancer. (US20170145026A1)</p>Fórmula:C26H25N3O5Forma y color:SolidPeso molecular:459.49Cytosaminomycin B
CAS:<p>Cytosaminomycin B exhibits activity against Eimeria Tenella coccidia.</p>Fórmula:C26H37N5O8Forma y color:SolidPeso molecular:547.6013'-GMP
CAS:<p>3'-GMP is a nucleotide that can be isolated from the tubers of Helianthus tuberosus L. (Jerusalem artichoke).</p>Fórmula:C10H14N5O8PForma y color:SolidPeso molecular:363.221FTI-2628
CAS:<p>FTI-2628 is a novel inhibitor of protein farnesyltransferase (FT), inhibiting the growth of P. falciparum in red blood cells and suppressing parasitemia.</p>Fórmula:C31H34N4O3SForma y color:SolidPeso molecular:542.69Nanaomycin B
CAS:<p>Nanaomycin B is an antibiotic with activity against Gram-positive bacteria, mycobacteria, mycoplasma, and fungi.</p>Fórmula:C16H16O7Forma y color:SolidPeso molecular:320.294ADP-2341
<p>ADP-2341 is a soluble analog of FiVe1.</p>Fórmula:C24H29Cl2N5O3Forma y color:SolidPeso molecular:506.43Cystothiazole A
CAS:<p>Cystothiazole A exhibits antifungal properties, effectively inhibiting Candida albicans, Saccharomyces cerevisiae, and Aspergillus fumigatus with minimum inhibitory concentrations (MIC) of 0.4 μg/mL, 0.1 μg/mL, and 1.6 μg/mL, respectively. It also demonstrates inhibitory activity against human tumor cells such as HPT-116 and K562, with MIC values of 130 ng/mL and 110 ng/mL. However, it shows no antibacterial activity.</p>Fórmula:C20H26N2O4S2Forma y color:SolidPeso molecular:422.561RN941
CAS:<p>RN941 is a highly potent Bruton's tyrosine kinase (BTK) inhibitor.</p>Fórmula:C34H34FN7O5Pureza:98%Forma y color:SolidPeso molecular:639.68Lipohexin
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:C39H68N6O9Forma y color:SolidPeso molecular:764.992S-1033
CAS:<p>S-1033 is an FP receptor agonist.</p>Fórmula:C20H33NaO4Forma y color:SolidPeso molecular:360.4698Dup-714
CAS:<p>Dup-714 is a thrombin inhibitor.</p>Fórmula:C21H33BN6O5Pureza:98%Forma y color:SolidPeso molecular:460.33Arterolane maleate
CAS:<p>Arterolane, an adenosine triphosphatase inhibitor, is used potentially for the treatment of malaria.</p>Fórmula:C26H40N2O8Pureza:98%Forma y color:SolidPeso molecular:508.612Epicorazine A
CAS:<p>Epicorazine A exhibits activity against Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci (VRE), with a minimum inhibitory concentration (MIC) of 12.5-25 μg/mL. It is also effective against Candida albicans, showing an MIC of 25 μg/mL.</p>Fórmula:C18H16N2O6S2Forma y color:SolidPeso molecular:420.459Enprostil
CAS:<p>Enprostil: synthetic PGE2 analog, reduces gastric acid, protects mucosa, lowers post-meal gastrin, treats ulcers effectively and safely.</p>Fórmula:C23H28O6Pureza:98%Forma y color:SolidPeso molecular:400.46Tribenuron
CAS:<p>Tribenuron, a slow acting sulfonylurea herbicide, controls broadleaf weed.</p>Fórmula:C14H15N5O6SForma y color:SolidPeso molecular:381.36FTO-IN-4
CAS:<p>FTO-IN-4 is a potent and selective inhibitor of adiposity and obesity-associated protein (FTO).</p>Fórmula:C22H16Cl2N6O6Forma y color:SolidPeso molecular:531.31RDN2150
CAS:<p>RDN2150 (Compound 25), a ZAP-70 inhibitor with an IC50 of 14.6 nM, covalently binds to the C346 residue of ZAP-70, suppressing the expression of CD25 and CD69</p>Fórmula:C28H29ClN8O4Forma y color:SolidPeso molecular:577.03Monorden diacetate
CAS:<p>Monorden diacetate a Hsp90 Inhibitor. Monorden diacetate is a Promising Lead Compound for the Development of Novel Fungicides.</p>Fórmula:C22H21ClO8Forma y color:SolidPeso molecular:448.85Amdinocillin methylacetate
CAS:<p>Amdinocillin methylacetate is a Synthetic penicillin.</p>Fórmula:C18H27N3O4SForma y color:SolidPeso molecular:381.49Granaticin B
CAS:<p>Granaticin B inhibits the initial phase of RNA biosynthesis and exhibits activity against Gram-positive bacteria, mycobacteria (weak), and Trichomonas vaginalis, along with the ability to suppress tumor cells.</p>Fórmula:C28H30O12Forma y color:SolidPeso molecular:558.531L2H2-6OTD
CAS:<p>L2H2-6OTD is a telomerase inhibitor with G-quadruplex loops; IC50: 15 nM.</p>Fórmula:C30H30N10O8Forma y color:SolidPeso molecular:658.62Deoxyfuconojirimycin hydrochloride
CAS:<p>Deoxyfuconojirimycin hydrochloride acts as a specific competitive inhibitor targeting human liver α-L-fucosidase.</p>Fórmula:C6H14ClNO3Forma y color:SolidPeso molecular:183.63
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