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 37921 productos de "Otros inhibidores"
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Harziphilone
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:C15H18O4Forma y color:SolidPeso molecular:262.301Mutatochrome
CAS:<p>Mutatochrome (Citroxanthin) is a compound found in plants.</p>Fórmula:C40H56OForma y color:SolidPeso molecular:552.872Barixibat
CAS:<p>Barixibat is a bile acid transport inhibitor.</p>Fórmula:C42H55N5O8Forma y color:SolidPeso molecular:757.91Pochonin D
CAS:<p>Pochonin D is an inhibitor of heat shock protein 90 (Hsp90) with antiviral and anti-inflammatory properties. It disrupts Hsp90, affecting the stability, folding, and assembly of viral proteins, thereby diminishing viral replication. Additionally, Pochonin D reduces the infiltration of inflammatory cells and decreases the secretion of inflammatory cytokines such as TNF-α and IL-1β, alleviating inflammatory responses. This compound shows potential for research in human rhinovirus (HRV) infections and cancer.</p>Fórmula:C18H19ClO5Forma y color:SolidPeso molecular:350.793Adiaft
CAS:<p>Adiaftis a bioactive chemical.</p>Fórmula:C10H11IN2O4Forma y color:SolidPeso molecular:350.11GG-43
<p>GG-43 is a potent inhibitor of LIN28. The IC50 value of GG-43 against human LIN28A is 4 μM [1].</p>Fórmula:C21H21NO3Forma y color:SolidPeso molecular:335.4Azicemicin 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:C23H25NO9Forma y color:SolidPeso molecular:459.446MEN-10354
CAS:<p>MEN-10354 is a less potent and less selective NK-2 tachykinin receptor antagonist compared to the linear analog, R 396.</p>Fórmula:C37H46N8O9Forma y color:SolidPeso molecular:746.81EP4 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:475.54GNE-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%Forma y color:SolidPeso molecular:537.53Nolpitantium Free Base
CAS:<p>Nolpitantium is a potent, selective NK1 receptor antagonist that inhibits substance P without affecting NK2/NK3 receptors.</p>Fórmula:C37H45Cl2N2O2Forma y color:SolidPeso molecular:620.67Trk-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:C18H16F2N6O2Forma y color:SolidPeso molecular:386.363,4-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:C9H10O4Forma y color:SolidPeso molecular:182.1734-Nitrochalcone
CAS:<p>4-Nitrochalcone (2-(4-Nitrobenzylidene)acetophenone) inhibits proteasomes and suppresses TNFα-induced NF-κB activity.</p>Fórmula:C15H11NO3Forma y color:SolidPeso molecular:253.25Seldomycin factor 2
CAS:<p>Seldomycin factor 2 (XK 88-2) is an aminoglycoside antibiotic with broad-spectrum antibacterial activity.</p>Fórmula:C12H26N4O5Forma y color:SolidPeso molecular:306.359BILA 1906 BS
CAS:BILA 1906 BS is an inhibitor of substrate analog protease.Fórmula:C41H52N6O4SPureza:98%Forma y color:SolidPeso molecular:724.95Gougerotin
CAS:<p>Gougerotin is an inhibitor of protein synthesis.</p>Fórmula:C16H25N7O8Forma y color:SolidPeso molecular:443.4120-Deoxysalinomycin
CAS:<p>20-Deoxysalinomycin primarily targets Gram-positive bacteria, with a particular effectiveness against poultry coccidia.</p>Fórmula:C42H70O10Forma y color:SolidPeso molecular:735.00PRN694
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%Forma y color:SolidPeso molecular:543.67Fudecalone
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:250.33Pradimicin T2
CAS:<p>Pradimicin T2 is an antibiotic with activity against filamentous fungi and yeast-like fungi.</p>Fórmula:C37H37NO19Forma y color:SolidPeso molecular:799.685MSX-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:474.40Antiallergic agent-1
<p>Antiallergic agent-1, an Src family kinase inhibitor, is a new and valuable lead compound with potential as an anti-allergic agent.</p>Fórmula:C27H19F6N5OForma y color:SolidPeso molecular:543.46NVP-CFC218
CAS:<p>NVP-CFC218 is a novel potent and selective p53-HDM2 inhibitor.</p>Fórmula:C37H45ClN4O4Forma y color:SolidPeso molecular:645.23G-4120
CAS:<p>G-4120 is a biochemical that has been shown to have a dose-dependent complete inhibition of arterial and venous thrombosis.</p>Fórmula:C26H36N8O11SForma y color:SolidPeso molecular:668.68KY-02327 acetate
<p>KY-02327 acetate inhibits Dvl-CXXC5, stabilizes Wnt/β-catenin signaling, and enhances osteoblast differentiation.</p>Fórmula:C22H31N3O6Forma y color:SolidPeso molecular:433.5BMS-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:491.59PARP1-IN-5
<p>PARP1-IN-5 is a potent, selective, orally active, low-toxicity PARP-1 inhibitor with an IC50 value of 14.7 nM. PARP1-IN-5 can be used in cancer research.</p>Fórmula:C25H24N2O5SForma y color:SolidPeso molecular:464.53YKL-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:608.732,3-dinor-11β-Prostaglandin F2α
CAS:<p>2,3-dinor-11β-Prostaglandin F2α (2,3-dinor-11β-PGF2α) was recovered from the urine of both normal monkeys and humans when infused with radiolabeled PGD2, where</p>Fórmula:C18H30O5Forma y color:SolidPeso molecular:326.43DNDI-8219
CAS:<p>DNDI-8219 is an antitubercular agent. It has potent antileishmanial effects.</p>Fórmula:C13H10F3N3O5Forma y color:SolidPeso molecular:345.23TCMDC-135051 TFA (2413716-15-9 free base)
<p>TCMDC-135051 TFA is a highly selective and potent inhibitor of protein kinase PfCLK3.</p>Fórmula:C31H34F3N3O5Pureza:98%Forma y color:SolidPeso molecular:585.61Griseolic 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:C14H15N5O7Forma y color:SolidPeso molecular:365.298DMGF
CAS:<p>DMGF, a biflavonoid from Taxus, induces apoptosis, autophagy, and inhibits B16F10 cell motility and MMP-2 expression, hindering melanoma metastasis.</p>Fórmula:C32H22O10Forma y color:SolidPeso molecular:566.51Ranakinin
CAS:<p>Ranakinin is a novel tachykinin receptor agonist; from the brain of frog, Rana ridibunda.</p>Fórmula:C62H95N17O15SForma y color:SolidPeso molecular:1350.59Hsp90-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:543.54AVE-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:265.24RSV-IN-5
CAS:<p>RSV-IN-5: Dual inhibitor for RSV fusion proteins, effective on wild-type A2 and D486N mutant with EC50s of 2.0 nM & 8.1 nM. Potent anti-RSV.</p>Fórmula:C28H37N7O2Forma y color:SolidPeso molecular:503.64NUCC-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:443.5PDE4B/7A-IN-1
CAS:<p>5-HT1A antagonist; Ki=8nM, Kb=0.04nM. PDE4B IC50=80.4μM; PDE7A IC50=151.3μM. Good biofilm penetration, stable, anticognitive, antidepressant.</p>Fórmula:C25H35N3O3Forma y color:SolidPeso molecular:425.56Arterolane
CAS:<p>Arterolane is an antimalarial compound. For against P. falciparum Ro73 and W2, the IC50s are both 1.1 nM.</p>Fórmula:C22H36N2O4Forma y color:SolidPeso molecular:392.53OM-153
CAS:<p>OM-153 blocks tankyrase 1 (IC50: 13 nM) and 2 (IC50: 2 nM), stifling WNT signaling and COLO 320DM cell growth.</p>Fórmula:C28H24FN7O2Forma y color:SolidPeso molecular:509.53SBI-581
<p>SBI-581: oral, potent TAO3 inhibitor, IC50=42nM, alters TKS5α at RAB11+ vesicles, blocks invadopodia, good mouse pharmacokinetics, anti-tumor.</p>Fórmula:C24H21N3O2Forma y color:SolidPeso molecular:383.44DAD
<p>DAD is an ion channel blocker (blocks voltage-gated potassium channels) and is a third generation photoelectric switch that responds to visible light.</p>Fórmula:C26H40N6OForma y color:SolidPeso molecular:452.64Zurletrectinib
CAS:<p>Zurletrectinib is a tyrosine kinase inhibitor with potential as an antineoplastic agent.</p>Fórmula:C19H19F2N7O2Forma y color:SolidPeso molecular:415.4Anticancer agent 16
<p>Anticancer agent 16 showed good cytotoxic effects on HCT-116 cell line (IC50: 8.55 μM), NCI-H460 cell line (IC50: 5.41 μM) and SKOV3 cell line (IC50: 6.4 μM).</p>Fórmula:C27H33N5O6Forma y color:SolidPeso molecular:523.58MCTR1
CAS:<p>MCTR1, a pro-resolving mediator derived from DHA, promotes tissue repair and reduces inflammation by enhancing phagocytosis and decreasing eicosanoids.</p>Fórmula:C32H47N3O9SForma y color:SolidPeso molecular:649.8(-)-Adenophorine
CAS:<p>(-)-Adenophorine is a moderate alpha-l-fucosidase inhibitor.</p>Fórmula:C8H17NO4Forma y color:SolidPeso molecular:191.22Antitrypanosomal 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:570.66Hypoglycemic agent 1
CAS:<p>Hypoglycemic agent 1 has an action for lowering blood sugar. It acts as a therapeutic and/or prophylactic agent for diabetes.</p>Fórmula:C25H24FN5O4Pureza:98%Forma y color:SolidPeso molecular:477.49VEGFR-2-IN-12
<p>VEGFR-2-IN-12 (compound 6g), a 2-oxoquinoxalinyl-1,2,4-triazole, is a potent inhibitor of VEGFR-2 (IC50: 0.037 μM). VEGFR-2-IN-12 has anti-tumour effects.</p>Fórmula:C22H24N6O3SForma y color:SolidPeso molecular:452.53MAP3K14-IN-173
CAS:<p>MAP3K14-IN-173 is a potent MAP3K14 kinase inhibitor.</p>Fórmula:C29H31N7O2Forma y color:SolidPeso molecular:509.60AX15910
<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:336.3Memnobotrin A
CAS:<p>Memnobotrin A is an antibiotic with inhibitory effects on the NCI-460, MCF7, and SF-268 cell lines.</p>Fórmula:C25H33NO5Forma y color:SolidPeso molecular:427.53CVS-1578
CAS:<p>CVS-1578 is a potent serine protease inhibitor, targeting the S2S3 thrombin and FXa subsites.</p>Fórmula:C20H30N6O5SForma y color:SolidPeso molecular:466.55BRD-K25923209
CAS:<p>BRD-K25923209 is a novel inhibitor of BAF transcriptional repression.</p>Fórmula:C29H36N4O3Forma y color:SolidPeso molecular:488.62PPARα/γ agonist 1
<p>PPARα/γ agonist 1 is a potent and dual PPARα/γ partial agonist which is a promising prototype for the research of dyslipidemia and diabetes.</p>Fórmula:C18H19NO2Forma y color:SolidPeso molecular:281.35MK-7128
CAS:<p>MK-7128 is a CB1 receptor inverse agonist.</p>Fórmula:C29H25ClF2N4O2Forma y color:SolidPeso molecular:534.98CV 5975
CAS:<p>CV 5975 is a nonsulfhydryl ACE inhibitor that was investigated for use in hypertension and heart failure.</p>Fórmula:C22H31N3O5SForma y color:SolidPeso molecular:449.56Cilengitide hydrochloride
CAS:<p>Cilengitide hydrochloride is a salt that may combat cancer by blocking specific integrins, disrupting cell interactions and angiogenesis.</p>Fórmula:C27H41ClN8O7Forma y color:SolidPeso molecular:625.12Sequoiaflavone
CAS:<p>Sequoiaflavone is a biflavone isolated from Ginkgo biloba.</p>Fórmula:C31H20O10Forma y color:SolidPeso molecular:552.48Taprostene
CAS:<p>Taprostene (CG-4203), a stable Prostacyclin analogue, protects endothelium and myocardium post-ischemia in cats, with minimal hemodynamic impact.</p>Fórmula:C24H30O5Forma y color:SolidPeso molecular:398.49SARS-CoV-2-IN-24
<p>SARS-CoV-2-IN-24 blocks PLpro, altering its shape and stopping virus replication—useful for SARS-CoV-2 research.</p>Fórmula:C27H30N4O5Forma y color:SolidPeso molecular:490.55Oiligodendrocyte differentiation promoter 1
CAS:<p>Oiligodendrocyte differentiation promoter 1 is a promoter of oiligodendrocyte differentiation .</p>Fórmula:C25H25Cl2NO5Pureza:98%Forma y color:SolidPeso molecular:490.38LLS30
CAS:<p>LLS30 inhibits Gal-1, reduces its binding affinity, and may help treat advanced prostate cancer.</p>Fórmula:C34H33Cl4N5O3Forma y color:SolidPeso molecular:701.47Trk-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:368.36PPARγ phosphorylation inhibitor 1
<p>PPARγ phosphorylation inhibitor 1 (Compound 10) is a potent PPARγ binding agent (IC50: 24 nM) with antidiabetic effects.</p>Fórmula:C22H14Cl2N2O4Forma y color:SolidPeso molecular:441.262-Hydroxygentamicin B1
CAS:<p>2-Hydroxygentamicin B1 is an aminoglycoside antibiotic that exhibits activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C20H40N4O11Forma y color:SolidPeso molecular:512.552Nanaomycin D
CAS:<p>Nanaomycin D is an antibiotic with antibacterial properties.</p>Fórmula:C16H12O6Forma y color:SolidPeso molecular:300.263LH secretion antagonist 1
CAS:<p>LH secretion antagonist 1 is an antagonist of luteinizing hormone secretion with analgesic activity.</p>Fórmula:C18H24ClNO2Pureza:98%Forma y color:SolidPeso molecular:321.84Kerriamycin C
CAS:<p>Kerriamycin C exhibits activity against Gram-positive bacteria and also inhibits Ehrlich ascites carcinoma.</p>Fórmula:C37H46O15Forma y color:SolidPeso molecular:730.752Antibiotic MA 144M2
CAS:<p>Antibiotic MA 144M2, an anthracycline glycoside, targets gram-positive bacteria and tumors, derived from Streptomyces and aclacinomycin A conversion.</p>Fórmula:C42H55NO16Forma y color:SolidPeso molecular:829.88Ribocil-C R enantiomer
<p>Ribocil-C R enantiomer is the R enantiomer of Ribocil-C. Ribocil-C is a highly selective bacterial riboflavin riboswitches inhibitor.</p>Fórmula:C21H21N7OSPureza:98%Forma y color:SolidPeso molecular:419.5MK-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:534.5β-Prumycin hydrochloride
CAS:<p>β-Prumycin hydrochloride is a carbohydrate antibiotic that exhibits antifungal properties and possesses mild antibacterial activity.</p>Fórmula:C8H19Cl2N3O4Forma y color:SolidPeso molecular:292.16Gunacin
CAS:<p>Gunacin is a quinone antibiotic that exhibits significant activity against Gram-positive bacteria, Gram-negative bacteria, and mycoplasmas.</p>Fórmula:C17H16O8Forma y color:SolidPeso molecular:348.304[R-(Z)]-4-Amino-3-chloro-2-pen-tenedioicacid
CAS:<p>[R-(Z)]-4-Amino-3-chloro-2-pentenedioic acid inhibits Micrococcus luteus.</p>Fórmula:C5H6ClNO4Forma y color:SolidPeso molecular:179.56Antcin B
CAS:<p>Antcin B is an inhibitor of SARS-CoV-2 3-chymotrypsin-like protease (3CL Pro). It interacts with several crucial amino acid residues of 3CL Pro, including Leu141, Asn142, Glu166, and His163, through hydrogen bonding, salt bridges, and hydrophobic interactions, thereby inhibiting its activity. This inhibition blocks the cleavage of viral polyproteins and suppresses the replication of the SARS-CoV-2 virus within host cells. Antcin B shows potential for research in the context of COVID-19.</p>Fórmula:C29H40O5Forma y color:SolidPeso molecular:468.625Chrymutasin A
CAS:<p>Chrymutasin A is a glycoside antitumor antibiotic, known for its cytotoxic properties.</p>Fórmula:C33H33NO13Forma y color:SolidPeso molecular:651.614Dermostatin A
CAS:<p>Dermostatin A is a polyene antibiotic with antifungal properties suitable for studying fungal infections.</p>Fórmula:C40H64O11Forma y color:SolidPeso molecular:720.93Polyoxin A
CAS:<p>Polyoxin A is a nucleoside-based antifungal antibiotic.</p>Fórmula:C23H32N6O14Forma y color:SolidPeso molecular:616.532Neihumicin
CAS:<p>Neihumicin exhibits resistance against the yeast Saccharomyces cerevisiae (ATCC 9763) and the mold Penicillium italicum (Wehmer), but it does not show resistance to bacteria.</p>Fórmula:C19H16N2O2Forma y color:SolidPeso molecular:304.342Cryptosporiopsin
CAS:<p>Cryptosporiopsin can be isolated from strains of Cryptosporiopsis sp. and Sporormia affinis. It exhibits antimicrobial activity against various basidiomycetes, alga fungi, ascomycetes, and glaucomycetes responsible for wood decay. Additionally, it inhibits the germination of Phytophthora potatoes spores. Cryptosporiopsin also shows some activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C10H10Cl2O4Forma y color:SolidPeso molecular:265.09Cystothiazole 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:422.561Resorcinomycin B
CAS:<p>Resorcinomycin B is an antibiotic found in [Streptoverticillum roseoverticillatum].</p>Fórmula:C13H18N4O5Forma y color:SolidPeso molecular:310.306Menoxymycin A
CAS:<p>Menoxymycin A is an antibiotic with cytotoxic properties. It inhibits the growth of KB and N18-RE-105 cells, with IC50 values of 0.86 μM and 0.14 μM, respectively.</p>Fórmula:C24H27NO9Forma y color:SolidPeso molecular:473.473GSK866
CAS:<p>GSK866 is a selective glucocorticoid receptor agonist (SEGRA).</p>Fórmula:C23H21Cl2F4N5O3Forma y color:SolidPeso molecular:562.342-Hydroxybutirosin
CAS:<p>2-Hydroxybutirosin is an antibiotic that can be found in Bacillus circulans.</p>Fórmula:C21H41N5O13Forma y color:SolidPeso molecular:571.576MB-07344 sodium
<p>"MB-07344 sodium is a TR-β agonist with a 2.17 nM Ki, boosts Atorvastatin's cholesterol-lowering effects in various animals."</p>Fórmula:C19H25NaO5PPureza:98%Forma y color:SolidPeso molecular:387.36Roselipin 1A
CAS:<p>Roselipin 1A inhibits diacylglycerol acyltransferase (DGAT) in rats.</p>Fórmula:C40H72O14Forma y color:SolidPeso molecular:776.991Dihydrocompactin
CAS:<p>Dihydrocompactin is an antifungal metabolite derived from Penicillium citrinum and acts as an inhibitor of 3-hydroxy-3-methylglutaryl coenzyme-A reductase (HMG-CoA reductase).</p>Fórmula:C23H36O5Forma y color:SolidPeso molecular:392.529Gilvusmycin
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:C38H34N6O8Forma y color:SolidPeso molecular:702.712Pilatin
CAS:<p>Pilatin exhibits inhibitory effects on both bacteria and fungi, and it strongly suppresses the incorporation of thymidine and uridine into DNA and RNA in Ehrlich ascites tumor cells.</p>Fórmula:C21H26O7Forma y color:SolidPeso molecular:390.427Pacidamycin 5T
CAS:<p>Pacidamycin 5T is found in the bacterium Streptomyces coeruleorubidus [NRRL 18370].</p>Fórmula:C36H44N8O12Forma y color:SolidPeso molecular:780.78Sulprostone
CAS:<p>EP3 and EP1 receptor agonist</p>Fórmula:C23H31NO7SPureza:98%Forma y color:White To Off-White SolidPeso molecular:465.56Parimycin
CAS:<p>Parimycin exhibits activity against Gram-positive and Gram-negative bacteria, as well as tumors, but shows no efficacy against fungi. It inhibits tumor cells such as GXF 251L, H640, LXFA 629L, MCF-7, and MEXF 514L, with an IC70 range of 0.9-6.7 μg/mL.</p>Fórmula:C22H20O7Forma y color:SolidPeso molecular:396.3916-Hydroxyroridin L-2
CAS:<p>16-Hydroxyroridin L-2 is a member of the verrucarin subclass of antibiotics with antitumor properties.</p>Fórmula:C29H38O10Forma y color:SolidPeso molecular:546.606Micacocidin B
CAS:<p>Micacocidin B is an antibiotic that exhibits exceptional activity against Mycoplasma species.</p>Fórmula:C27H37CuN3O4S3Forma y color:SolidPeso molecular:627.34Cytochalasin M
CAS:<p>Cytochalasin M exhibits various biological activities, including reversible inhibition of cytoplasmic division and the suppression of both endocytosis and exocytosis in macrophages.</p>Fórmula:C30H37NO6Forma y color:SolidPeso molecular:507.618Carmegliptin dihydrochloride
CAS:<p>Carmegliptin dihydrochloride (RG-1579, RO4876904) is a salt of Camegliptin, a DPP-4 inhibitor for type 2 diabetes.</p>Fórmula:C20H30Cl2FN3O3Forma y color:SolidPeso molecular:450.38Fluvirucin A1
CAS:<p>Fluvirucin A1 is a novel antibiotic effective against the Influenza A virus.</p>Fórmula:C23H44N2O5Forma y color:SolidPeso molecular:428.61Eulicin
CAS:<p>Eulicin is an antifungal agent that inhibits human immunodeficiency virus (HIV) infection and replication. It demonstrates broad-spectrum activity against both Gram-positive and Gram-negative bacteria and can be found in Streptomyces.</p>Fórmula:C24H52N8O2Forma y color:SolidPeso molecular:484.722hCA 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:354.42Herbimycin B
CAS:<p>Herbimycin B, an ansamycin antibiotic, functions as an inhibitor of Src family kinases. It exhibits herbicidal effects on most monocotyledonous and dicotyledonous plants and can inhibit the activity of tobacco mosaic virus (TMV), HeLa cells, and Ehrlich cells.</p>Fórmula:C29H40N2O7Forma y color:SolidPeso molecular:528.637Exophilin A
CAS:<p>Exophilin A is an antibiotic that exhibits activity against Gram-positive bacteria.</p>Fórmula:C30H56O10Forma y color:SolidPeso molecular:576.76S-1033
CAS:<p>S-1033 is an FP receptor agonist.</p>Fórmula:C20H33NaO4Forma y color:SolidPeso molecular:360.4698SLN124
<p>SLN124, a GalNAc-siRNA targeting TMPRSS6, may normalize iron balance by restoring ferroregulation.</p>Forma y color:SolidMesulergine
CAS:<p>Mesulergine is metabolized into dopaminergic agonists.</p>Fórmula:C18H26N4O2SForma y color:SolidPeso molecular:362.49ZK159222
CAS:<p>ZK159222 is an effective 1α,25-(OH)2D3 receptor (VDR) agonist. ZK159222 has a partial agonistic character.</p>Fórmula:C32H48O5Pureza:98%Forma y color:SolidPeso molecular:512.72Dykellic acid
CAS:<p>Dykellic acid is a RhoA inhibitor. It can suppress the migration and motility of B16 cells and inhibit the tubular formation of HUVECs. Dykellic acid shows potential for use in cancer research.</p>Fórmula:C14H16O4Forma y color:SolidPeso molecular:248.2743-O-Demethylmonensin A
CAS:<p>3-O-Demethylmonensin A is a polyether antibiotic produced by Streptomyces cinnamonensis (strain LO-63).</p>Fórmula:C35H60O11Forma y color:SolidPeso molecular:656.84Enactin Ia
CAS:<p>Enactin Ia is found in Streptomyces roseoviridis and exhibits mild antibacterial activity.</p>Fórmula:C20H38N2O6Forma y color:SolidPeso molecular:402.526SAR107375
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:568.11Phencomycin
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:C15H10N2O4Forma y color:SolidPeso molecular:282.251Salfredin C1
CAS:<p>Salfredin C1 is an inhibitor of aldose reductase.</p>Fórmula:C13H11NO6Forma y color:SolidPeso molecular:277.229(S)-5-hydroxy-6-methoxy Duloxetine maleate
<p>(S)-5-hydroxy-6-methoxy Duloxetine, an active metabolite of the (S)-duloxetine, functions as a serotonin (5-HT) and norepinephrine reuptake inhibitor.</p>Fórmula:C19H21NO3S·C4H4O4Forma y color:SolidPeso molecular:459.51Monamycin H1
CAS:<p>Monamycin H1 is an ester peptide antibiotic that exhibits activity against Gram-positive bacteria.</p>Fórmula:C34H56ClN7O8Forma y color:SolidPeso molecular:726.30Salfredin C3
CAS:<p>Salfredin C3 is an inhibitor of aldose reductase (aldose reductase).</p>Fórmula:C16H15NO8Forma y color:SolidPeso molecular:349.292Coriolin 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:C23H36O6Forma y color:SolidPeso molecular:408.528Leucomycin A6
CAS:<p>Leucomycin A6 effectively combats Gram-positive bacteria.</p>Fórmula:C41H67NO14Forma y color:SolidPeso molecular:797.969Coriolin 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:C15H20O5Forma y color:SolidPeso molecular:280.31614,15-dehydro Leukotriene B4
CAS:<p>LTB4 is a leukocyte-activating fatty acid via 5-lipoxygenase. Two receptors, BLT1 and BLT2, bind it. 14,15-dehydro LTB4 is a stronger BLT1 antagonist.</p>Fórmula:C20H30O4Forma y color:SolidPeso molecular:334.45Bacithrocin B
CAS:<p>Bacithrocin B is a thrombin inhibitor that suppresses the activity of thrombin, Factor Xa, trypsin, and papain, with IC50 values of 84 μM, 17 μM, 1.7 μM, and 0.02 μM, respectively.</p>Fórmula:C19H29N5O3Forma y color:SolidPeso molecular:375.4655-Deoxygentamicin C1
CAS:<p>5-Deoxygentamicin C1 exhibits activity against both gram-positive and gram-negative bacteria.</p>Fórmula:C21H43N5O6Forma y color:SolidPeso molecular:461.60Glidobactin G
CAS:<p>Glidobactin G is an antitumor antibiotic with activity against pathogenic fungi and yeasts. Additionally, Glidobactin G prolongs the survival time of mice inoculated with leukemia P388 cells.</p>Fórmula:C27H44N4O7Forma y color:SolidPeso molecular:536.661RIP1 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%Forma y color:SolidPeso molecular:461.99-cis-13,14-Dihydroretinoic acid
CAS:<p>9-cis-13,14-Dihydroretinoic acid (9CDHRA) is a selective retinoid X receptor (RXR) agonist with a Kd of 90 nM. It can ameliorate memory deficits caused by impaired RXR signaling in vivo. This compound shows potential for research in the fields of neuroscience and metabolic diseases.</p>Fórmula:C20H30O2Forma y color:SolidPeso molecular:302.451Curvulic acid
CAS:<p>Curvulic acid exhibits relatively weak activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C11H12O6Forma y color:SolidPeso molecular:240.209Carzinophillin A
CAS:<p>Carzinophillin A exhibits inhibitory effects on both ascites carcinoma and Yoshida sarcoma.</p>Fórmula:C31H33N3O11Forma y color:SolidPeso molecular:623.607Dynemicin P
CAS:<p>Dynemicin P is an antibiotic.</p>Fórmula:C28H21NO9Forma y color:SolidPeso molecular:515.47Monamycin I
CAS:<p>Monamycin I is an ester peptide antibiotic with activity against Gram-positive bacteria.</p>Fórmula:C35H58ClN7O8Forma y color:SolidPeso molecular:740.33FR-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:C14H15N3O6Forma y color:SolidPeso molecular:321.29Gerfelin
CAS:<p>Gerfelin inhibits geranylgeranyl pyrophosphate synthase (GGPP synthase) activity, with an IC50 of 3.5 μg/mL.</p>Fórmula:C15H14O6Forma y color:SolidPeso molecular:290.268Pyripyropene B
CAS:<p>Pyripyropene B is a potent inhibitor of acyl-CoA:cholesterol acyltransferase 2 (ACAT2). It effectively inhibits acyl-CoA:cholesterol acyltransferase with an IC50 of 117 nM.</p>Fórmula:C32H39NO10Forma y color:SolidPeso molecular:597.653SLC4101431
<p>SLC4101431 is a potent SphK2 inhibitor with Ki value of 90 nM.</p>Fórmula:C29H28ClN7OSForma y color:SolidPeso molecular:558.1Dihydrobisdechlorogeodin
CAS:<p>Dihydrobisdechlorogeodin, produced by the fungus strain [FO-4712] of the genus Acremonium, serves as a herbicide.</p>Fórmula:C17H16O7Forma y color:SolidPeso molecular:332.31Saframycin Mx2
CAS:<p>Saframycin Mx2 exhibits activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C29H38N4O8Forma y color:SolidPeso molecular:570.6346-Hydroxytetrangulol
CAS:<p>6-Hydroxytetrangulol is an inducer of CPP32 protease found in Streptomyces.</p>Fórmula:C19H12O5Forma y color:SolidPeso molecular:320.30Fluopsin C
CAS:<p>Fluopsin C is a copper-containing antibiotic with potent activity against both Gram-positive and Gram-negative bacteria, as well as antitumor properties.</p>Fórmula:C4H8CuN2O2S2Forma y color:SolidPeso molecular:243.795Monamycin D1
CAS:<p>Monamycin D1 is a lipopeptide antibiotic with activity against Gram-positive bacteria.</p>Fórmula:C34H57N7O8Peso molecular:691.86Haliangicin C
CAS:<p>Haliangicin C exhibits antifungal activity against filamentous fungi and also acts on oomycetes, although it does not possess antibacterial properties.</p>Fórmula:C22H32O5Forma y color:SolidPeso molecular:376.49Polyoxin L
CAS:<p>Polyoxin L is a nucleoside-type antifungal antibiotic that is notably effective against rice sheath blight.</p>Fórmula:C16H23N5O12Peso molecular:477.38Amidinomycin
CAS:<p>Amidinomycin primarily acts against Gram-positive bacteria.</p>Fórmula:C9H18N4OPeso molecular:198.27Curromycin A
CAS:<p>Curromycin A exhibits antibacterial activity against Gram-positive bacteria such as Bacillus subtilis. Additionally, it can inhibit the replication of the human immunodeficiency virus (HIV) and suppresses the growth of mouse melanoma B16 and leukemia P388 cells.</p>Fórmula:C38H55N3O10Forma y color:SolidPeso molecular:713.857Norplicacetin
CAS:<p>Norplicacetin exhibits activity against Gram-positive bacteria and mycobacteria.</p>Fórmula:C24H33N5O7Peso molecular:503.55Nafarelin acetate hydrate
CAS:<p>Nafarelin: a GnRH agonist used to treat endometriosis, precocious puberty, and control IVF. Delivered as a nasal spray. Marketed as Synarel by Pfizer.</p>Fórmula:C66H83N17O13·xC2H4O2·xH2OForma y color:SolidPeso molecular:1400.563Chandrananimycin A
CAS:<p>Chandrananimycin A exhibits activity against Mucorales fungi and shows efficacy against tumor cell lines such as CCL HT29, MFXF 529L, and MACL McF-7.</p>Fórmula:C14H10N2O4Forma y color:SolidPeso molecular:270.24Melanoxazal
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:167.16Papyracon 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:266.29Lucilactaene
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:401.45Basidalin
CAS:<p>Basidalin exhibits properties that allow it to combat Gram-positive and Gram-negative bacteria, as well as inhibiting the proliferation of L-1210 leukemia cells in mice.</p>Fórmula:C6H5NO3Forma y color:SolidPeso molecular:139.109Octacosamicin A
CAS:<p>Octacosamicin A exhibits activity against bacteria, yeast, and filamentous fungi, although its antibacterial effects are relatively weak.</p>Fórmula:C31H52N4O9Forma y color:SolidPeso molecular:624.766Glaucarubin
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:496.55Bacithrocin A
CAS:<p>Bacithrocin C is a thrombin inhibitor that also suppresses factor Xa, trypsin, and papain, with IC50 values of 48 μM, 13 μM, 0.65 μM, and 0.02 μM, respectively.</p>Fórmula:C20H31N5O3Forma y color:SolidPeso molecular:389.492Quinocycline B
CAS:<p>Quinocycline B is a quinone and other glycoside antibiotic that demonstrates resistance to Gram-positive bacteria.</p>Fórmula:C33H32N2O10Forma y color:SolidPeso molecular:616.625,6-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:128.13Cepacin A
CAS:<p>Cepacin A is an alkyne antibiotic with antibacterial properties, exhibiting a minimum inhibitory concentration (MIC) of 0.2 μg/mL against Staphylococcus. Additionally, Cepacin A displays a degree of toxicity in mice, with an LD50 of 30 mg/kg when administered intraperitoneally.</p>Fórmula:C16H14O4Forma y color:SolidPeso molecular:270.28Formadicin C
CAS:<p>Formadicin C exhibits the strongest activity among all components against certain strains of Pseudomonas, Proteus, and Alcaligenes.</p>Fórmula:C24H26N4O10Peso molecular:530.48Oxythiamine diphosphate ammonium
<p>Oxythiamin diphosphate ammonium is a potent inhibitor of transketolase (TK).</p>Forma y color:SolidPAT-347
CAS:<p>PAT-347 is a potent inhibitor of Autotaxin, an enzyme linked to cell survival and diseases like cancer and fibrosis.</p>Fórmula:C28H21ClF2N2O3SForma y color:SolidPeso molecular:538.99AM-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:460.95Lactonamycin
CAS:<p>Lactonamycin exhibits significant activity against Gram-positive bacteria, including Staphylococcus, Streptococcus, Enterococcus, MRSA (MIC of 0.39-0.78 μg/mL), and VRE (MIC of 0.39-0.78 μg/mL). It also demonstrates inhibitory effects on various tumor cell lines such as L-1210, P388, S180, FS-3, Ehrlich, and B16-BL5 (IC50 of 0.06-3.3 μg/mL).</p>Fórmula:C28H27NO12Forma y color:SolidPeso molecular:569.513Hexacyclinol
CAS:<p>Hexacyclinol exhibits moderate activity against Gram-positive bacteria and can inhibit oxidant production in yeast polysaccharide-stimulated polymorphonuclear leukocytes (PMNL) at concentrations of 4–40 μg/mL. It suppresses the growth of L-930 and K562 cells with IC50 values of 1.4 μg/mL and 0.4 μg/mL, respectively, and has an IC50 of 10 μg/mL for HeLa cells. Additionally, Hexacyclinol shows antimalarial activity, with an IC50 of 2.4 μg/mL against Plasmodium falciparum.</p>Fórmula:C23H28O7Forma y color:SolidPeso molecular:416.46TP3011
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:474.51Antiviral agent 7
<p>Antiviral agent 7 is a peptide-based coating that kills viruses.</p>Fórmula:C29H31F2N3O6Forma y color:SolidPeso molecular:555.57Phenazostatin A
CAS:<p>Phenazostatin A is a phenazine compound 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. Phenazostatin A inhibits glutamate toxicity in N18-RE-105 cells with an EC50 of 0.34 μg/mL.</p>Fórmula:C28H20N4O3Forma y color:SolidPeso molecular:460.48Heme 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:339.82Defucogilvocarcin V
CAS:<p>Defucogilvocarcin V is an antibiotic with activity against Gram-positive bacteria.</p>Fórmula:C21H16O5Forma y color:SolidPeso molecular:348.349PD-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:488.37IACS-8779
CAS:<p>IACS-8779 is a potent STING agonist that efficiently stimulates interferon gene activity and exhibits strong systemic antitumor effects.</p>Fórmula:C21H25N9O10P2S2Pureza:98%Forma y color:SolidPeso molecular:689.55SIK1 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:404.50Irinotecan Carboxylate Sodium Salt
CAS:<p>Irinotecan Carboxylate Sodium Salt is a DNA topoisomerase inhibitor.</p>Fórmula:C33H39N4NaO7Forma y color:SolidPeso molecular:626.68Thiazolo[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:439.51Pulvilloric acid
CAS:<p>Pulvilloric acid is an antifungal antibiotic produced by the organism Pen. pulvillorum 504.</p>Fórmula:C15H18O5Forma y color:SolidPeso molecular:278.30Fandosentan
CAS:<p>Fandosentan is an endothelin receptor antagonist.</p>Fórmula:C25H18F3NO6SForma y color:SolidPeso molecular:517.475-Hydroxymethylblasticidin S
CAS:<p>5-Hydroxymethylblasticidin S is a broad-spectrum antibiotic found in Streptomyces setonii.</p>Fórmula:C18H28N8O6Forma y color:SolidPeso molecular:452.465ABL-001-Amide-PEG3-acid
ABL-001-Amide-PEG3-acid, an analogue to ABL-001, primarily serves as a labeled chemical or fluorescent probe.Fórmula:C29H33ClF2N6O9Pureza:98%Forma y color:SolidPeso molecular:683.0611-Hydroxynovobiocin
CAS:<p>11-Hydroxynovobiocin exhibits activity against Gram-negative bacteria.</p>Fórmula:C31H36N2O12Forma y color:SolidPeso molecular:628.62Chicamycin B
CAS:<p>Chicamycin B exhibits antitumor properties and has mild activity against gram-positive bacteria.</p>Fórmula:C13H14N2O4Forma y color:SolidPeso molecular:262.261Fulvoferruginin
CAS:<p>Fulvoferruginin exhibits cytotoxicity and antifungal properties, particularly against Paecilomyces.</p>Fórmula:C15H18O3Forma y color:SolidPeso molecular:246.30Lividomycin B
CAS:<p>Lividomycin B is an aminoglycoside antibiotic with broad-spectrum activity against bacteria and mycobacteria. It does not exhibit cross-resistance with Streptomyces or Penicillium. Additionally, it offers protective effects in mice infected with Staphylococcus aureus and Pseudomonas aeruginosa.</p>Fórmula:C23H45N5O13Forma y color:SolidPeso molecular:599.629Griseorhodin C
CAS:<p>Griseorhodin C is a quinone antibiotic primarily active against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C25H18O13Forma y color:SolidPeso molecular:526.40Octacosamicin B
CAS:<p>Octacosamicin B exhibits activity against bacteria, yeast, and filamentous fungi, although its antibacterial effectiveness is relatively weak.</p>Fórmula:C32H54N4O9Forma y color:SolidPeso molecular:638.793RDN2150
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:577.03DG013A
CAS:<p>DG013A inhibits ERAP1 & ERAP2 (IC50: 33 nM & 11 nM) to research autoimmune diseases & cancer.</p>Fórmula:C27H37N4O4PForma y color:SolidPeso molecular:512.58CI 922
CAS:<p>CI 922 is an anaphylaxis mediator release inhibitor. It inhibits the activation of human neutrophils.</p>Fórmula:C26H30N10O6Forma y color:SolidPeso molecular:578.58Antitrypanosomal agent 6
<p>Compound 18a: potent vs. T. brucei (IC50: 0.47 μM), >2x efficacy compared to Nifurtimox, good ADME, binds AT-rich DNA.</p>Fórmula:C22H29Cl2N5OForma y color:SolidPeso molecular:450.4Pluracidomycin D
CAS:<p>Pluracidomycin D, a type of carbapenem antibiotic, exhibits activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C9H11NO7SForma y color:SolidPeso molecular:277.252,3-Dimethoxy-4-(methylthio)benzeneethanamine
CAS:<p>2,3-Dimethoxy-4-(methylthio)benzeneethanamine (compound 22) is an analog of methoxybenzothiazine, employed in researching pharmacological agents that model human psychiatric disorders.</p>Fórmula:C11H17NO2SForma y color:SolidPeso molecular:227.32Epithienamycin B
CAS:<p>Epithienamycin B is a natural product isolated from Streptomyces flavoviridis.</p>Fórmula:C13H16N2O5SForma y color:SolidPeso molecular:312.34Porphine
CAS:<p>Porphine (Porphyrin), the parent compound of the porphyrin family, plays a crucial role within biological systems.</p>Fórmula:C20H14N4Forma y color:SolidPeso molecular:310.355-Fluoroorotic acid monohydrate
CAS:<p>5-Fluoroorotic acid (monohydrate) (5-Fluorouracil-6-carboxylic acid Mono(hydrate); 5-FOA) is employed to detect the expression of the URA3 gene in yeast molecular genetic constructs. Yeast possessing an active URA3 gene (which encodes orotidine-5'-monophosphate decarboxylase) convert 5-FOA into 5-fluorodeoxyuridine, a substance toxic to cells. Yeast strains with mutations in the URA3 gene that confer resistance can grow in the presence of 5-FOA if uracil is added to the medium.</p>Fórmula:C5H5FN2O5Forma y color:SolidPeso molecular:192.10CHNQD-01255
CAS:<p>CHNQD-01255 is an orally active inhibitor of Arf-GEFs that is effective against hepatocellular carcinoma (HCC).</p>Fórmula:C23H29NO6Forma y color:SolidPeso molecular:415.48Terfluranol
CAS:<p>Terfluranol, a benzyl derivative, is utilized as an antitumor medication.</p>Fórmula:C17H17F3O2Forma y color:SolidPeso molecular:310.31Octahydrocyclopenta[c]pyrrole
CAS:<p>Octahydrocyclopenta[c]pyrrole has demonstrated promising applications in the fields of anti-inflammatory, anti-tumor, and neuroprotection. The unique structure-activity relationship of Octahydrocyclopenta[c]pyrrole offers fresh insights for the design of new drugs.</p>Fórmula:C7H13NForma y color:SolidPeso molecular:111.18DC41
CAS:<p>DC41 is a CC-1065-based cancer drug, an antibody-linked DNA alkylator.</p>Fórmula:C37H34ClN5O4SPureza:98%Forma y color:SolidPeso molecular:680.22FTI-2148
CAS:<p>FTI-2148 blocks RAS-related FT-1 & GGT-1; IC50: 1.4 nM & 1.7 μM.</p>Fórmula:C24H28N4O3SPureza:98%Forma y color:SolidPeso molecular:452.57Novokinin
CAS:<p>Angiotensin AT2 receptor agonist</p>Fórmula:C39H61N11O7Pureza:98%Forma y color:SolidPeso molecular:795.97Mifepristone 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:480.08
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