Outros inibidores
Esta categoria abrange uma ampla variedade de inibidores que não se encaixam nas classificações padrão, mas que ainda são essenciais para várias pesquisas bioquímicas e farmacológicas. Esses inibidores podem direcionar vias, enzimas e interações moleculares únicas ou menos estudadas, fornecendo ferramentas valiosas para áreas de pesquisa especializadas. Na CymitQuimica, oferecemos uma seleção diversificada de inibidores de alta qualidade que abrangem múltiplos alvos biológicos e disciplinas de pesquisa, permitindo que você explore novas vias terapêuticas e aprofunde sua compreensão de processos biológicos complexos.
Foram encontrados 36770 produtos de "Outros inibidores"
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Copper(II) ionophore I
CAS:Copper(II) ionophore I is an active compound.Fórmula:C26H44N2S4Cor e Forma:SolidPeso molecular:512.90AZD-3199 dihydrobromide
CAS:<p>AZD-3199 dihydrobromide is a β2 adrenergic receptor agonist potentially for the treatment of asthma and chronic obstructive.</p>Fórmula:C32H44Br2N4O4SCor e Forma:SolidPeso molecular:740.59SENP2-IN-1
CAS:SENP2-IN-1 selectively inhibits SENP2, SENP1, and SENP5 with low IC50 values; useful in cancer studies.Fórmula:C32H29N3O5S2Cor e Forma:SolidPeso molecular:599.72M-COPA
CAS:M-COPA disrupts Golgi, blocks MET & Arf1 activation, and inhibits angiogenesis via VEGFR & NF-kB pathways.Fórmula:C25H34N2O2Cor e Forma:SolidPeso molecular:394.55Oudenone
CAS:<p>Oudenone is an oxygen-containing heterocyclic antibiotic with mild antibacterial and antifungal properties. It also exhibits antihypertensive effects in rats with spontaneous hypertension.</p>Fórmula:C12H16O3Cor e Forma:SolidPeso molecular:208.254L-739750
CAS:<p>L-739,750 is an inhibitor (FTI) of peptidomimetic farnesyltransferase.</p>Fórmula:C23H39N3O6S2Pureza:98%Cor e Forma:SolidPeso molecular:517.7PARP10/15-IN-1
PARP10/15-IN-1 (compound 8l) is a dual PARP10 and PARP15 inhibitor with IC50s of 160 nM and 370 nM, respectively. It can be used in cancer research[1].Fórmula:C13H10N2O3SCor e Forma:SolidPeso molecular:274.3Ataprost
CAS:Ataprost (ONO 41483), an oral Carboprostacyclin analogue, is 2.6x more potent in inhibiting ADP-induced platelet aggregation and can relieve coronary spasm.Fórmula:C21H32O4Cor e Forma:SolidPeso molecular:348.48PDE4-IN-12
PDE4-IN-12 is a potent and safe PDE4 ubiquitous inhibitor that acts on PDE4 (IC50: 3.5 nM, SI: 2.71) and PDE7 (IC50: 15 nM, SI: 4.27).Fórmula:C34H35NO6Cor e Forma:SolidPeso molecular:553.64BRD-K25923209
CAS:BRD-K25923209 is a novel inhibitor of BAF transcriptional repression.Fórmula:C29H36N4O3Cor e Forma:SolidPeso molecular:488.62MSK-195
CAS:MSK-195 is an effective TRPV1 agonist.Fórmula:C28H40N2O5Pureza:98%Cor e Forma:SolidPeso molecular:484.63Miyakamide B2
CAS:Miyakamide B2 is an antibiotic with insecticidal properties. It suppresses the growth of brine shrimp and shows weak activity against Xanthomonas species. The IC50 for inhibition of P388 cells by Miyakamide B2 is 7.6 μg/mL.Fórmula:C31H32N4O4Cor e Forma:SolidPeso molecular:524.612-PPA
CAS:2-PPA serves as a selective TMEM175 inhibitor (IC 50 =32 μM), primarily influencing lysosomal activity. Through acute inhibition of TMEM175, 2-PPA enhances lysosomal macromolecular catabolism, which in turn boosts macrophage activity and other digestive processes. This compound holds significance in Parkinson's disease research.Fórmula:C11H10N2Cor e Forma:SolidPeso molecular:170.21Fumarranol
CAS:Fumarranol inhibits angiogenesis and malaria growth by targeting PfMAP2.Fórmula:C16H24O4Cor e Forma:SolidPeso molecular:280.36Longicoricin
CAS:<p>Longicoricin is a monotetrahydrofuran Annonaceous acetogenin from Asimina longifolia.</p>Fórmula:C37H68O6Cor e Forma:SolidPeso molecular:608.93MRS-2339
CAS:MRS-2339 is a P2X receptor activator.Fórmula:C12H15ClN5O6PCor e Forma:SolidPeso molecular:391.70Vimirogant hydrochloride
Vimirogant (VTP-43742) HCl: Oral, selective RORγt inhibitor (IC50: 17 nM, Ki: 3.5 nM), >1000x selectivity over RORα/β, targets Th17, not Th1/2/Treg.Fórmula:C27H36ClF3N4O3SCor e Forma:SolidPeso molecular:588.21487UTPγS trisodium salt
CAS:P2Y2 and P2Y4 receptor agonistFórmula:C9H12N2Na3O14P3SPureza:98%Cor e Forma:SolidPeso molecular:566.15CN-716 HCl
CAS:cn-716 is a novel Zika virus (ZIKV) NS2B-NS3pro protease inhibitor.Fórmula:C22H33BCl2N6O4Cor e Forma:SolidPeso molecular:527.25Croconic acid disodium
CAS:<p>Croconic acid (disodium) (Nacr) enhances gene expression related to lysine crotonylation (Kcr) modification, which promotes cell growth and proliferation. This compound also shows promise in boosting somatic cell nuclear transfer (SCNT) efficiency and optimizing research in cell culture conditions.</p>Fórmula:C5Na2O5Cor e Forma:SolidPeso molecular:186.03SGLT1/2-IN-1
CAS:SGLT1/2-IN-1 is a dual SGLT1/SGLT2 inhibitor.Fórmula:C25H28O8Cor e Forma:SolidPeso molecular:456.48NRMA-8
CAS:<p>NRMA-8 is a small-molecule nuclear receptor modulator capable of penetrating the brain. It holds potential for research into central nervous system (CNS) diseases, including Alzheimer's disease, Parkinson's disease, demyelinating diseases, and glioblastoma.</p>Fórmula:C20H23ClN2O3Cor e Forma:SolidPeso molecular:374.86AP-6
CAS:AP-6, a selective TMEM175 inhibitor, enhances lysosomal macromolecular catabolism by acutely inhibiting TMEM175, thus speeding up macrophage and other digestive activities. This compound holds potential for use in Parkinson's disease research due to its role in modulating lysosomal function.Fórmula:C16H14N4Cor e Forma:SolidPeso molecular:262.31OP-2507
CAS:OP-2507, a prostacyclin agonist, is used potentially for the treatment of hepatic insufficiency and hypertension.Fórmula:C25H41NO4Pureza:98%Cor e Forma:SolidPeso molecular:419.6CH-38083
CAS:CH-38083 is a selective and effective alpha-2 adrenoceptors antagonist.Fórmula:C18H24ClNO3Pureza:98%Cor e Forma:SolidPeso molecular:337.84GS-9160
CAS: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.Fórmula:C20H18FN3O4SCor e Forma:SolidPeso molecular:415.44AM-3189
CAS:<p>AM-3189: potent, selective GPR40 agonist with low CNS penetration, good pharmacokinetics, and efficacy mirroring AMG 837.</p>Fórmula:C27H25ClN2O3Cor e Forma:SolidPeso molecular:460.95NS2B/NS3-IN-4
CAS:<p>Compound 34e inhibits DENV2/ZIKV proteases; IC50: 0.69 µM (DENV2), 1.04 µM (ZIKV).</p>Fórmula:C15H11NO4Cor e Forma:SolidPeso molecular:269.25Butaprost
CAS:<p>Butaprost: EP2 receptor agonist, EC50=33 nM, Ki=2.4 μM (murine), reduces fibrosis via TGF-β/Smad2.</p>Fórmula:C24H40O5Pureza:98%Cor e Forma:SolidPeso molecular:408.57AMG-222 tosylate
CAS:<p>AMG-222 tosylate is a DPP-IV inhibitor in clinical development for type II diabetes.</p>Fórmula:C39H47N9O6SCor e Forma:SolidPeso molecular:769.91DC1SMe
CAS:<p>DC1, a CC-1065-like ADC cytotoxin, is used in cancer-targeting antibody-drug conjugates. DC1Sme, a derivative, has IC50s: 22-250 pm in various cancer cells.</p>Fórmula:C35H30ClN5O4S2Pureza:98%Cor e Forma:SolidPeso molecular:684.23Fosfazinomycin B
CAS:<p>Fosfazinomycin B exhibits activity against plant pathogenic fungi such as the rice blast pathogen (Xanthomonas oryzae).</p>Fórmula:C10H23N6O6PCor e Forma:SolidPeso molecular:354.3GW-597901 cinnamate
CAS:<p>GW-597901 cinnamate is a long-acting beta(2)-agonist.</p>Fórmula:C34H46N2O8SCor e Forma:SolidPeso molecular:642.80RORγt inhibitor 2
CAS:<p>RORγt Inhibitor 2, a potent inhibitor of RORγt, exhibits an IC50 of 9.2 nM and is utilized in the study of cancer, inflammation, or autoimmune diseases that are</p>Fórmula:C31H33F5N2O7SCor e Forma:SolidPeso molecular:672.66P-gp modulator 3
<p>P-gp modulator 3 (Compound 37) is a potent, competitive, metabotropic P-glycoprotein (P-gp) modulator.</p>Fórmula:C31H37N3O5Cor e Forma:SolidPeso molecular:531.643HKT-IN-1
CAS:3HKT-IN-1 (Compound 17122279) is an inhibitor of Anopheles gambiae 3-hydroxykynurenine transaminase (3HKT) and is utilized in malaria research.Fórmula:C12H11BrN2O3Cor e Forma:SolidPeso molecular:311.131Antitumor agent-75
<p>Antitumor agent-75 is a novel and potent antitumor agent.</p>Fórmula:C26H23FN6Cor e Forma:SolidPeso molecular:438.5Haliangicin D
CAS:<p>Haliangicin D exhibits antifungal activity against filamentous fungi and is also effective against oomycetes, though it lacks antibacterial properties.</p>Fórmula:C22H32O5Cor e Forma:SolidPeso molecular:376.49MK-1220
CAS:MK-1220 is a novel Macrocyclic Inhibitor of Hepatitis C Virus NS3/4A Protease with Improved Preclinical Plasma Exposure.Fórmula:C40H53N5O9SCor e Forma:SolidPeso molecular:779.94SL agonist 1
CAS:<p>SL agonist 1, a Strigolactone (SL) agonist, is effective in promoting Arabidopsis seed germination through its recognition by the SL receptors OmKAI2d3 and OmKAI2d4.</p>Fórmula:C11H8FNO5Cor e Forma:SolidPeso molecular:253.18SARS-CoV-2 nsp14-IN-2
<p>SARS-CoV-2 nsp14-IN-2: Strong Nsp14 methyltransferase inhibitor (IC50: 0.09 μM), potential for COVID-19 research.</p>Fórmula:C21H21N5O5SCor e Forma:SolidPeso molecular:455.49KT2-962
CAS:<p>KT2-962 is a TXA2/prostaglandin endoperoxide receptor antagonist.</p>Fórmula:C23H27ClNNaO5S2Cor e Forma:SolidPeso molecular:520.04Memnobotrin B
CAS:Memnobotrin B is an antibiotic that exhibits inhibitory effects on the NCI-460, MCF7, and SF-268 cell lines.Fórmula:C27H37NO6Cor e Forma:SolidPeso molecular:471.59Topoisomerase I/II inhibitor 2
<p>Compound 1a inhibits Topoisomerase I/II, shrinks mouse liver tumors, IC50: 6.83/9.82 μM for LM9/Huh7 cells.</p>Fórmula:C19H16N2O4Cor e Forma:SolidPeso molecular:336.34Coriolin B
CAS:<p>Coriolin B exhibits activity against Gram-positive bacteria, weak activity against Gram-negative bacteria, yeast, and Trichomonas vaginalis. At a concentration of 5 μg/mL, Coriolin B inhibits 61.6% of Yoshida sarcoma growth but shows no inhibitory effect on Ehrlich ascites carcinoma in animals.</p>Fórmula:C23H36O6Cor e Forma:SolidPeso molecular:408.528Diarylalkane derivative 1
CAS:Diarylalkane derivative 1 is used for the research of pancreatitis.Fórmula:C34H51NO4Pureza:98%Cor e Forma:SolidPeso molecular:537.77Epicochlioquinone A
CAS:<p>Epicochlioquinone A inhibits rat liver microsomal ACAT with an IC50 of 1.7 μM and inhibits plasma lecithin-cholesterol acyltransferase (LCAT) with an IC50 of 15.8 μM. At a dosage of 75 mg/kg, it can reduce cholesterol absorption in rats by 50%.</p>Fórmula:C30H44O8Cor e Forma:SolidPeso molecular:532.666ASB14780
ASB14780 is a 4-phenoxy derivative and an inhibitor of cytoplasmic phospholipase cPLA2α (IC50: 20 nM).Cor e Forma:SolidCarmegliptin dihydrochloride
CAS:<p>Carmegliptin dihydrochloride (RG-1579, RO4876904) is a salt of Camegliptin, a DPP-4 inhibitor for type 2 diabetes.</p>Fórmula:C20H30Cl2FN3O3Cor e Forma:SolidPeso molecular:450.38Heme 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:C19H18ClN3OCor e Forma:SolidPeso molecular:339.82SK&F 108361
CAS:<p>SK&F 108361 is a symmetric diol that binds HIV-1 protease symmetrically.</p>Fórmula:C24H48N6O6Cor e Forma:SolidPeso molecular:516.67EP-7041 HCl
CAS:EP-7041 is a novel, potent, and selective Factor XIa inhibitor.Fórmula:C19H27ClN4O4Cor e Forma:SolidPeso molecular:410.89STA-1474
CAS:STA-1474, a soluble prodrug of ganetespib (STA-9090), becomes a strong HSP90 inhibitor effective against canine tumors.Fórmula:C20H21N4O6PCor e Forma:SolidPeso molecular:444.38PTP1B-IN-18
PTP1B-IN-18 is an orally active, fully mixed protein tyrosine phosphatase 1B (PTP1B) inhibitor (Ki: 35.2 μM).PTP1B-IN-18 can be used to study type 2 diabetes.Fórmula:C26H19N3O4SCor e Forma:SolidPeso molecular:469.51CU-2010
CAS:<p>CU-2010 is a synthetic compound that reduces blood loss and aids recovery post-cardiac surgery.</p>Fórmula:C37H42N6O6SCor e Forma:SolidPeso molecular:698.83L-2,5-Dihydrophenylalanine
CAS:<p>L-2,5-Dihydrophenylalanine can induce apoptosis in human medulloblastoma leukemia cells [HL-60].</p>Fórmula:C9H13NO2Cor e Forma:SolidPeso molecular:167.2113-Hydroxyglucopiericidin A
CAS:13-Hydroxyglucopiericidin A is an antibiotic with potent antitumor cell activity.Fórmula:C31H47NO10Cor e Forma:SolidPeso molecular:593.706Pradimicin Q
CAS:Pradimicin Q is an antibiotic exhibiting cytotoxicity against human colon HCT-116 cells and mouse melanoma B16-F10 cells, with IC50 values of 75 μg/mL and 100 μg/mL, respectively.Fórmula:C24H16O10Cor e Forma:SolidPeso molecular:464.378PD-L1-IN-1
<p>PD-L1-IN-1, potent PD-L1 inhibitor with 115 nM IC50, suppresses tumors, boosts immune response, and spares healthy cells.</p>Fórmula:C21H23N5O2Cor e Forma:SolidPeso molecular:377.44Pulvilloric acid
CAS:Pulvilloric acid is an antifungal antibiotic produced by the organism Pen. pulvillorum 504.Fórmula:C15H18O5Cor e Forma:SolidPeso molecular:278.30LAF-153
CAS:LAF-153 is a reversible Methionine Aminopeptidase‑2 (MetAP-2) Inhibitor.Fórmula:C18H32N2O7Cor e Forma:SolidPeso molecular:388.46KUS121
CAS:<p>KUS121: VCP ATPase activity inhibitor (IC50=330 nM), protects cells from ER stress, assists in cerebral ischemia, and preserves vision in retinitis pigmentosa.</p>Fórmula:C22H17FN4NaO3SCor e Forma:SolidPeso molecular:459.45PKG1α activator 3
PKG1α activator 3 is a PKG1α activator (EC50basal/partial=13/0.52 μM).Fórmula:C27H26Cl2N2O6Cor e Forma:SolidPeso molecular:545.41LY2934747
CAS:<p>LY2934747 is a novel, potent, and systemically bioavailable mGlu2/3 receptor agonist, exhibiting both antipsychotic and analgesic properties in vivo.</p>Fórmula:C10H13NO4Cor e Forma:SolidPeso molecular:211.21IACS-8779 disodium
CAS:IACS-8779 disodium: potent STING agonist, strong systemic anti-tumor effects, effective in melanoma model.Fórmula:C21H23N9Na2O10P2S2Cor e Forma:SolidPeso molecular:733.52Defucogilvocarcin V
CAS:<p>Defucogilvocarcin V is an antibiotic with activity against Gram-positive bacteria.</p>Fórmula:C21H16O5Cor e Forma:SolidPeso molecular:348.349Phenazostatin 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:C28H20N4O3Cor e Forma:SolidPeso molecular:460.48Curromycin 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:C38H55N3O10Cor e Forma:SolidPeso molecular:713.857Bacithrocin C
CAS:Bacithrocin C is a thrombin inhibitor that suppresses the activity of thrombin, factor Xa, trypsin, and papain, with IC50 values of 80 μM, 15 μM, 1.3 μM, and 0.02 μM, respectively.Fórmula:C18H27N5O3Cor e Forma:SolidPeso molecular:361.439Dienomycin B
CAS:<p>Dienomycin B exhibits mild antibacterial activity.</p>Fórmula:C18H23NO2Cor e Forma:SolidPeso molecular:285.38Barixibat
CAS:Barixibat is a bile acid transport inhibitor.Fórmula:C42H55N5O8Cor e Forma:SolidPeso molecular:757.91Fusarin C
CAS:Fusarin C is a mutagenic compound found in strains of the Fusarium genus.Fórmula:C23H29NO7Cor e Forma:SolidPeso molecular:431.479Exfoliamycin
CAS:<p>Exfoliamycin is a naphthoquinone antibiotic found in the Streptomyces strain Exfoliamycin Tu 1424, and it exhibits activity against Gram-positive bacteria.</p>Fórmula:C22H26O9Cor e Forma:SolidPeso molecular:434.436Vulolisib
CAS:<p>Vulolisib inhibits PI3K (α: IC50 0.2nM, β: 168nM, γ: 90nM, δ: 49nM), taken orally with anti-cancer properties.</p>Fórmula:C18H19F2N5O3SCor e Forma:SolidPeso molecular:423.44Antibiotic 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:C42H55NO16Cor e Forma:SolidPeso molecular:829.88Fudecalone
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:C15H22O3Cor e Forma:SolidPeso molecular:250.33Oximidine Ⅲ
CAS:<p>Oximidine III is an antitumor antibiotic that selectively inhibits the growth of rat fibroblast 3Y1 cells and induces mutations in various tumor genes. The inhibitory effects of Oximidine III on vH-ras-3Y1, v-src-3Y1 cells, and normal 3Y1 cells have IC50 values of 14 nM, 4.5 nM, and 140 nM, respectively. Additionally, Oximidine III arrests cells with RAS or SRC mutations in the G1 phase of the cell cycle and increases the expression of p21WAF1.</p>Fórmula:C23H24N2O6Cor e Forma:SolidPeso molecular:424.45Cremeomycin
CAS:<p>Cremeomycin exhibits activity against Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA), with a minimum inhibitory concentration (MIC) of 0.2-0.39 μg/mL. It also demonstrates cytotoxic effects in vitro against mouse tumor cell lines P388, L1210, IMC, S180, B16, and SS3.</p>Fórmula:C8H6N2O4Cor e Forma:SolidPeso molecular:194.144RORγt modulator 5
CAS:<p>RORγt modulator 5, a potent RORγt modulator, exhibits a dissociation constant (K_i) of <100 nM.</p>Fórmula:C27H22F5N3O6SCor e Forma:SolidPeso molecular:611.549-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:C20H30O2Cor e Forma:SolidPeso molecular:302.451AZD-4121
CAS:<p>AZD-4121 is an oral cholesterol absorption inhibitor targeting NPC1L1 for the treatment of dyslipidaemia.</p>Fórmula:C36H39F2N3O7SCor e Forma:SolidPeso molecular:695.77Anticancer 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:C20H12F3NO5Cor e Forma:SolidPeso molecular:403.31Terfluranol
CAS:Terfluranol, a benzyl derivative, is utilized as an antitumor medication.Fórmula:C17H17F3O2Cor e Forma:SolidPeso molecular:310.31Rivenprost
CAS:Rivenprost, selective EP4 agonist (Ki: 0.7 nM), promotes bone growth, osteoblast differentiation, and aids wound healing.Fórmula:C24H34O6SCor e Forma:SolidPeso molecular:450.59Glidobactin 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:C27H44N4O7Cor e Forma:SolidPeso molecular:536.6613-O-Demethylmonensin A
CAS:3-O-Demethylmonensin A is a polyether antibiotic produced by Streptomyces cinnamonensis (strain LO-63).Fórmula:C35H60O11Cor e Forma:SolidPeso molecular:656.84Seldomycin factor 1
CAS:Seldomycin factor 1 (XK 88-1) is an aminoglycoside antibiotic known for its broad-spectrum antibacterial activity.Fórmula:C17H34N4O10Cor e Forma:SolidPeso molecular:454.473Gentamicin C2
CAS:<p>Gentamicin C2 is an aminoglycoside antibiotic.</p>Fórmula:C20H41N5O7Cor e Forma:SolidPeso molecular:463.569Lunacalcipol
CAS:Lunacalcipol is used for the treatment of Secondary Hyperparathyroidism.Fórmula:C28H42O4SCor e Forma:SolidPeso molecular:474.79(S),10(S),13(S)-TriHOME
CAS:9(S),10(S),13(S)-TriHOME is an oxylipin derived from linoleic acid. It has been detected in beer and in bronchoalveolar lavage fluid (BALF) from female smokers.Fórmula:C18H34O5Cor e Forma:SolidPeso molecular:330.46Deoxyradicinin
CAS:<p>Deoxyradicinin is a biosynthetic precursor of Radicinin. It can inhibit Xylella fastidiosa and Liberibacter crescens, with a minimum inhibitory concentration (MIC) of 3.5 μg/mL against Liberibacter crescens. Deoxyradicinin is applicable for research on controlling plant diseases caused by these pathogens.</p>Fórmula:C12H12O4Cor e Forma:SolidPeso molecular:220.2211-Hydroxyoxaunomycin
CAS:<p>1-Hydroxyoxaunomycin is an antibiotic that inhibits the growth of U210 cells as well as the synthesis of DNA and RNA, with IC50 values of 0.0005 μg/mL, 1.00 μg/mL, and 0.76 μg/mL, respectively.</p>Fórmula:C26H29NO11Cor e Forma:SolidPeso molecular:531.50916-Hydroxyroridin L-2
CAS:<p>16-Hydroxyroridin L-2 is a member of the verrucarin subclass of antibiotics with antitumor properties.</p>Fórmula:C29H38O10Cor e Forma:SolidPeso molecular:546.606Antiviral agent 6
<p>Antiviral agent 6 showed excellent anti-TSWV effects in vivo (EC50: 188 mg/L).</p>Fórmula:C23H27BrN2O3S2Cor e Forma:SolidPeso molecular:523.51Avorelin acetate
CAS:<p>Avorelin acetate is a luteinizing hormone releasing hormone (LH-RH) agonist.</p>Fórmula:C67H89N17O14Cor e Forma:SolidPeso molecular:1356.55A 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%Cor e Forma:SolidPeso molecular:787.08Chrymutasin C
CAS:Chrymutasin C is a glycoside antitumor antibiotic with cytotoxic properties.Fórmula:C39H43NO17Cor e Forma:SolidPeso molecular:797.7554"-Demethylgentamicin C1
CAS:<p>4"-Demethylgentamicin C1 exhibits antibacterial activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C20H41N5O7Cor e Forma:SolidPeso molecular:463.57Nevirapine dimer
CAS:Nevirapine dimer is a non-nucleoside reverse transcriptase inhibitor (NNRTI).Fórmula:C30H26N8O2Cor e Forma:SolidPeso molecular:530.58NPEC-caged-(S)-3,4-DCPG
CAS:mGlu8a agonistFórmula:C19H16N2O10Pureza:98%Cor e Forma:SolidPeso molecular:432.34AS1940477
CAS:<p>AS1940477 selectively inhibits p38 MAPK α/β, blocks proinflammatory cytokines in cells, and has anti-inflammatory effects in rats.</p>Fórmula:C24H22FN5O2Cor e Forma:SolidPeso molecular:431.46RS 2135
CAS:RS 2135 is a novel class I antiarrhythmic agent to inhibit ischemia-induced ventricular arrhythmias.Fórmula:C18H21ClN2O2Pureza:98%Cor e Forma:SolidPeso molecular:332.83NTPDase-IN-2
CAS:<p>NTPDase-IN-2 inhibits h-NTPDase-2/-8 (IC50: 0.04, 2.27 µM), non-competitive for h-NTPDase-1/-2 (Km: 74 µM); useful in cancer, immune, bacterial research.</p>Fórmula:C24H20FN3OS2Cor e Forma:SolidPeso molecular:449.56G12Si-1
G12Si-1 selectively binds and inhibits K-Ras(G12S) to block oncogenic signaling and nucleotide exchange.Fórmula:C29H32ClN5O3Cor e Forma:SolidPeso molecular:534.05AVE-1330A free acid
CAS:AVE-1330A free acid is a broad-spectrum non-beta-lactam beta-lactamase inhibitor.Fórmula:C7H11N3O6SCor e Forma:SolidPeso molecular:265.2422-HDHA
CAS:22-HDHA is an oxidation product of docosahexaenoic acid .Fórmula:C22H32O3Cor e Forma:SolidPeso molecular:344.49BAY-693
CAS:<p>BAY-693 is a ERK5 negative control agent with IC50 (ERK5) = 6400 nM. Its analog, BAY-885, is a potent and selective ERK5 (MAPK7) inhibitor with IC50 of 40 nM</p>Fórmula:C26H30F3N7O2Cor e Forma:SolidPeso molecular:529.56SSM3 TFA
CAS:SSM3 TFA is a potent furin inhibitor, blocking furin-dependent cell surface processing of anthrax protective antigen-83 in vitro..Fórmula:C22H32N12O2Cor e Forma:SolidPeso molecular:496.57B-3852
CAS:B-3852 is a Bradykinin inhibitor.Fórmula:C55H74F3N15O11Cor e Forma:SolidPeso molecular:1178.27BAY-091
CAS:BAY-091 is a novel potent and highly selective PIP4K2A kinase inhibitor.Fórmula:C26H21FN4O2Pureza:97.66% - 99.23%Cor e Forma:SoildPeso molecular:440.47SGK1-IN-3
SGK1-IN-3: Potent oral inhibitor of SGK1, may target osteoarthritis.Fórmula:C23H20Cl2N6O3SCor e Forma:SolidPeso molecular:531.41UAWJ9-36-1
CAS:UAWJ9-36-1: potent broad-spectrum coronavirus Protease inhibitor; IC50 = 51 nM.Fórmula:C23H29N3O5Cor e Forma:SolidPeso molecular:427.49STA 2
CAS:STA 2 is an analogue of TXA2, a thromboxane receptor in the colonic epithelium.Fórmula:C21H34O3SCor e Forma:SolidPeso molecular:366.56Sannamycin J
CAS:Sannamycin J is an aminoglycoside antibiotic found in *Streptomyces sannanensis* sp. KC-7038. This compound exhibits relatively weak antibacterial activity against both Gram-positive and Gram-negative bacteria.Fórmula:C14H30N4O4Cor e Forma:SolidPeso molecular:318.41J-104132
CAS: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.Fórmula:C31H33NO7Pureza:98%Cor e Forma:SolidPeso molecular:531.60BMS-748730
CAS:<p>BMS-748730, also known as 4′-Hydroxy Dasatinib, is a Dasatinib metabolite.</p>Fórmula:C22H26ClN7O3SCor e Forma:SolidPeso molecular:504.01Homopteroic Acid
CAS:Homopteroic Acid, a precursor to Homofolic Acid, inhibits L1210 mouse leukemia growth by targeting folate uptake.Fórmula:C15H14N6O3Cor e Forma:SolidPeso molecular:326.31SIK1 activator 1
CAS:SIK1 activator 1 boosts SIK1 phosphorylation, reduces type 2 diabetes hyperglycemia, and inhibits liver gluconeogenesis.Fórmula:C23H32O6Cor e Forma:SolidPeso molecular:404.50(R)-ONO-2952
(R)-ONO-2952 is the R-enantiomer of ONO-2952. ONO-2952 is selective and oral effective TSPO antagonist, with Kis of 0.330-9.30 nM inhibiting rat and human TSPO.Fórmula:C22H20ClFN2O2Cor e Forma:SolidPeso molecular:398.86BILA 1906 BS
CAS:BILA 1906 BS is an inhibitor of substrate analog protease.Fórmula:C41H52N6O4SPureza:98%Cor e Forma:SolidPeso molecular:724.95Antimalarial agent 9
<p>Antimalarial 9, a quinoline-imidazole derivative, effectively targets CQ-susceptible (IC50-0.14 μM) and MDR strains (IC50-0.41 μM) with low toxicity.</p>Fórmula:C28H32BrN3O2Cor e Forma:SolidPeso molecular:522.48Mutatochrome
CAS:<p>Mutatochrome (Citroxanthin) is a compound found in plants.</p>Fórmula:C40H56OCor e Forma:SolidPeso molecular:552.872Plasma kallikrein-IN-2
Plasma kallikrein-IN-2: PKal inhibitor, IC50=0.1 nM. Used in angioedema, diabetic eye disease research.Fórmula:C28H24ClF3N8O3Cor e Forma:SolidPeso molecular:612.99FTO-IN-6
CAS:FTO-IN-6 is a selective inhibitor of fat mass and obesity associated protein (FTO).Fórmula:C14H12N4O6Cor e Forma:SolidPeso molecular:332.27GG-43
GG-43 is a potent inhibitor of LIN28. The IC50 value of GG-43 against human LIN28A is 4 μM [1].Fórmula:C21H21NO3Cor e Forma:SolidPeso molecular:335.4Olanzapine/Samidorphan
CAS:Olanzapine/Samidorphan, a tablet blending olanzapine and samidorphan, targets schizophrenia and bipolar I, curbing weight gain.Fórmula:C38H46N6O4SCor e Forma:SolidPeso molecular:682.88Parimycin
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:C22H20O7Cor e Forma:SolidPeso molecular:396.39ATX inhibitor 12
<p>Oral ATX inhibitor 12 (IC50: 1.72 nM) at 60 mg/kg prevents lung damage in C57Bl/6J mice.</p>Fórmula:C30H34FN5O2Cor e Forma:SolidPeso molecular:515.62Pacidamycin 5T
CAS:<p>Pacidamycin 5T is found in the bacterium Streptomyces coeruleorubidus [NRRL 18370].</p>Fórmula:C36H44N8O12Cor e Forma:SolidPeso molecular:780.78Nonsteroidal aromatase inhibitor 1
Compound 13h, a nonsteroidal aromatase inhibitor, has a potent IC50 of 0.09 nM against CYP19A1, showing promise for breast cancer research.Fórmula:C22H16N4O2Cor e Forma:SolidPeso molecular:368.39Pilatin
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:C21H26O7Cor e Forma:SolidPeso molecular:390.427AGN-204396
CAS:AGN-204396 is an antagonist that selectively blocks the activity of prostamides (prostaglandin-ethanolamides).Fórmula:C32H44FN3O4Cor e Forma:SolidPeso molecular:553.71PF-06815345 hydrochloride
CAS:<p>PF-06815345 HCl is an oral, potent PCSK9 inhibitor, IC50 13.4 μM, lowers PCSK9 in mice.</p>Fórmula:C27H30Cl2FN9O4Cor e Forma:SolidPeso molecular:634.49Pyrisulfoxin A
CAS:<p>Pyrisulfoxin A is an antibiotic that can be found in Streptomyces callfornicus [BS-75].</p>Fórmula:C13H13N3O3SCor e Forma:SolidPeso molecular:291.326Nnc 09-0026
CAS:Nnc 09-0026 is a neuronal calcium channel blockerFórmula:C25H35Cl2F3N2OCor e Forma:SolidPeso molecular:507.46GSK 932121
CAS:GSK 932121: potent antimalarial, targets P. falciparum by inhibiting cytochrome bc1 in the electron transport chain.Fórmula:C20H15ClF3NO4Pureza:98%Cor e Forma:SolidPeso molecular:425.79Dihydrocompactin
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:C23H36O5Cor e Forma:SolidPeso molecular:392.529CY208-243 Mandelate
CAS:CY208-243 is a D1 agonist boosting memory in T-maze, enhances adenylate cyclase (EC50=125nM), and alters monkey electroretinogram.Fórmula:C27H26N2O3Cor e Forma:SolidPeso molecular:426.52TAM&Met-IN-1
CAS:TAM&Met-IN-1 inhibits AXL, MER, TYRO3 with IC50s 6.1, 13.2, 21.6 nM, respectively, for cancer research.Fórmula:C29H27F2N7O5Cor e Forma:SolidPeso molecular:591.57AMG-315
CAS:AMG-315: Chiral AEA analogue, potent CB1 agonist (Ki 7.8 nM, EC50 0.6 nM), stable against hydrolyzing/oxidative enzymes.Fórmula:C24H41NO2Cor e Forma:SolidPeso molecular:375.59Roselipin 1A
CAS:<p>Roselipin 1A inhibits diacylglycerol acyltransferase (DGAT) in rats.</p>Fórmula:C40H72O14Cor e Forma:SolidPeso molecular:776.991EBI-907
CAS:EBI-907 is a potent, oral B-RafV600E inhibitor with an IC50 of 4.9 nM, over 10x stronger than Vemurafenib, and effective against key cancer kinases.Fórmula:C23H21ClF2N4O3SCor e Forma:SolidPeso molecular:506.95Antidepressant agent 2
<p>Antidepressant agent 2 showed significant antidepressant effects with a MED value of 0.1 mg/kg.</p>Fórmula:C21H22ClFN2O3SCor e Forma:SolidPeso molecular:436.93Artemisiane E
CAS:Artemisiane E is a potent PI3K/AKT pathway inhibitor with an IC 50 of 8.9 μM .Fórmula:C20H22O5Cor e Forma:SolidPeso molecular:342.39LY3325656
CAS:LY3325656, a GPR142 agonist with anti-diabetic properties, progresses to phase 1 trials for Type 2 diabetes.Fórmula:C21H23F3N6O2Cor e Forma:SolidPeso molecular:448.442-Hydroxybutirosin
CAS:2-Hydroxybutirosin is an antibiotic that can be found in Bacillus circulans.Fórmula:C21H41N5O13Cor e Forma:SolidPeso molecular:571.576Pradimicin B
CAS:Pradimicin B is an antibiotic with potent antifungal and anti-yeast activities.Fórmula:C35H36N2O14Cor e Forma:SolidPeso molecular:708.665Dephostatin
CAS:<p>Dephostatin is a competitive protein tyrosine phosphatase (PTP) inhibitor isolated from Streptomyces spp., exhibiting activity within the micromolar range.</p>Fórmula:C7H8N2O3Cor e Forma:SolidPeso molecular:168.15Cryptosporiopsin
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:C10H10Cl2O4Cor e Forma:SolidPeso molecular:265.099-Hydroxyoudemansin A
CAS:<p>9-Hydroxyoudemansin A exhibits antifungal activity with a minimum inhibitory concentration (MIC) of 12.5 μg/mL against Saccharomyces cerevisiae. It shows resistance to fungi such as Candida albicans, Rhodotorula, Penicillium, and Streptomyces, with MIC values all exceeding 50 μg/mL. It does not possess antibacterial properties.</p>Fórmula:C16H20O4Cor e Forma:SolidPeso molecular:276.32823-De(mycinosyloxy)tylosin
CAS:<p>23-De(mycinosyloxy)tylosin is a macrolide antibiotic exhibiting activity against Gram-positive bacteria, with limited efficacy against Gram-negative bacteria and mycoplasma.</p>Fórmula:C38H63NO12Cor e Forma:SolidPeso molecular:725.91UNC9426
CAS:<p>UNC9426 is an orally active, potent and selective TYRO3 inhibitor with an IC50 of 2.1 nM. UNC9426 reduces platelet aggregation without prolonging bleeding time.</p>Fórmula:C32H34F6N6OPureza:98.051%Cor e Forma:SolidPeso molecular:632.642Cuevaene A
CAS:<p>Cuevaene A can be isolated from the Streptomyces genus gdmAI-disrupted LZ35 strain. It exhibits moderate activity against Gram-positive bacteria, such as Bacillus subtilis (strain ATCC 11060), and demonstrates moderate activity against fungi, including Fusarium verticillioides (strain S68) and Rhizoctonia solani (strain GXE4).</p>Fórmula:C21H22O5Cor e Forma:SolidPeso molecular:354.396Anti-Trypanosoma cruzi agent-2
Compd 3b: anti-trypanosomal, IC50 0.51 μM (NINOA), 3.06 μM (INC-5), also combats T. gondii.Fórmula:C17H10ClNO5Cor e Forma:SolidPeso molecular:343.72Guanine-7-oxide
CAS: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.Fórmula:C5H5N5O2Cor e Forma:SolidPeso molecular:167.126SSTR5 antagonist 2 hydrochloride
SSTR5 antagonist 2 hydrochloride: potent, oral SSTR5 blocker with potential in type 2 diabetes research.Fórmula:C32H36ClFN2O5Cor e Forma:SolidPeso molecular:583.09FK-906 HCl
CAS:FK-906 HCl is a human renin inhibitor used for the long-term treatment of patients with essential hypertension.Fórmula:C40H64ClN7O7Cor e Forma:SolidPeso molecular:790.44NUCC-555
CAS: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.Fórmula:C25H25N5O3Pureza:98%Cor e Forma:SolidPeso molecular:443.5BSc5367
CAS:<p>BSc5367 inhibits Nek1 kinase (IC50: 11.5 nM), key in cell cycle, DNA repair, impacting ALS, PKD, cancer.</p>Fórmula:C20H15N3O2Cor e Forma:SoildPeso molecular:329.35Purine phosphoribosyltransferase-IN-1
Compound (S,R)-48 inhibits Pf, Pv, & Tbr PRT with Ki of 50, 20, 2 nM.Fórmula:C11H15N5Na4O10P2Cor e Forma:SolidPeso molecular:531.17Clecarmycin C
CAS:<p>Clecarmycin C is an antitumor antibiotic that demonstrates cytotoxic and antitumor properties. Additionally, Clecarmycin C exhibits antibacterial activity.</p>Fórmula:C29H26O11Cor e Forma:SolidPeso molecular:550.514-Diazo-3-methoxy-2,5-cyclohexadien-1-one
CAS:<p>4-Diazo-3-methoxy-2,5-cyclohexadien-1-one demonstrates notable activity against anaerobic bacteria. Minimum inhibitory concentrations (MIC) are 0.4 μg/mL for Clostridium and Bacteroidetes, and 0.2 μg/mL for Haemophilus.</p>Fórmula:C7H6N2O2Cor e Forma:SolidPeso molecular:150.14PAD-IN-2
CAS:<p>PAD-IN-2, potent PAD4 inhibitor, IC50 <1 μM; targets autoimmune/cancer disorders.</p>Fórmula:C27H28ClN5O2Cor e Forma:SolidPeso molecular:4902-Hydroxymethylclavam
CAS:<p>2-Hydroxymethylclavam is a β-lactam antibiotic with antifungal properties, particularly effective against plant pathogenic fungi.</p>Fórmula:C6H9NO3Cor e Forma:SolidPeso molecular:143.141Antitrypanosomal agent 5
Antitrypanosal agent 5 is a selective anti-trypanosomal agent that acts on T. brucei (IC50: 1 nM) and HEK293 cells (IC50: 483.3 μM).Fórmula:C30H30N6O4SCor e Forma:SolidPeso molecular:570.66Antimalarial agent 2
Antimalarial agent 2 is an orally active, novel antimalarial agent that exhibits rapid in vitro killing effects.Fórmula:C27H25N3O5Cor e Forma:SolidPeso molecular:471.5Juvenimicin A2
CAS:<p>Juvenimicin A2 is effective against Gram-positive bacteria and certain Gram-negative bacteria.</p>Fórmula:C30H51NO8Cor e Forma:SolidPeso molecular:553.7281-Deamino-1-hydroxygentamicin C1a
CAS:<p>1-Deamino-1-hydroxygentamicin C1a (AntibioticSU-2) is an aminoglycoside antibiotic effective against both gram-positive and gram-negative bacteria.</p>Fórmula:C19H38N4O8Cor e Forma:SolidPeso molecular:450.527VEGFR-2-IN-12
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.Fórmula:C22H24N6O3SCor e Forma:SolidPeso molecular:452.53Elaiomycin
CAS:Elaiomycin exhibits activity against Gram-positive bacteria, certain anaerobic bacteria, Eimeria tenella, and Eimeria stiedai.Fórmula:C13H26N2O3Cor e Forma:SolidPeso molecular:258.357Acetoxycycloheximide
CAS:<p>Acetoxycycloheximide triggers TNF receptor 1, prompts apoptosis, and cytochrome c release by activating c-Jun N-terminal kinase.</p>Fórmula:C17H25NO6Cor e Forma:SolidPeso molecular:339.38Deacetylravidomycin N-oxide
CAS:<p>Deacetylravidomycin N-oxide is an antibiotic produced by [Streptomyces ravidus S50905] that exhibits activity against Gram-positive bacteria but is inactive against Gram-negative bacteria. Additionally, Deacetylravidomycin N-oxide demonstrates antitumor properties against P388 leukemia and methylcholanthrene A fibrosarcoma.</p>Fórmula:C31H33NO10Cor e Forma:SolidPeso molecular:579.594FTO-IN-1 TFA
FTO-IN-1 TFA: FTO enzyme inhibitor, anti-obesity, IC50 < 1μM, potential cancer research tool.Fórmula:C20H17Cl2F3N4O4Cor e Forma:SolidPeso molecular:505.27ML-SI1
CAS:ML-SI1, a racemic mixture of diastereoisomers, is a TRPML inhibitor and acts on TRPML1 (IC50: 15 μM).Fórmula:C23H26Cl2N2O3Cor e Forma:SolidPeso molecular:449.37Lp-PLA2-IN-5
CAS:<p>Lp-PLA2-IN-5 inhibits Lp-PLA2 and PAF-AH, potentially useful in Alzheimer's and atherosclerosis studies.</p>Fórmula:C23H18F5N3O4Cor e Forma:SolidPeso molecular:495.4Reumycin
CAS:<p>Reumycin is a 7-azaindole antibiotic that exhibits cytotoxicity against tumor cells such as Ellrich carcinoma, Sarcoma-180, Sarcoma-37, and lymphosarcoma.</p>Fórmula:C6H5N5O2Cor e Forma:SolidPeso molecular:179.136Fumaryl-DL-alanine
CAS:Fumaryl-DL-alanine exhibits activity against Gram-positive bacteria.Fórmula:C7H9NO5Cor e Forma:SolidPeso molecular:187.1518:0-LPS
CAS: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.Fórmula:C24H48NO9PCor e Forma:SolidPeso molecular:525.613(25S)-δ7-Dafachronic acid
CAS:(25S)-delta7-Dafachronic acid, an orphan nuclear receptor DAF-12 ligand, inhibits the dauer-promoting activity of DAF-12.Fórmula:C27H42O3Pureza:98%Cor e Forma:SolidPeso molecular:414.62Haliangicin B
CAS:Haliangicin B exhibits activity against filamentous fungi and is also effective against oomycetes, but it does not possess any antibacterial properties.Fórmula:C22H32O5Cor e Forma:SolidPeso molecular:376.49Dihydroabikoviromycin
CAS:Dihydroabikoviromycin is a secondary metabolite of Streptomyces anulatus and acts as a polyketide synthase inhibitor.Fórmula:C10H13NOCor e Forma:SolidPeso molecular:163.216nNOS-IN-25
CAS:nNOS-IN-25 is an effective, selective, and cell-permeable inhibitor of neuronal nitric oxide synthase.Fórmula:C21H22N4Pureza:98%Cor e Forma:SolidPeso molecular:330.43AT-IAP
CAS:AT-IAP is an effective dual antagonist of XIAP and cIAP1.Fórmula:C29H40FN5O2Pureza:98%Cor e Forma:SolidPeso molecular:509.66Haliangicin A
CAS:<p>Haliangicin A exhibits antifungal activity against filamentous fungi and also affects oomycetes, though it does not possess antibacterial properties.</p>Fórmula:C22H32O5Cor e Forma:SolidPeso molecular:376.492-n-Heptyl-4-quinolinol
CAS:<p>2-n-Heptyl-4-quinolinol exhibits activity against Candida albicans, Staphylococcus aureus, Vibrio anguillarum, and Vibrio harveyi.</p>Fórmula:C16H21NOCor e Forma:SolidPeso molecular:243.34Pegcantratinib
CAS:Pegcantratinib is a tropomyosin receptor kinase inhibitor for treatment for inherited CYLD defective skin tumours.Fórmula:C32H28N4O7Cor e Forma:SolidPeso molecular:580.59Ici D1542
CAS:Ici D1542: potent TXS inhibitor & TXA2 receptor antagonist, effective thromboxane blocker in vitro.Fórmula:C25H30N2O7Pureza:98%Cor e Forma:SolidPeso molecular:470.51RIPK1-IN-24
CAS:<p>RIPK1-IN-24 is an inhibitor of receptor-interacting protein kinase 1 (RIPK1) with an IC50 of 1.3 μM. It is utilized in research on inflammatory diseases.</p>Fórmula:C26H21FN6O2Cor e Forma:SolidPeso molecular:468.48Coleon-U-quinone
CAS:Coleon-U-quinone, a P-gp inhibitor, reduces cancer cell viability and enhances Doxorubicin sensitivity in resistant cells.Fórmula:C20H24O5Cor e Forma:SolidPeso molecular:344.4Schidigera-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:C27H40O4Cor e Forma:SolidPeso molecular:428.6044"-Demethylgentamicin C2
CAS:4"-Demethylgentamicin C2 exhibits activity against both Gram-positive and Gram-negative bacteria.Fórmula:C19H39N5O7Cor e Forma:SolidPeso molecular:449.54Chitinovorin C
CAS:Chitinovorin C is a β-lactam class antibiotic (antibiotic) that exhibits weak inhibitory activity against Gram-negative bacteria.Fórmula:C15H20N4O8SCor e Forma:SolidPeso molecular:416.406Haloquinone
CAS:<p>Haloquinone is a quinone antibiotic that exhibits significant antibacterial activity against halophilic bacteria and is also effective against Gram-positive bacteria and mycoplasma.</p>Fórmula:C17H12O5Cor e Forma:SolidPeso molecular:296.274Epithienamycin C
CAS:<p>Epithienamycin C is a carbapenem antibiotic with activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C13H18N2O5SCor e Forma:SolidPeso molecular:314.357NCATS-SM4487
CAS:NCATS-SM4487 is a highly selective inhibitor of GALK1 (IC50: 0.05 μM).Fórmula:C25H24ClFN8O2Cor e Forma:SolidPeso molecular:522.96Ophiobolin D
CAS:Ophiobolin D is a terpene antibiotic with mild inhibitory effects on Staphylococcus aureus.Fórmula:C25H36O4Cor e Forma:SolidPeso molecular:400.55Pradimicin T2
CAS:<p>Pradimicin T2 is an antibiotic with activity against filamentous fungi and yeast-like fungi.</p>Fórmula:C37H37NO19Cor e Forma:SolidPeso molecular:799.685FW 34569
CAS:FW 34569, an enkephalin analog, boosts growth hormones and prolactin, reduces cortisol and LH; FSH stable.Fórmula:C30H43N5O7SPureza:98%Cor e Forma:SolidPeso molecular:617.76
