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 37926 productos de "Otros inhibidores"
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SK&F 108361
CAS:<p>SK&F 108361 is a symmetric diol that binds HIV-1 protease symmetrically.</p>Fórmula:C24H48N6O6Forma y color:SolidPeso molecular:516.67Melanoxazal
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:167.16K252d
CAS:<p>K252d: indolocarbazole alkaloid in Nocardiopsis; inhibits PKC in rat brain and bovine heart phosphodiesterase.</p>Fórmula:C26H23N3O5Forma y color:SolidPeso molecular:457.48MDL-100173
CAS:<p>MDL-100173 is a dual angiotensin-converting enzyme (ACE)/neutral endopeptidase (NEP) inhibitor.</p>Fórmula:C24H26N2O4SForma y color:SolidPeso molecular:438.54Pparδ agonist 5
<p>Pparδ agonist 5 is a selective, orally active PPARδ agonist with an EC50 of 0.335 μM and better selectivity than GW0742.</p>Fórmula:C23H21F3N2O2SForma y color:SolidPeso molecular:446.49LMD-A
CAS:<p>LMD-A, also known as CCR8 antagonist LMD-A, is a CCR8 antagonist.</p>Fórmula:C27H32N4O4SForma y color:SolidPeso molecular:508.63WS-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:567.66Tribenuron
CAS:<p>Tribenuron, a slow acting sulfonylurea herbicide, controls broadleaf weed.</p>Fórmula:C14H15N5O6SForma y color:SolidPeso molecular:381.36ATM-3507 trihydrochloride (1861449-70-8 free base)
<p>ATM-3507 trihydrochloride is a potent tropomyosin inhibitor (IC50s: 3.83-6.84 μM in human melanoma cell lines).</p>Fórmula:C37H49Cl3FN5O2Pureza:98%Forma y color:SolidPeso molecular:721.17PS-519
CAS:<p>PS-519 is a human tissue plasminogen activator and proteasome inhibitor.</p>Fórmula:C12H19NO4Forma y color:SolidPeso molecular:241.2818-Deoxyherboxidiene
CAS:<p>18-Deoxyherboxidiene (RQN-18690A) inhibits angiogenesis, targeting SF3b in U2 snRNP spliceosome, affects HUVEC, useful for cancer research.</p>Fórmula:C25H42O5Forma y color:SolidPeso molecular:422.6Hymenidin
CAS:<p>Hymenidin, isolated from the Okinawan sponge Hymeniacidon sp., is a 5-hydroxytryptaminergic receptor antagonist and voltage-gated potassium channel inhibitor.</p>Fórmula:C11H12BrN5OPureza:96.85% - 99.52%Forma y color:SolidPeso molecular:310.15Faldaprevir sodium
CAS:<p>Faldaprevir sodium: HCV treatment, inhibits NS3/NS4A protease, P-glycoprotein, CYP3A4, UGT1A1.</p>Fórmula:C40H48BrN6NaO9SForma y color:SolidPeso molecular:891.81NRX-2663
CAS:<p>NRX-2663 boosts β-catenin binding to E3 ligase SCFβ-TrCP (Kd: 54.8 nM, EC50: 22.9 nM).</p>Fórmula:C20H13F3N2O5Forma y color:SolidPeso molecular:418.32Nurr1 agonist 1
<p>Nurr1 agonist 1 is an inverse agonist tool for the neuroprotective transcription factor Nurr1 which is an appealing target to treat neurodegenerative diseases.</p>Fórmula:C16H14N2O2Forma y color:SolidPeso molecular:266.29Plagiochilin A
CAS:<p>Plagiochilin A Inhibits Cytokinetic Abscission and Induces Cell Death</p>Fórmula:C15H14O7Forma y color:SolidPeso molecular:306.27BMS-961955
CAS:<p>BMS-961955 is an allosteric inhibitor of the hepatitis C virus NS5B polymerase.</p>Fórmula:C37H43FN4O4SForma y color:SolidPeso molecular:658.83Heparastatin
CAS:<p>Heparastatin is an inhibitor of heparanase.</p>Fórmula:C8H11F3N2O5Pureza:98%Forma y color:SolidPeso molecular:272.18Ac-ATS010-KE
CAS:<p>Ac-ATS010-KE is a novel Selective, irreversible, and Rapid Cell-Permeable Inhibitor of Human Caspase-3.</p>Fórmula:C43H41F5N6O12SForma y color:SolidPeso molecular:960.88AD5075
CAS:<p>AD5075 is a bioactive chemical.</p>Fórmula:C22H20N2O5SForma y color:SolidPeso molecular:424.47Thiomuscimol hydrobromide
CAS:<p>Thiomuscimol hydrobromide is an agonist of GABAA receptor.</p>Fórmula:C4H6N2OSPureza:98%Forma y color:SolidPeso molecular:130.17GC 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%Forma y color:SolidPeso molecular:449.5Antitrypanosomal agent 5
<p>Antitrypanosal agent 5 is a selective anti-trypanosomal agent that acts on T. brucei (IC50: 1 nM) and HEK293 cells (IC50: 483.3 μM).</p>Fórmula:C30H30N6O4SForma y color:SolidPeso molecular:570.66TREX1-IN-2
CAS:<p>TREX1-IN-2 (Compound 15B) serves as an inhibitor of Human TREX1, displaying an IC 50 value of less than 1.00 μM. Additionally, this compound demonstrates anticancer activity in vivo.</p>Fórmula:C28H34Cl2N4O4Forma y color:SolidPeso molecular:561.5Deoxyradicinin
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:C12H12O4Forma y color:SolidPeso molecular:220.221Diospyrin
CAS:<p>Diospyrin is a plant product that has significant inhibitory effect on the growth of Leishmania donovani promastigotes.</p>Fórmula:C22H14O6Forma y color:SolidPeso molecular:374.34Sannamycin K
CAS:<p>Sannamycin K is an aminoglycoside antibiotic with weak antibacterial activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C13H26N4O4Forma y color:SolidPeso molecular:302.37Anticancer agent 78
<p>Anticancer agent 78: anti-aromatase (IC50=0.9 μM), cytotoxic, potential in breast cancer research.</p>Fórmula:C19H14BrNO4Forma y color:SolidPeso molecular:400.22ODN 21158
CAS:<p>ODN 21158 is a potent, non-cytotoxic inhibitor of G-modified TLR3 and TLR9. ODN 21158 dose-dependently inhibits IFN-α secretion.</p>Forma y color:SolidHMGB1-IN-3
CAS:<p>HMGB1-IN-3 (compound E), a derivative of glycyrrhizic acid, exhibits potent inhibitory effects on HMGB1 (high mobility group protein 1). It is utilized in research related to intracerebral hemorrhage.</p>Fórmula:C31H46O4Forma y color:SolidPeso molecular:482.69AL-6556
CAS:<p>AL-6556 is a prostaglandin DP receptor agonist.</p>Fórmula:C20H33ClO5Forma y color:SolidPeso molecular:388.93SORT1-IN-1
CAS:<p>SORT1-IN-1 (compound 2) is a SORT1 inhibitor.</p>Fórmula:C17H13F3N2O4Forma y color:SolidPeso molecular:366.29THR-β agonist 5
CAS:<p>THR-β agonist 5 (compound 54) is a potent THR-β agonist, with an EC 50 of <50 nM [1].</p>Fórmula:C22H23N5O2Forma y color:SolidPeso molecular:389.45Polyoxin K
CAS:<p>Polyoxin K is a nucleoside antifungal antibiotic that exhibits significant effectiveness against rice sheath blight.</p>Fórmula:C22H30N6O13Peso molecular:586.51PAD2-IN-1 hydrochloride
<p>PAD2-IN-1 hydrochloride: potent, selective PAD2 inhibitor; 95x less on PAD4, 79x less on PAD3; benzimidazole derivative.</p>Fórmula:C25H30ClFN6O3Forma y color:SolidPeso molecular:517di-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:425.48ONL-1204
CAS:<p>ONL-1204 is a small molecule, CD95 antigen inhibitor (Fas inhibitor) being developed by ONL Therapeutics for the treatment of retinal detachment.</p>Fórmula:C71H100N18O16Forma y color:SolidPeso molecular:1461.6617β-HSD1-IN-1
<p>17β-HSD1-IN-1 (Compound 1) can be used in the non-small cell lung cancer (NSCLC) research.</p>Fórmula:C21H21NO3Forma y color:SolidPeso molecular:335.4GDC-6036-NH
CAS:<p>GDC-6036-NH is a precursor of compound 17a /b, which is a RAS inhibitor that can be used in cancer research.</p>Fórmula:C26H30ClF4N7OPureza:99.84%Forma y color:SolidPeso molecular:568.01Ro-51
CAS:<p>dual P2X3 and P2X2/3 antagonist</p>Fórmula:C17H23IN4O4Pureza:98%Forma y color:SolidPeso molecular:474.297β,16α-Dihydroxybufalin
CAS:<p>7β,16α-Dihydroxybufalin, a dihydroxylated derivative of bufalin, demonstrates cytotoxic properties against various cancer cell lines.</p>Fórmula:C24H34O6Forma y color:SolidPeso molecular:418.52FK-906 HCl
CAS:<p>FK-906 HCl is a human renin inhibitor used for the long-term treatment of patients with essential hypertension.</p>Fórmula:C40H64ClN7O7Forma y color:SolidPeso molecular:790.44AEP-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:333.43Salfredin C3
CAS:<p>Salfredin C3 is an inhibitor of aldose reductase (aldose reductase).</p>Fórmula:C16H15NO8Forma y color:SolidPeso molecular:349.292ZBH-1205
CAS:<p>ZBH-1205, a camptothecin derivative, shows strong antitumor effects via apoptosis, outperforming cpt-11 and sn38 in topoisomerase-1 inhibition.</p>Fórmula:C29H31N3O8Forma y color:SolidPeso molecular:549.57Neuraminidase-IN-7
<p>Neuraminidase-IN-7, a thiophene, inhibits neuraminidase (IC50 0.03 μM), showing promise for flu research.</p>Fórmula:C21H20N2O6SForma y color:SolidPeso molecular:428.46EBOV-GP-IN-1
<p>EBOV-GP-IN-1 (Compound 28) is a potent inhibitor of Ebola entry, acting on the Ebola virus envelope glycoprotein (EBOV-GP) (IC50: 0.05 μM).</p>Fórmula:C25H40ClN3O2Forma y color:SolidPeso molecular:450.06AS-1940477 hydrobromide
CAS:<p>AS-1940477 hydrobromide is a p38 mitogen-activated protein kinase (MAPK) inhibitor.</p>Fórmula:C24H23BrFN5O2Forma y color:SolidPeso molecular:512.38Kynapcin-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:C19H12O10Forma y color:SolidPeso molecular:400.293Everafenib
<p>Everafenib: potent BRAF inhibitor, crosses blood-brain barrier, hinders MAPK, effective on V600EBRAF cells, outperforms other drugs in trials.</p>Fórmula:C20H23ClFN5O2S2Forma y color:SolidPeso molecular:484.01GS-9160
CAS:<p>GS-9160 is a novel and potent inhibitor of human immunodeficiency virus type 1 (HIV-1) integrase (IN) that specifically targets the process of strand transfer.</p>Fórmula:C20H18FN3O4SForma y color:SolidPeso molecular:415.44PDE4-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:356.46Ekatetrone
CAS:<p>Ekatetrone displays activity against both Gram-positive and Gram-negative bacteria, with particularly strong inhibitory effects on Mycobacterium tuberculosis.</p>Fórmula:C19H13NO7Forma y color:SolidPeso molecular:367.309ROS1-IN-1
<p>ROS1-IN-1, a potent ROS1 kinase inhibitor, has an IC50 of 0.097 μM.</p>Fórmula:C17H15ClN6SForma y color:SolidPeso molecular:370.8623-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:C38H63NO12Forma y color:SolidPeso molecular:725.91Steroid sulfatase/17β-HSD1-IN-4
<p>Steroid sulfatase/17β-HSD1-IN-4 (compound 37) is a potent dual inhibitor of steroid sulfatase ( STS ) and 17β-hydroxysteroid dehydrogenase type 1 ( 17β HSD1 ).</p>Fórmula:C18H17N3O4S2Forma y color:SolidPeso molecular:403.48HOE-288
CAS:<p>HOE-288 is a converting enzyme (CE) inhibitor.</p>Fórmula:C27H38N2O5Forma y color:SolidPeso molecular:470.60Dexnebivolol
CAS:<p>Dexnebivolol (R67138), a ß-adrenergic antagonist, is Nebivolol's enantiomer with β1 blocking and vasodilation properties.</p>Fórmula:C22H25F2NO4Forma y color:SolidPeso molecular:405.433'-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:363.221Kigamicin 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:C40H45NO15Forma y color:SolidPeso molecular:779.78Metocurine chloride
CAS:<p>Metocurine: a muscle relaxant, not for kidney failure patients as it's kidney-excreted.</p>Fórmula:C40H48Cl2N2O6Forma y color:SolidPeso molecular:723.72Ro-24-4736
CAS:<p>Ro 24-4736 is an effective and selective platelet-activating factor antagonist.</p>Fórmula:C31H20ClN5OSPureza:98%Forma y color:SolidPeso molecular:546.04BW-10
CAS:<p>BW-10 potently inhibits bombesin evoked release of gastrointestinal hormones in vitro and in vivo.</p>Fórmula:C57H72N14O8Forma y color:SolidPeso molecular:1081.27Chelocardin
CAS:<p>Chelocardin exhibits activity against Gram-positive and Gram-negative bacteria.</p>Fórmula:C22H21NO7Forma y color:SolidPeso molecular:411.405Cremeomycin
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:C8H6N2O4Forma y color:SolidPeso molecular:194.144SENP2-IN-1
CAS:<p>SENP2-IN-1 selectively inhibits SENP2, SENP1, and SENP5 with low IC50 values; useful in cancer studies.</p>Fórmula:C32H29N3O5S2Forma y color:SolidPeso molecular:599.72Melanocin A
CAS:<p>Melanocin A is an inhibitor of melanin biosynthesis. It suppresses the synthesis of melanin and tyrosinase with an IC50 of 9.0 nM and MIC of 0.9 μM. Additionally, Melanocin A exhibits antioxidant properties.</p>Fórmula:C18H14N2O5Forma y color:SolidPeso molecular:338.31P2X7 receptor antagonist-1
<p>P2X7 receptor antagonist-1 is a purinergic P2X7 receptor antagonist with anti-neuroinflammatory effects.</p>Fórmula:C22H20F4N2O3Forma y color:SolidPeso molecular:436.4Methyl 5-thia-6,8,11,14-eicosatetraenoate
CAS:<p>Methyl 5-thia-6,8,11,14-eicosatetraenoate is a bioactive chemical.</p>Fórmula:C20H32O2SForma y color:SolidPeso molecular:336.53Chloronectrin
CAS:<p>Chloronectrin exhibits activity against Gram-positive bacteria.</p>Fórmula:C25H33ClO6Forma y color:SolidPeso molecular:464.979Milbemycin α11
CAS:<p>Milbemycin α11 (Meilingmycin A) is an antibiotic known for its ability to eliminate nematodes and mites.</p>Fórmula:C36H50O9Forma y color:SolidPeso molecular:626.78Piceid 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:484.54Leu-AMS R enantiomer
CAS:<p>Leu-AMS R enantiomer is the R enatiomer of Leu-AMS. Leu-AMS is a potent leucyl-tRNA synthetase (LRS) inhibitor that inhibits the bacteria growth.</p>Fórmula:C16H25N7O7SPureza:98%Forma y color:SolidPeso molecular:459.48Phellinsin
CAS:<p>Phellinsin selectively inhibits the activity of chitin synthase I and II, with IC50 values of 76 and 28 μg/mL, respectively. It also exhibits antimicrobial effects against pathogens such as anthracnose, rice blast fungus, Aspergillus fumigatus, and Trichophyton mentagrophytes, with a MIC ranging from 12.5 to 50 μg/mL.</p>Fórmula:C18H14O8Forma y color:SolidPeso molecular:358.30S24-14
CAS:<p>S24-14 serves as an effective anti-osteoporosis agent by inhibiting osteoclastogenesis, promoting osteoblast differentiation, and reducing bone resorption.</p>Fórmula:C19H12N2O3SForma y color:SolidPeso molecular:348.38Calcipotriol Impurity C
CAS:<p>Calcipotriol Impurity C is the impurity of Calcipotriol. Calcipotriol is a VDR-like receptors ligand.</p>Fórmula:C27H40O3Pureza:98%Forma y color:SolidPeso molecular:412.614TLR7/8 antagonist 1
<p>Compound 16c, an imidazoquinoline, is a TLR7/8 agonist; IC50: 3.91 μM (TLR7), 2.19 μM (TLR8); targets TLR-2050 for disease treatment.</p>Fórmula:C24H27N5O2Forma y color:SolidPeso molecular:417.5Melithiazole N
CAS:<p>Melithiazol N is an antibiotic. It acts as a β-methoxyacrylate (MOA) inhibitor with potent antidrug activity.</p>Fórmula:C20H24N2O5S2Forma y color:SolidPeso molecular:436.545Kigamicin A
CAS:<p>Kigamicin A 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:C34H35NO13Forma y color:SolidPeso molecular:665.64Milbemycin α13
CAS:<p>Milbemycin α13 (Meilingmycin B) is an antibiotic that is effective against nematodes and mites.</p>Fórmula:C37H52O9Peso molecular:640.80Gilvocarcin E
CAS:<p>Gilvocarcin E exhibits activity against Gram-positive bacteria and is capable of inhibiting Sarcoma 180 and P388 leukemia cells.</p>Fórmula:C27H28O9Forma y color:SolidPeso molecular:496.506AL-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:393.5Pyloricidin A2
CAS:<p>Pyloricidin A2 is an antibiotic effective against Helicobacter pylori, produced by Bacillus species HC-70. It exhibits strong anti-Helicobacter pylori activity but shows no activity against other bacteria and yeast.</p>Fórmula:C32H53N5O10Forma y color:SolidPeso molecular:667.79Deoxyfuconojirimycin hydrochloride
CAS:<p>Deoxyfuconojirimycin hydrochloride acts as a specific competitive inhibitor targeting human liver α-L-fucosidase.</p>Fórmula:C6H14ClNO3Forma y color:SolidPeso molecular:183.63DDCPPB-Glu
CAS:<p>DDCPPB-Glu is a 6-5 fused ring heterocycle antifolate that shows antitumor activity.</p>Fórmula:C22H27N5O5Pureza:98%Forma y color:SolidPeso molecular:441.48AVE-1330A free acid
CAS:<p>AVE-1330A free acid is a broad-spectrum non-beta-lactam beta-lactamase inhibitor.</p>Fórmula:C7H11N3O6SForma y color:SolidPeso molecular:265.24Pyrrolomycin E
CAS:<p>Pyrrolomycin E is a pyrrole-based antibiotic with activity against Gram-positive bacteria, Gram-negative bacteria, and fungi.</p>Fórmula:C10H5Cl3N2O3Forma y color:SolidPeso molecular:307.517TCMDC-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:442.62Ceclazepide
CAS:<p>Ceclazepide is an antagonist of cholecystokinin receptor.</p>Fórmula:C30H32N6O5Pureza:98%Forma y color:SolidPeso molecular:556.61L 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:671.81ZIKV-IN-4
<p>ZIKV-IN-4 is a low cytotoxic, acid-stable anti-ZIKV agent with an EC50 value of 3.49 μM. ZIKV-IN-4 exhibited potent inhibition of ZIKV NS5 MTase.</p>Fórmula:C33H37NO4Forma y color:SolidPeso molecular:511.65DMP 728
CAS:<p>DMP 728 is an antagonist of Glycoprotein IIb-IIIa.</p>Fórmula:C26H40N8O10SPureza:98%Forma y color:SolidPeso molecular:656.71Dicetrorelix 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:3250.49Antiviral agent 7
<p>Antiviral agent 7 is a peptide-based coating that kills viruses.</p>Fórmula:C29H31F2N3O6Forma y color:SolidPeso molecular:555.57Griseorhodin G
CAS:<p>Griseorhodin G is a quinone antibiotic with antitumor activity.</p>Fórmula:C25H18O12Peso molecular:510.40ZL-Pin13
CAS:<p>ZL-Pin13: potent Pin1 inhibitor (IC50: 67 nM), halts MDA-MB-231 cell growth, reduces Pin1 substrates.</p>Fórmula:C24H23ClN2O3SForma y color:SoildPeso molecular:454.97Freselestat
CAS:<p>Freselestat (ONO-6818) inhibits neutrophil elastase, reduces interleukin 8, C5B-9, and inflammation in cardiopulmonary bypass.</p>Fórmula:C23H28N6O4Forma y color:SolidPeso molecular:452.51CYP11B1-IN-2
<p>CYP11B1-IN-2 selectively inhibits human and rat CYP11B1 (IC50: 9/25 nM) orally to research cortisol-related diseases.</p>Forma y color:SolidAmidomycin
CAS:<p>Amidomycin is an antibiotic that primarily targets yeast.</p>Fórmula:C40H68N4O12Forma y color:SolidPeso molecular:796.99Ornoprostil
CAS:<p>Ornoprostil, a prostaglandin E1 analogue, acts as a mucosal protectant.</p>Fórmula:C23H38O6Pureza:98%Forma y color:SolidPeso molecular:410.54Epicorazine 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:420.459Butaprost
CAS:<p>Butaprost: EP2 receptor agonist, EC50=33 nM, Ki=2.4 μM (murine), reduces fibrosis via TGF-β/Smad2.</p>Fórmula:C24H40O5Pureza:98%Forma y color:SolidPeso molecular:408.57Tylophorinidine
CAS:<p>Tylophorinidine is an antifungal agent that has shown to inhibit cell growth.</p>Fórmula:C22H23NO4Forma y color:SolidPeso molecular:365.42AMG-222 tosylate
CAS:<p>AMG-222 tosylate is a DPP-IV inhibitor in clinical development for type II diabetes.</p>Fórmula:C39H47N9O6SForma y color:SolidPeso molecular:769.91GW-597901 cinnamate
CAS:<p>GW-597901 cinnamate is a long-acting beta(2)-agonist.</p>Fórmula:C34H46N2O8SForma y color:SolidPeso molecular:642.80RS 2135
CAS:<p>RS 2135 is a novel class I antiarrhythmic agent to inhibit ischemia-induced ventricular arrhythmias.</p>Fórmula:C18H21ClN2O2Pureza:98%Forma y color:SolidPeso molecular:332.83DS01080522
<p>DS01080522: PRKACA inhibitor, IC50: kinase 0.8 nM, CREB 66 nM; potential for cancer research.</p>Fórmula:C23H20Cl2N4O3Forma y color:SolidPeso molecular:471.34Keap1-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:C26H25F3N2O9SForma y color:SolidPeso molecular:598.54PD-1-IN-17 TFA
<p>PD-1-IN-17 TFA is a potent PD-1 inhibitor, blocking 92% of splenocyte growth at 100 nM.</p>Fórmula:C15H23F3N6O9Forma y color:SolidPeso molecular:488.37BILA 1906 BS
CAS:<p>BILA 1906 BS is an inhibitor of substrate analog protease.</p>Fórmula:C41H52N6O4SPureza:98%Forma y color:SolidPeso molecular:724.95Antioxidant agent-3
<p>Antioxidant agent-3 shows strong DPPH and ABTS+ radical scavenging (IC50: 26.58, 30.31 μM). Boosts ROS, SOD, GSH; lowers LDH in H2O2-exposed HepG2 cells.</p>Fórmula:C18H14O8Forma y color:SolidPeso molecular:358.3NUCC-555
CAS:<p>NUCC-555 is a first-in-class antagonist of activin. It opens a completely new approach to inhibiting the activity of TGF-beta receptor superfamily members.</p>Fórmula:C25H25N5O3Pureza:98%Forma y color:SolidPeso molecular:443.5Topoisomerase I inhibitor 8
CAS:<p>Topoisomerase I inhibitor 8, a hexacyclic analogue of camptothecin, is also a potent inhibitor of topoisomerase I and is toxic to tumour cells.</p>Fórmula:C24H21FN2O4Forma y color:SolidPeso molecular:420.43SAR107375
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:C24H30ClN5O5S2Forma y color:SolidPeso molecular:568.11Azirinomycin
CAS:<p>Azirinomycin exhibits activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C4H5NO2Forma y color:SolidPeso molecular:99.088Fonsartan free acid
CAS:<p>Fonsartan: Angiotensin receptor blocker, halts angiotensin II effects on rat vascular cells.</p>Fórmula:C26H32N4O5S2Pureza:98%Forma y color:SolidPeso molecular:544.69Guraxetan
<p>Guraxetan can be used in the synthesis of the antitumour drug Lutetium (177Lu) zadavotide Guraxetan.</p>Fórmula:C20H34N4O9Forma y color:SolidPeso molecular:474.51Bulgecin A
CAS:<p>Bulgecin A is an inhibitor of binuclear metallo-beta-lactamases and Lytic transglycosolase.</p>Fórmula:C16H29N3O14S2Forma y color:SolidPeso molecular:551.54Chitinovorin C
CAS:<p>Chitinovorin C is a β-lactam class antibiotic (antibiotic) that exhibits weak inhibitory activity against Gram-negative bacteria.</p>Fórmula:C15H20N4O8SForma y color:SolidPeso molecular:416.406AVE-1330A sodium
CAS:<p>AVE-1330A sodium is a beta-Lactamase inhibitor.</p>Fórmula:C7H10N3NaO6SForma y color:SolidPeso molecular:287.23IACS-8779 disodium
CAS:<p>IACS-8779 disodium: potent STING agonist, strong systemic anti-tumor effects, effective in melanoma model.</p>Fórmula:C21H23N9Na2O10P2S2Forma y color:SolidPeso molecular:733.52TTK inhibitor 3
CAS:<p>TTK inhibitor 3 is a potent and selective TTK (an essential spindle assembly checkpoint enzyme) inhibitor with an IC 50 value of 3.0 nM.</p>Fórmula:C42H49N9O3Forma y color:SolidPeso molecular:727.9Oiligodendrocyte differentiation promoter 1
CAS:<p>Oiligodendrocyte differentiation promoter 1 is a promoter of oiligodendrocyte differentiation .</p>Fórmula:C25H25Cl2NO5Pureza:98%Forma y color:SolidPeso molecular:490.38Trypanothione synthetase-IN-4
<p>Trypanothione synthetase-IN-4, an L. infantum inhibitor, has potent anti-leishmanicidal properties (EC50: 0.6 μM).</p>Fórmula:C29H52INO2Forma y color:SolidPeso molecular:573.63Schidigera-genin B
CAS:<p>Schidigera-genin B is a steroidal saponin that can be isolated from Yucca glauca. It exhibits mild antifungal activity.</p>Fórmula:C27H40O4Forma y color:SolidPeso molecular:428.604Anticancer agent 26
<p>Anticancer agent 26 is a promising candidate for cancer therapy and deserves further development.</p>Fórmula:C28H33NO5Forma y color:SolidPeso molecular:463.57CEP-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:689.20Protease-Activated Receptor-1 antagonist 1
<p>Compound 13 is a PAR-1 antagonist with a 3 nM IC50, useful for thrombosis and heart disease research.</p>Fórmula:C25H24F2N2O3Forma y color:SolidPeso molecular:438.47RIPK1-IN-26
CAS:<p>RIPK1-IN-26 is a potent inhibitor of Receptor-Interacting Serine/Threonine Kinase 1 (RIPK1), exhibiting anti-necrotic properties in cells. This compound demonstrates good metabolic stability and binding specificity in mice. RIPK1-IN-26 holds potential for development as a PET imaging probe and in the research of neurodegenerative diseases.</p>Fórmula:C15H20FNO2Forma y color:SolidPeso molecular:265.32BRD-K25923209
CAS:<p>BRD-K25923209 is a novel inhibitor of BAF transcriptional repression.</p>Fórmula:C29H36N4O3Forma y color:SolidPeso molecular:488.62SARS-CoV-2-IN-23
<p>SARS-CoV-2-IN-23 (compound GRL-0617) is an inhibitor of SARS-COV-2 papain-like protease (PLpro) (IC 50 = 2.3 μM) [1].</p>Fórmula:C21H22N2OForma y color:SolidPeso molecular:318.41L-739750
CAS:<p>L-739,750 is an inhibitor (FTI) of peptidomimetic farnesyltransferase.</p>Fórmula:C23H39N3O6S2Pureza:98%Forma y color:SolidPeso molecular:517.7MSK-195
CAS:<p>MSK-195 is an effective TRPV1 agonist.</p>Fórmula:C28H40N2O5Pureza:98%Forma y color:SolidPeso molecular:484.63DGY-08-097
CAS:<p>DGY-08-097: potent HCV NS3 degrader, low resistance risk, strong inhibition in cells, DC50 of 50nM at 4h.</p>Fórmula:C60H76N10O14Forma y color:SolidPeso molecular:1161.3Narbomycin
CAS:<p>Narbomycin exhibits activity against Gram-positive bacteria.</p>Fórmula:C28H47NO7Forma y color:SolidPeso molecular:509.675T-3861174
CAS:<p>T-3861174 is a prolyl tRNA synthetase (PRS) inhibitor, exhibiting significant in vitro anti-tumor activity with GCN2-ATF4 pathway activation.</p>Fórmula:C26H25FN6O2Forma y color:SolidPeso molecular:472.5118:0-LPS
CAS:<p>18:0-LPS (Lysophosphatidylserine C18:0) is an endogenous lipid identified during the oxidation of phospholipids. It holds potential for use in cardiovascular disease research.</p>Fórmula:C24H48NO9PForma y color:SolidPeso molecular:525.613PPO-IN-1
<p>PPO-IN-1 is a potent inhibitor of protoporphyrinogen IX oxidase (PPO) (Ki: 2.5 nM).</p>Fórmula:C18H10F3N3O4SForma y color:SolidPeso molecular:421.35JBJ-08-178-01
CAS:<p>JBJ-08-178-01, a mutant-selective tyrosine kinase inhibitor, targets (HER2) human epidermal growth factor receptor 2 and exhibits antitumoral activity. This compound not only diminishes HER2's kinase activity and protein levels through the induction of proteasomal degradation of the receptor but also shows promise in non-small-cell lung cancer research.</p>Fórmula:C31H30N8O3Forma y color:SolidPeso molecular:562.62PCSK9-IN-16
CAS:<p>PCSK9-IN-16, holds potential for research into hypercholesterolemia and other cardiovascular diseases [1].</p>Fórmula:C16H20N6O2S3Forma y color:SolidPeso molecular:424.56β-N-Acetyl-D-hexosaminidase-IN-1
<p>β-N-Acetyl-D-hexosaminidase-IN-1 is a newly discovered chemical compound that acts as an inhibitor for β-N-acetyl-D-hexosaminidase.</p>Fórmula:C18H13F2NO2SForma y color:SolidPeso molecular:345.36GSK1820795A
CAS:<p>GSK1820795A: Telmisartan analog, selective hGPR132a antagonist, blocks yeast activation by N-acylamides, angiotensin II antagonist, partial PPARγ agonist.</p>Fórmula:C35H34N8Forma y color:SolidPeso molecular:566.7Dermostatin A
CAS:<p>Dermostatin A is a polyene antibiotic with antifungal properties suitable for studying fungal infections.</p>Fórmula:C40H64O11Forma y color:SolidPeso molecular:720.93Sekdel sequence
CAS:<p>Sekdel sequence, as a signal, leads to retention of at least two proteins in the endoplasmic reticulum of animal cells.</p>Fórmula:C29H49N7O14Forma y color:SolidPeso molecular:719.74Endophenazine A
CAS:<p>Endophenazine A exhibits activity against Gram-positive bacteria and filamentous fungi such as Mucor and Penicillium, but demonstrates limited herbicidal effect on Lemna.</p>Fórmula:C18H16N2O2Forma y color:SolidPeso molecular:292.332OUN58101
CAS:<p>OUN58101, also MDK-8101/BI-D, is an RSV L-protein inhibitor with no formal name, first reported in patent WO 2005042530.</p>Fórmula:C32H36N6O6Forma y color:SolidPeso molecular:600.66BGC-638
CAS:<p>BGC-638, an analogue of BGC-945, is a thymidylate synthase inhibitor specifically transported into α-folate receptor (α-FR)–overexpressing tumors.</p>Fórmula:C32H33N5O9Forma y color:SolidPeso molecular:631.63Retelliptine
CAS:<p>Retelliptine, a DNA topoisomerase II inhibitor, is used potentially for the treatment of cancer.</p>Fórmula:C25H32N4OPureza:98%Forma y color:SolidPeso molecular:404.55L 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:531.73NNC-11-1585
CAS:<p>NNC-11-1585 is an M(1) and M(2) muscarinic acetylcholine receptor (mAChR) agonist.</p>Fórmula:C18H19N3OSForma y color:SolidPeso molecular:325.43H 218-54
CAS:<p>H 218-54 is a renin inhibitor.</p>Fórmula:C37H56N2O5SForma y color:SolidPeso molecular:640.92MRS2179 tetrasodium hydrate
<p>MRS2179 blocks turkey P2Y1 receptor (Kb 102 nM, pA2 6.99), affects platelet aggregation, and has varying IC50s on P2 receptors.</p>Fórmula:C11H15N5Na4O10P2Forma y color:SolidPeso molecular:576.21Naltalimide
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:944.8598-iso Prostaglandin F3α
CAS:<p>8-iso PGF3α is an isoprostane produced from the free-radical peroxidation of EPA.</p>Fórmula:C20H32O5Forma y color:SolidPeso molecular:352.47Hsp90-IN-16
<p>Hsp90-IN-16, a selective HSP90 inhibitor, targets HER2+ cancers with 6 μM IC50 in HCC1954 cells, blocking client proteins and inducing apoptosis.</p>Fórmula:C30H26FN3O6Forma y color:SolidPeso molecular:543.54Ambelline
CAS:<p>Ambelline has antitumor activity.</p>Fórmula:C18H21NO5Pureza:98%Forma y color:SolidPeso molecular:331.36G12Si-1
<p>G12Si-1 selectively binds and inhibits K-Ras(G12S) to block oncogenic signaling and nucleotide exchange.</p>Fórmula:C29H32ClN5O3Forma y color:SolidPeso molecular:534.05Steroid sulfatase-IN-4
<p>Steroid sulfatase-IN-4 irreversibly inhibits human STS with a 25 nM IC50, useful for endometriosis research.</p>Fórmula:C19H17ClN2O5SForma y color:SolidPeso molecular:420.87DI-404
CAS:<p>DI-404: Potent DCN1-UBC12 inhibitor, selectivity blocks cullin 3 neddylation, Kd=6.9 nM.</p>Fórmula:C35H45ClN6O6SPureza:98%Forma y color:SolidPeso molecular:713.29Chrymutasin C
CAS:<p>Chrymutasin C is a glycoside antitumor antibiotic with cytotoxic properties.</p>Fórmula:C39H43NO17Forma y color:SolidPeso molecular:797.755Zetomipzomib
CAS:<p>KZR-616: Immunoproteasome inhibitor targeting LMP7 (IC50: 39/57 nM) & LMP2 (IC50: 131/179 nM), potential in autoimmune disease research.</p>Fórmula:C30H42N4O8Forma y color:SolidPeso molecular:586.68PARP7-IN-12
CAS:<p>PARP7-IN-12, a potent inhibitor targeting PARP7, exhibits an IC50 of 7.836 nM. This compound is applicable in cancer research.</p>Fórmula:C23H27ClF3N5O5Forma y color:SolidPeso molecular:545.94ETX0282
CAS:<p>ETX0282, oral class A/C β-lactamase inhibitor, developed by Entasis with cefpodoxime for bacterial infections.</p>Fórmula:C13H18FN3O5Forma y color:SolidPeso molecular:315.30PDE4B/7A-IN-2
CAS:<p>5-HT1A/5-HT7 antagonist; 5-HT1A Ki=8 nM, 5-HT7 Ki=451 nM; PDE4B IC50=80.4 μM, PDE7A IC50=151.3 μM; stronger than escitalopram.</p>Fórmula:C25H35N3O2Forma y color:SolidPeso molecular:409.56FTO-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:332.27Leucomycin 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:C37H61NO14Forma y color:SolidPeso molecular:743.878BRD4-IN-9
CAS:<p>BRD4-IN-9, an orally active BRD4 inhibitor, demonstrates a potent IC50 of 9.4 nM. In a murine melanoma xenograft model, it effectively inhibits tumor growth.</p>Fórmula:C24H23N3O3Forma y color:SolidPeso molecular:401.46GSK2578999A
CAS:<p>GSK2578999A is a betulin derivative with antitumor activity.</p>Fórmula:C46H62ClNO7Pureza:98%Forma y color:SolidPeso molecular:776.44Tyk2-IN-10
CAS:<p>Tyk2-IN-10 acts as an inhibitor of the Tyrosine Kinase 2 (Tyk2)-mediated signaling pathway, which plays a role in inflammation regulation.</p>Fórmula:C25H27N5O3Forma y color:SolidPeso molecular:445.51SPR-00305
CAS:<p>SPR-00305 is a novel potent inhibitor of the mvfr pathway</p>Fórmula:C24H19ClN2O3Forma y color:SolidPeso molecular:418.87trans-Doxercalciferol
CAS:<p>trans-Doxercalciferol is an isomer of Doxercalciferol. Doxercalciferol is an activator of the Vitamin D receptor and prevents renal disease.</p>Fórmula:C28H44O2Pureza:98%Forma y color:SolidPeso molecular:412.65Streptonigrin (racemate)
CAS:<p>Streptonigrin: aminoquinone antibiotic; antitumor, antibacterial; blocks β-Catenin/Tcf, cytotoxic; alters hamster chromosomes; (-)-isomer, CAS#3930-19-6.</p>Fórmula:C25H22N4O8Forma y color:SolidPeso molecular:506.46Calphostin I
CAS:<p>Calphostins, from Cladosporium fungus, inhibit PKC. Notably, calphostin C is a potent biochemical tool.</p>Fórmula:C44H38O15Forma y color:SolidPeso molecular:806.76p38-α MAPK-IN-5
CAS:<p>p38-α MAPK-IN-5: potent p38α inhibitor, IC50s: 0.1 nM (α), 0.2 nM (β), 944 nM (γ), 4100 nM (δ); anti-inflammatory, promising for asthma/COPD research.</p>Fórmula:C37H49N11O2Forma y color:SolidPeso molecular:679.86FTO-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:531.31Resolvin E4
CAS:<p>RvE4, a bioactive lipid from eicosapentaenoic acid and synthesized by 15-LO, is anti-inflammatory and boosts efferocytosis in human macrophages.</p>Fórmula:C20H30O4Forma y color:SolidPeso molecular:334.45Adiaft
CAS:<p>Adiaftis a bioactive chemical.</p>Fórmula:C10H11IN2O4Forma y color:SolidPeso molecular:350.11Foroxymithine
CAS:<p>Foroxymithine is an inhibitor of angiotensin-converting enzyme.</p>Fórmula:C22H37N7O11Pureza:98%Forma y color:SolidPeso molecular:575.57KUSC-5037
<p>KUSC-5037 inhibits HIF-1 (IC50 = 1.2 μM) and mitochondrial complex V/FoF1ATP synthase.</p>Fórmula:C18H17F3N6O2Forma y color:SolidPeso molecular:406.13651Flurdihydroergotamine
CAS:<p>Flurdihydroergotamine, a serotonin 5HT1 receptor agonist, is used as an antimigraine drug.</p>Fórmula:C34H36F3N5O5Pureza:98%Forma y color:SolidPeso molecular:651.68SMP-797 HCl
CAS:<p>SMP-797 HCl, an ACAT (acyl-CoA-cholesterol acyltransferase) inhibitor, is used potentially for the treatment of Hyperlipidemia.</p>Fórmula:C34H44ClN5O4Pureza:98%Forma y color:SolidPeso molecular:622.20BW A868C
CAS:BW A868C is a potent, selective PGD2 antagonist and a BW245C analogue, inert to other prostaglandin receptors.Fórmula:C25H37N3O5Forma y color:SolidPeso molecular:459.58Celesticetin B
CAS:<p>Celesticetin B is an antibiotic primarily exhibiting antibacterial activity against Gram-positive microorganisms.</p>Fórmula:C21H38N2O8SForma y color:SolidPeso molecular:478.6MtDTBS-IN-1
<p>MtDTBS-IN-1 is a notably potent binder (K_D = 57 nM) and inhibitor (K_i = 5 μM) of MtDTBS.</p>Fórmula:C16H16N4O5Forma y color:SolidPeso molecular:344.32MSX-3 free acid
CAS:<p>MSX-3 free acid is an A2A adenosine receptor antagonist and a prodrug of MSX-2.</p>Fórmula:C21H23N4O7PForma y color:SolidPeso molecular:474.40Rafutrombopag
CAS:<p>Rafutrombopag is a thrombopoietin (TPO) agonist.</p>Fórmula:C25H22N4O5Forma y color:SolidPeso molecular:458.47Imolamine hydrochloride
CAS:<p>Imolamine hydrochloride is a blood platelet aggregation antagonist.</p>Fórmula:C14H21ClN4OForma y color:SolidPeso molecular:296.80E-3030 free acid
CAS:<p>E-3030 free acid, a PPAR agonist, lowers blood glucose, triglycerides, and insulin; boosts adiponectin; reduces apo C-III; and raises lipoprotein lipase.</p>Fórmula:C22H23ClFNO5Pureza:98%Forma y color:SolidPeso molecular:435.87YKL-05-093
CAS:<p>YKL-05-093 is a alt inducible kinase (SIK) inhibitor. YKL-05-093 increases bone formation and bone mass.</p>Fórmula:C35H40N6O4Forma y color:SolidPeso molecular:608.73TLR7/8 agonist 7
CAS:<p>TLR7/8 agonist 7 activates immune cells, useful in ISAC synthesis and immunity research.</p>Fórmula:C26H37N7O2Forma y color:SolidPeso molecular:479.62Mycelianamide
CAS:<p>Mycelianamide is an antibiotic effective against Gram-positive bacteria.</p>Fórmula:C22H28N2O5Forma y color:SolidPeso molecular:400.468GNTI TFA
CAS:<p>GNTI TFA is a selective kappa opioid receptor antagonist.</p>Fórmula:C31H31F6N5O7Forma y color:SolidPeso molecular:699.60Carpetimycin C
CAS:<p>Carpetimycin C exhibits strong activity against both Gram-positive and Gram-negative bacteria, including those that produce β-lactamase. It also has a powerful inhibitory effect on β-lactamase .</p>Fórmula:C14H20N2O6SForma y color:SolidPeso molecular:344.383ZK168281
CAS:<p>ZK168281 is a 1α,25(OH)2D3 analog, VDR antagonist with 0.1 nM Kd, and blocks receptor CoA interaction.</p>Fórmula:C32H46O5Pureza:98%Forma y color:SolidPeso molecular:510.70Tuvatidine
CAS:<p>Tuvatidine is a histamine 2 receptor antagonist.</p>Fórmula:C10H17N9O2S3Forma y color:SolidPeso molecular:391.5Benadrostin
CAS:<p>Benadrostin is a Poly(ADP-ribose) synthetase inhibitor with an IC50 of 35μM.</p>Fórmula:C8H5NO4Forma y color:SolidPeso molecular:179.13Espinomycin A3
CAS:<p>Espinomycin A3 is a 16-membered macrolide antibiotic (antibiotic) that exhibits activity against Gram-positive bacteria.</p>Fórmula:C40H65NO15Forma y color:SolidPeso molecular:799.942AZ12971554
<p>AZ12971554: Human thrombin inhibitor, Ki=0.3nM; APTT IC50=0.68µM; ECT IC50=0.16µM.</p>Fórmula:C20H17ClFN7O3Forma y color:SolidPeso molecular:457.85Vanin-1-IN-3
<p>Vanin-1-IN-3 (OMP-7) is a vanin-1 inhibitor with an IC 50 of 0.038 μM [1].</p>Fórmula:C17H22F3NO5Forma y color:SolidPeso molecular:377.36
