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 36533 produtos de "Outros inibidores"
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Cinatrin C2
CAS:<p>Cinatrin C2, a phospholipase A2 (PLA2) inhibitor, has an IC50 value of 800 μM and can be extracted from the Circinotrichum falcatisporum strain RF-641.</p>Fórmula:C18H30O8Cor e Forma:SolidPeso molecular:374.426Exicorilant
CAS:Exicorilant is a selective oral GR antagonist (Ki: 7 nM) that may reduce obesity, glucose intolerance, & dyslipidemia.Fórmula:C26H23F4N7O3SPureza:98%Cor e Forma:SolidPeso molecular:589.56Acetylstachyflin
CAS:Acetylstachyflin is an antibiotic effective against the influenza A virus.Fórmula:C25H33NO5Cor e Forma:SolidPeso molecular:427.53EP-7041 HCl
CAS:EP-7041 is a novel, potent, and selective Factor XIa inhibitor.Fórmula:C19H27ClN4O4Cor e Forma:SolidPeso molecular:410.89Cuevaene 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:354.396Niravoline
CAS:Niravoline is a kappa-opioid agonist.Fórmula:C22H25N3O3Cor e Forma:SolidPeso molecular:379.45Cenicriviroc Sulfone
CAS:Cenicriviroc Sulfone, a Cenicriviroc derivative, inhibits CCR2/CCR5 to block HIV entry into cells.Fórmula:C41H52N4O5SCor e Forma:SolidPeso molecular:712.94Melithiazole A
CAS:<p>Melithiazol A is an antibiotic and a potent β-methoxyacrylate (MOA) inhibitor with antifungal and cytotoxic properties.</p>Fórmula:C20H26N2O4S2Cor e Forma:SolidPeso molecular:422.561BM635 mesylate (1493762-74-5 free base)
BM635 mesylate is an MmpL3 inhibitor with outstanding anti-mycobacterial activity (MIC50: 0.12 μM against M. tuberculosis H37Rv).Fórmula:C26H33FN2O4SPureza:98%Cor e Forma:SolidPeso molecular:488.61Citrinin hydrate
CAS:Citrinin hydrate is an inhibitor of human rhinovirus (HRV) 3C protease, with an IC50 of 1.0 mM.Fórmula:C13H16O6Cor e Forma:SolidPeso molecular:268.263Antiallergic agent-1
Antiallergic agent-1, an Src family kinase inhibitor, is a new and valuable lead compound with potential as an anti-allergic agent.Fórmula:C27H19F6N5OCor e Forma:SolidPeso molecular:543.46Guanine-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:167.126eIF4A-IN-3
CAS:eIF4A-IN-3 (Compound 71E) is an inhibitor of the eukaryotic translation initiation factor 4A (eIF4A). This compound can be utilized as a cytotoxic payload for antibody-drug conjugates (ADCs).Fórmula:C34H37N3O7Cor e Forma:SolidPeso molecular:599.67Naphthablin
CAS:<p>Naphthablin is a naphthoquinone compound that inhibits the function of the Abl oncogene. It prevents the morphological transformation of v-ablts-NIH3T3 cells induced by Abl and also suppresses RNA synthesis.</p>Fórmula:C29H36O8Cor e Forma:SolidPeso molecular:512.591Fluvirucin A2
CAS:Fluvirucin A2 is a novel antibiotic effective against the influenza A virus.Fórmula:C24H46N2O6Cor e Forma:SolidPeso molecular:458.63Keap1-Nrf2-IN-1 TFA
Keap1-Nrf2-IN-1 TFA (compound35) is a potent inhibitor (IC50: 43 nM) protecting against acetaminophen liver damage.Fórmula:C26H25F3N2O9SCor e Forma:SolidPeso molecular:598.54Mycoversilin
CAS:<p>Mycoversilin is an antibiotic with inhibitory activity against dermatophytes and plant pathogenic fungi, but it does not exhibit activity against yeasts and bacteria. It strongly inhibits protein synthesis.</p>Fórmula:C18H16O8Cor e Forma:SolidPeso molecular:360.315BE-10988
CAS:<p>BE-10988 is a DNA topoisomerase (DNAtopoisomerase) inhibitor. It suppresses the growth of P388 murine leukemia cell lines that are resistant to Doxorubicin and Vinblastine by promoting the formation of DNA topoisomerase complexes.</p>Fórmula:C13H10N4O3SCor e Forma:SolidPeso molecular:302.31Pluracidomycin C1
CAS:Pluracidomycin C1 is a carbapenem antibiotic that exhibits activity against both Gram-positive and Gram-negative bacteria and also possesses β-lactamase inhibitory properties.Fórmula:C10H13NO10S2Cor e Forma:SolidPeso molecular:371.341CYP2C9/CYP2C19-IN-1
CYP2C9/CYP2C19-IN-1 is a potent inhibitor of CYP2C9/CYP2C19 without liver toxicity or genotoxicity and can be used to study Zika virus (ZIKV) infection.Fórmula:C27H28N2O6SCor e Forma:SolidPeso molecular:508.59TKL-IN-2
CAS:TKL-IN-2 (Compound 7m) is a TKL inhibitor with an IC50 of 0.11 mg/L against SvTKL. It exhibits excellent herbicidal activity against Digitaria sanguinalis and Amaranthus retroflexus, while being safe for corn, wheat, soybean, and cotton. TKL-IN-2 is suitable for research in weed control in crop fields.Fórmula:C23H17ClF3N3OCor e Forma:SolidPeso molecular:443.85Oudermansin B
CAS:Oudermansin B is an antibiotic that targets fungi by inhibiting the synthesis of proteins, RNA, and DNA.Fórmula:C18H23ClO5Cor e Forma:SolidPeso molecular:354.83(±)-ANAP hydrochloride (1185251-08-4 free base)
(±)-ANAP hydrochloride is the amino acid analog of prodan. It can be used as a fluorescent probes and enhance environmental sensitivity.Fórmula:C15H17ClN2O3Pureza:98%Cor e Forma:SolidPeso molecular:308.76Epithienamycin F
CAS:Epithienamycin F is a carbapenem antibiotic with activity against both Gram-positive and Gram-negative bacteria.Fórmula:C13H18N2O8S2Cor e Forma:SolidPeso molecular:394.421(R)-NVS-ZP7-4
CAS:(R)-NVS-ZP7-4, an R-isomer, inhibits ZIP7 to study ER zinc impact & Notch pathway.Fórmula:C28H28FN5OSPureza:98%Cor e Forma:SolidPeso molecular:501.62Melanocin A
CAS: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.Fórmula:C18H14N2O5Cor e Forma:SolidPeso molecular:338.31PCSK9-IN-16
CAS:<p>PCSK9-IN-16, holds potential for research into hypercholesterolemia and other cardiovascular diseases [1].</p>Fórmula:C16H20N6O2S3Cor e Forma:SolidPeso molecular:424.56Acetoxycycloheximide
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:339.38Methymycin
CAS:Methymycin is a macrolide antibiotic with activity against Gram-positive bacteria and some Gram-negative bacteria.Fórmula:C25H43NO7Cor e Forma:SolidPeso molecular:469.611TRK-IN-12
CAS:TRK-IN-12 (9e), a macrocyclic TRK inhibitor (G595R IC50=13.1 nM), outperforms LOXO-101 in Ba/F3-NTRK1 cells.Fórmula:C18H19ClFN5O3SCor e Forma:SolidPeso molecular:439.89PF-5177624
CAS:PF-5177624 is a selective and potent PDK1 inhibitor inducing anti-tumor activity in breast cancer cells.Fórmula:C25H25FN8O2Cor e Forma:SolidPeso molecular:488.52Chloronectrin
CAS:<p>Chloronectrin exhibits activity against Gram-positive bacteria.</p>Fórmula:C25H33ClO6Cor e Forma:SolidPeso molecular:464.979Anticancer agent 27
Anticancer agent 27 is a promising candidate for the treatment of cancer and deserves further development.Fórmula:C28H31NO6Cor e Forma:SolidPeso molecular:477.55Zetomipzomib
CAS:KZR-616: Immunoproteasome inhibitor targeting LMP7 (IC50: 39/57 nM) & LMP2 (IC50: 131/179 nM), potential in autoimmune disease research.Fórmula:C30H42N4O8Cor e Forma:SolidPeso molecular:586.68SPR-00305
CAS:<p>SPR-00305 is a novel potent inhibitor of the mvfr pathway</p>Fórmula:C24H19ClN2O3Cor e Forma:SolidPeso molecular:418.87SCP1-IN-1
CAS:<p>SCP1-IN-1 (SH T-62) is a potent inhibitor of SCP1, promoting REST degradation and potentially aiding glioblastoma research.</p>Fórmula:C20H19F3N2O7S2Pureza:99.53%Cor e Forma:SoildPeso molecular:520.5Milbemycin α11
CAS:<p>Milbemycin α11 (Meilingmycin A) is an antibiotic known for its ability to eliminate nematodes and mites.</p>Fórmula:C36H50O9Cor e Forma:SolidPeso molecular:626.78MRS2279
CAS:Selective, high affinity competitive antagonist of the P2Y1 receptorFórmula:C13H18ClN5O8P2Pureza:98%Cor e Forma:SolidPeso molecular:469.71Fusarielin A
CAS:Fusarielin A is a natural product found in the genus Fusarium.Fórmula:C25H38O4Cor e Forma:SolidPeso molecular:402.57SENP2-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:599.72GS-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:415.44ZK118182 isopropyl ester
CAS:ZK118182 isopropyl ester is a PG analog with potent DP-agonist activity (EC50 = 16.5 nM) and high affinity for the DP receptor (Ki = 74 nM).Fórmula:C23H37ClO5Pureza:98%Cor e Forma:SolidPeso molecular:428.99Monamycin H2
CAS:Monamycin H2 is an ester peptide antibiotic that exhibits activity against Gram-positive bacteria.Fórmula:C34H56ClN7O8Peso molecular:726.30PD-1/PD-L1-IN-17
<p>PD-1/PD-L1-IN-17 (Compound P20) is a potent PD-1/PD-L1 inhibitor (IC50: 26.8 nM).</p>Fórmula:C23H20ClN3O4Cor e Forma:SolidPeso molecular:437.88Ganciclovir monophosphonate
CAS:Ganciclovir monophosphate treats CMV, inhibiting replication in human/animal strains (IC50: 0.01μM).Fórmula:C10H16N5O6PCor e Forma:SolidPeso molecular:333.24Griseorhodin G
CAS:Griseorhodin G is a quinone antibiotic with antitumor activity.Fórmula:C25H18O12Peso molecular:510.40Polyoxin E
CAS:<p>Polyoxin E is a nucleoside antifungal antibiotic that demonstrates significant effectiveness against rice sheath blight.</p>Fórmula:C17H23N5O13Cor e Forma:SolidPeso molecular:505.395,6-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:128.13Glaucarubin
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:496.55Dihydropergillin
CAS:<p>Dihydropergillin is produced by the Aspergillus terreus strain (ATCC 38849) and has the ability to inhibit plant growth.</p>Fórmula:C15H18O4Peso molecular:262.30Papyracon 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:266.29AVE 0991
CAS:<p>AVE 0991 is a nonpeptide analog of angiotensin-(1-7), a Mas agonist with inhibitory effects on [125I]-Ang-(1-7) and on neuroinflammation in Alzheimer's disease.</p>Fórmula:C29H32N4O5S2Pureza:98.69%Cor e Forma:SolidPeso molecular:580.72Melanoxazal
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:167.16Demycarosyl platenomycin
CAS:<p>Demycarosylplatenomycin (DM-PLM) is an antibiotic that exhibits mild activity against Gram-positive bacteria.</p>Fórmula:C31H51NO11Peso molecular:613.74AY 17,605
CAS:AY 17,605 is an inhibitor of bovine heart and rat brain nucleoside-3',5'- monophosphate phosphodiesterase.Fórmula:C25H36O5Cor e Forma:SolidPeso molecular:416.55Hazimycin 6
CAS:Hazimycin 6 exhibits weak activity against gram-negative bacteria, yeast, and dermatophytes.Fórmula:C20H18N4O4Cor e Forma:SolidPeso molecular:378.381Dioxamycin
CAS:<p>Dioxamycin exhibits activity against Gram-positive bacteria and inhibits Staphylococcus aureus 209P with a minimum inhibitory concentration (MIC) of 3.12 μg/mL. It also suppresses the proliferation of L1210, P388, IMC, LX-1, and SC-6 cells with IC50 values (μg/mL) of 2.7, 1.4, 6.0, 2.0, and 2.5, respectively.</p>Fórmula:C38H40O15Cor e Forma:SolidPeso molecular:736.715Oudenone
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:208.2546-Hydroxytetrangulol
CAS:<p>6-Hydroxytetrangulol is an inducer of CPP32 protease found in Streptomyces.</p>Fórmula:C19H12O5Cor e Forma:SolidPeso molecular:320.30Saframycin Mx2
CAS:<p>Saframycin Mx2 exhibits activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C29H38N4O8Cor e Forma:SolidPeso molecular:570.634Fleephilone
CAS:Fleephilone is a fungal metabolite isolated from Trichoderma harzianum. It acts as an HIV REV/RRE binding inhibitor, hindering the interaction between REV protein and RRE RNA with an IC50 of 7.6 μM.Fórmula:C24H27NO7Cor e Forma:SolidPeso molecular:441.474Hypercalin B
CAS:<p>Hypercalin B is an antibacterial agent isolated from the hexane and chloroform extracts of Hypericum acmosepalum. It demonstrates activity against multidrug-resistant strains of Staphylococcus aureus, with a minimum inhibitory concentration (MIC) ranging from 0.5 to 128 mg/L.</p>Fórmula:C33H42O5Cor e Forma:SolidPeso molecular:518.684U 80215
CAS:<p>U 80215 is an enzyme-competitive inhibitor.</p>Fórmula:C42H60N8O6SCor e Forma:SolidPeso molecular:805.04JTE 151A
CAS:JTE-151 is a novel RORγ inverse agonist.Fórmula:C26H30ClN3O5Cor e Forma:SolidPeso molecular:499.99MU1656
CAS:<p>MU1656 is a selective inhibitor of histone methyltransferase DOT1L, which significantly inhibits cancer cell proliferation in hematological malignancies.</p>Fórmula:C32H45N7O2Pureza:96.92%Cor e Forma:SolidPeso molecular:559.759-Hydroxycrisamicin
CAS:9-Hydroxycrisamicin exhibits moderate activity against Gram-positive bacteria with a minimum inhibitory concentration (MIC) ranging from 6.25 to 25 μg/mL. Additionally, 9-Hydroxycrisamicin demonstrates significant growth inhibition towards various human tumor cell lines.Fórmula:C32H22O13Cor e Forma:SolidPeso molecular:614.51Antitumor agent-65
CAS:Antitumor agent-65 (Compound 5) is an analogue/derivative of (-)-cleistenolide. Antitumor agent-65 has potential in cancer research.Fórmula:C18H17NO10Cor e Forma:SolidPeso molecular:407.33ZK824859 hydrochloride (2271122-53-1 free base)
ZK824859 hydrochloride: oral, selective uPA inhibitor, IC50s: 79 nM (uPA), 1580 nM (tPA), 1330 nM (plasmin).Fórmula:C23H23ClF2N2O4Pureza:98%Cor e Forma:SolidPeso molecular:464.89Glucosylceramide synthase-IN-3
Glucosylceramide synthase-IN-3 (BZ1) is a potent, brain-accessible, oral GCS inhibitor with a 16 nM IC50, relevant for Gaucher's disease study.Fórmula:C21H20FN3O3Cor e Forma:SolidPeso molecular:381.4Antileishmanial agent-6
<p>Antileishmanial agent-6: potent against Leishmania donovani, IC50 0.54μM; cytotoxic IC50 10.2μM.</p>Fórmula:C24H26O8Cor e Forma:SolidPeso molecular:442.46KT2-962
CAS:<p>KT2-962 is a TXA2/prostaglandin endoperoxide receptor antagonist.</p>Fórmula:C23H27ClNNaO5S2Cor e Forma:SolidPeso molecular:520.04Matlystatin F
CAS:<p>Matlystatin F is an inhibitor of metalloproteinases (MMP).</p>Fórmula:C27H44N6O6Cor e Forma:SolidPeso molecular:548.675Leucomycin A6
CAS:<p>Leucomycin A6 effectively combats Gram-positive bacteria.</p>Fórmula:C41H67NO14Cor e Forma:SolidPeso molecular:797.969Unoprostone
CAS:Unoprostone is a prostaglandin F2α analogs (PGAs), and reduces intraocular pressure and is used topically for glaucoma or ocular hypertension.Fórmula:C22H38O5Pureza:98%Cor e Forma:SolidPeso molecular:382.53Atiratecan
CAS:Atiratecan (TP300), a CH0793076-based camptothecin prodrug, combats BCRP+/- tumors; doesn't affect AChE.Fórmula:C31H34N6O6Pureza:98%Cor e Forma:SolidPeso molecular:586.64Thielavin B
CAS:Thielavin B, from Thielavia terricola, inhibits prostaglandin E2 synthesis and reduces rat oedema.Fórmula:C31H34O10Cor e Forma:SolidPeso molecular:566.6Luffolide
CAS:Luffolide, a Luffariella sponge metabolite, shares manoalide's anti-inflammatory traits and fully inhibits PLA2's cleavage of phosphatidylcholine.Fórmula:C27H40O6Cor e Forma:SolidPeso molecular:460.60FK-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:790.44SAR107375
CAS:<p>SAR107375 is a potent, orally active dual inhibitor of thrombin and factor Xa, with K_i values of 1 nM and 8 nM for factor Xa and thrombin, respectively [1].</p>Fórmula:C24H30ClN5O5S2Cor e Forma:SolidPeso molecular:568.11Azirinomycin
CAS:<p>Azirinomycin exhibits activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C4H5NO2Cor e Forma:SolidPeso molecular:99.088Darlucin B
CAS:<p>Darlucin B exhibits both antibacterial and antifungal properties, and it possesses mild cytotoxicity.</p>Fórmula:C19H20N2O3Cor e Forma:SolidPeso molecular:324.374Seldomycin 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:454.473Hymenidin
CAS:Hymenidin, isolated from the Okinawan sponge Hymeniacidon sp., is a 5-hydroxytryptaminergic receptor antagonist and voltage-gated potassium channel inhibitor.Fórmula:C11H12BrN5OPureza:96.85% - 99.52%Cor e Forma:SolidPeso molecular:310.15Miyakamide B1
CAS:<p>Miyakamide B1 is an antibiotic with insecticidal properties, capable of inhibiting the growth of brine shrimp. It displays moderate activity against Xanthomonas bacteria and inhibits P388 cells with an IC50 of 8.8 μg/mL.</p>Fórmula:C31H32N4O4Cor e Forma:SolidPeso molecular:524.613HKT-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:311.131Coleon-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:344.4JBIR-22
CAS:<p>JBIR-22 is a natural inhibitor for protein−protein interaction of the homodimer of proteasome assembly factor 3.</p>Fórmula:C23H33NO6Cor e Forma:SolidPeso molecular:419.51Rivenprost
CAS:Rivenprost, selective EP4 agonist (Ki: 0.7 nM), promotes bone growth, osteoblast differentiation, and aids wound healing.Fórmula:C24H34O6SCor e Forma:SolidPeso molecular:450.59Antiviral agent 6
<p>Antiviral agent 6 showed excellent anti-TSWV effects in vivo (EC50: 188 mg/L).</p>Fórmula:C23H27BrN2O3S2Cor e Forma:SolidPeso molecular:523.51A 74273
CAS:<p>A 74273, a nonpeptidic and renin inhibitor, may be used to treat cardiovascular diseases due to renin inhibition.</p>Fórmula:C44H74N4O8Pureza:98%Cor e Forma:SolidPeso molecular:787.08J-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:531.60Epiderstatin
CAS:<p>Epiderstatin is isolated from Streptomyces pulveraceus subsp. epiderstagenes; inhibits mitogenic activity of epidermal growth factor.</p>Fórmula:C15H20N2O4Cor e Forma:SolidPeso molecular:292.33NTPDase-IN-3
CAS:NTPDase-IN-3 inhibits NTPDase1/2/3/8 (IC50: 0.21/1.07/0.38/0.05 μM), useful for cancer and thrombosis research.Fórmula:C22H24ClN3OS2Cor e Forma:SolidPeso molecular:446.03LY 190388
CAS:<p>LY 190388 is a penicillamine-containing enkephalin analog used as an mu receptor agonist with analgesia activity.</p>Fórmula:C30H41N5O7SPureza:98%Cor e Forma:SolidPeso molecular:615.74Emd 52297
CAS:<p>Emd 52297 is an inhibitor of renin.</p>Fórmula:C39H59N11O7Pureza:98%Cor e Forma:SolidPeso molecular:793.96AFP-07 free acid
CAS:AFP 07 free acid is a 7,7-difluoroprostacyclin derivative. It also acts as a selective and highly potent agonist for the IP receptor.Fórmula:C22H30F2O5Pureza:98%Cor e Forma:SolidPeso molecular:412.47WAY-855
CAS:WAY-855 is an EAAT2-preferring, nonsubstrate inhibitor of high-affinity glutamate uptake.Fórmula:C9H11NO4Cor e Forma:SolidPeso molecular:197.19Anticancer agent 26
<p>Anticancer agent 26 is a promising candidate for cancer therapy and deserves further development.</p>Fórmula:C28H33NO5Cor e Forma:SolidPeso molecular:463.57OncoFAP
CAS:<p>OncoFAP is an ultra-high affinity fibroblast activating protein (FAP) ligand with potential tumour targeting.</p>Fórmula:C21H19F2N5O5Pureza:99.77%Cor e Forma:SolidPeso molecular:459.40Nafarelin 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·xH2OCor e Forma:SolidPeso molecular:1400.563CH5447240
CAS:<p>CH5447240: potent hPTHR1 agonist, treats Hypoparathyroidism, EC50 12 nM, 55% oral bioavailability, raises rat serum calcium.</p>Fórmula:C26H39N5O4SPureza:98%Cor e Forma:SolidPeso molecular:517.68KMN-80
CAS:<p>KMN-80 is a potent, selective EP4 agonist with IC50 3 nM, spurring osteoblast differentiation, and showing in vivo bone repair efficacy.</p>Fórmula:C21H33NO4Cor e Forma:SolidPeso molecular:363.49Detoxin D1
CAS:<p>Detoxin D1 is a selective blasticidin S antagonist.</p>Fórmula:C28H41N3O8Pureza:98%Cor e Forma:SolidPeso molecular:547.64Foroxymithine
CAS:Foroxymithine is an inhibitor of angiotensin-converting enzyme.Fórmula:C22H37N7O11Pureza:98%Cor e Forma:SolidPeso molecular:575.57MDK6465
CAS:MDK6465 (PCSK9-IN-8b), CAS#1900686-46-5, is a liver-targeted PCSK9 synthesis inhibitor.Fórmula:C27H29ClFN9O4Cor e Forma:SolidPeso molecular:598.03Anticancer agent 17
Anticancer agent 17 was effective against HeLa cells (IC50: 0.19 μM) and A2780 cells (IC50: 0.09 μM).Fórmula:C27H34BrN3OCor e Forma:SolidPeso molecular:496.48De-N-methylpamamycin-593A
CAS:De-N-methylpamamycin-593A is a 16-membered macrocyclic dilactone known for its ability to induce aerial mycelium formation.Fórmula:C34H59NO7Peso molecular:593.84Flurdihydroergotamine
CAS:Flurdihydroergotamine, a serotonin 5HT1 receptor agonist, is used as an antimigraine drug.Fórmula:C34H36F3N5O5Pureza:98%Cor e Forma:SolidPeso molecular:651.68Monamycin G1
CAS:<p>Monamycin G1 is an ester-peptide antibiotic [esterpeptid]. It shows activity against Gram-positive bacteria.</p>Fórmula:C33H54ClN7O8Peso molecular:712.28SMP-797 HCl
CAS:SMP-797 HCl, an ACAT (acyl-CoA-cholesterol acyltransferase) inhibitor, is used potentially for the treatment of Hyperlipidemia.Fórmula:C34H44ClN5O4Pureza:98%Cor e Forma:SolidPeso molecular:622.20RMI-18341
CAS:RMI-18341 is a Testosterone 5 alpha reductase inhibitor.Fórmula:C22H34N2O2Cor e Forma:SolidPeso molecular:358.52Oryzoxymycin
CAS:<p>Oryzoxymycin is an aromatic derivative antibiotic with activity against Gram-negative bacteria.</p>Fórmula:C10H13NO5Peso molecular:227.21Lucilactaene
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:401.45Norplicacetin
CAS:<p>Norplicacetin exhibits activity against Gram-positive bacteria and mycobacteria.</p>Fórmula:C24H33N5O7Peso molecular:503.55Polyoxin L
CAS:<p>Polyoxin L is a nucleoside-type antifungal antibiotic that is notably effective against rice sheath blight.</p>Fórmula:C16H23N5O12Peso molecular:477.38AL 6598
CAS:AL 6598, a prodrug of PGD2 agonist AL 6556, reduces IOP by 53% at 1μg twice daily in monkeys; binds DP receptors with Ki of 3.2μM.Fórmula:C23H39ClO5Cor e Forma:SolidPeso molecular:431.01KY-02327 acetate
KY-02327 acetate inhibits Dvl-CXXC5, stabilizes Wnt/β-catenin signaling, and enhances osteoblast differentiation.Fórmula:C22H31N3O6Cor e Forma:SolidPeso molecular:433.5(rel)-Myrislignan
CAS:(rel)-Myrislignan, a lignan compound with a relative configuration, has been isolated from Myristica fragrans Houtt.Fórmula:C21H26O6Pureza:98%Cor e Forma:SolidPeso molecular:374.43Herbicidin B
CAS:Herbicidin B exhibits herbicidal properties and activity against Gram-positive bacteria.Fórmula:C18H23N5O9Cor e Forma:SolidPeso molecular:453.403Pentenocin A
CAS:<p>Pentenocin A exhibits a relatively weak inhibitory effect on IL-1 and β-glucuronidase (ICE) activity.</p>Fórmula:C7H10O5Cor e Forma:SolidPeso molecular:174.151Harziphilone
CAS:<p>Harziphilone exhibits mild activity against Gram-positive bacteria and possesses antitumor properties, showing inhibitory effects on lymphocytic leukemia L1210 and leukemia P388 with an IC50 of 0.26 μg/mL. Additionally, Harziphilone inhibits the binding of the Rev protein to [33P]-labeled Rev response element (RRE) RNA, with an IC50 of 2.0 μM.</p>Fórmula:C15H18O4Cor e Forma:SolidPeso molecular:262.3013,4-Dimethoxytropolone
CAS: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.Fórmula:C9H10O4Cor e Forma:SolidPeso molecular:182.173GC 14
CAS:GC 14 is a selective thyroid hormone receptor antagonist, with IC50 values of 200 nM and 35 nM for hTRα and hTRβ, respectively.Fórmula:C26H27NO6Pureza:98%Cor e Forma:SolidPeso molecular:449.5L 731735
CAS:L 731735 is a farnesyltransferase inhibitor.Fórmula:C19H40N4O4SPureza:98%Cor e Forma:SolidPeso molecular:420.61Mycinamicin Ⅵ
CAS:<p>Mycinamicin VI is a macrolide antibiotic with antibacterial activity against Gram-positive bacteria.</p>Fórmula:C35H57NO11Cor e Forma:SolidPeso molecular:667.83Megovalicin G
CAS:Megovalicin G is effective against Bacillus subtilis and Escherichia coli, and it also acts on Pseudomonas aeruginosa.Fórmula:C35H61NO7Cor e Forma:SolidPeso molecular:607.86Monamycin B
CAS:Monamycin B is an ester peptide antibiotic with activity against Gram-positive bacteria.Fórmula:C33H55N7O8Cor e Forma:SolidPeso molecular:677.83FR-900482
CAS: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.Fórmula:C14H15N3O6Cor e Forma:SolidPeso molecular:321.29Dictyopanine A
CAS:Dictyopanine A exhibits a relatively narrow antibacterial spectrum, demonstrating moderate antimicrobial activity only against certain filamentous fungi and Gram-positive bacteria.Fórmula:C25H34O5Cor e Forma:SolidPeso molecular:414.53(S)-5-hydroxy-6-methoxy Duloxetine maleate
(S)-5-hydroxy-6-methoxy Duloxetine, an active metabolite of the (S)-duloxetine, functions as a serotonin (5-HT) and norepinephrine reuptake inhibitor.Fórmula:C19H21NO3S·C4H4O4Cor e Forma:SolidPeso molecular:459.51RIP1 kinase inhibitor 1
CAS:RIP1 kinase inhibitor 1 is an orally available and brain-penetrating inhibitor of RIP1 kinase with pKi of 9.04.Fórmula:C24H20ClN5O3Pureza:98%Cor e Forma:SolidPeso molecular:461.95-Deoxygentamicin C1
CAS:5-Deoxygentamicin C1 exhibits activity against both gram-positive and gram-negative bacteria.Fórmula:C21H43N5O6Cor e Forma:SolidPeso molecular:461.60Pralatrexate, (R)-
CAS:Pralatrexate is a high-affinity DHFR inhibitor targeting RFC-1, used in cancer treatment and immunosuppression.Fórmula:C23H23N7O5Pureza:98%Cor e Forma:SolidPeso molecular:477.47ROPA
CAS:ROPA, a potent PKCalpha and PKCgamma activator, promotes tumor growth through PKC-activation.Fórmula:C28H32O6Pureza:98%Cor e Forma:SolidPeso molecular:464.55Squalestatin 2
CAS:<p>Squalestatin 2 is an inhibitor of squalene synthase.</p>Fórmula:C33H44O13Pureza:98%Cor e Forma:SolidPeso molecular:648.69Cinnatriacetin A
CAS:<p>Cinnatriacetin A exhibits activity against Gram-positive bacteria.</p>Fórmula:C23H20O5Cor e Forma:SolidPeso molecular:376.402Coriolin A
CAS:<p>Coriolin A exhibits activity against gram-positive bacteria, weakly against gram-negative bacteria, as well as yeasts and Trichomonas vaginalis. At a concentration of 5 μg/mL, it inhibits 61.6% of the growth of Yoshida sarcoma, but shows no inhibitory effect on Ehrlich ascites carcinoma in animals.</p>Fórmula:C15H20O5Cor e Forma:SolidPeso molecular:280.316ZBH-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:C29H31N3O8Cor e Forma:SolidPeso molecular:549.57Griseolic acid C
CAS: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).Fórmula:C14H15N5O7Cor e Forma:SolidPeso molecular:365.298Cryptopleurine
CAS:Cryptopleurine is an inhibitor of gene products associated with cell proliferation, survival, invasion and angiogenesis. It acts by targeting the NF-κB pathway.Fórmula:C24H27NO3Pureza:98%Cor e Forma:SolidPeso molecular:377.48P-gp modulator 2
P-gp modulator 2 (Compound 27) is a potent competitive and metabotropic P-glycoprotein (P-gp) modulator.Fórmula:C22H20BrN3O4Cor e Forma:SolidPeso molecular:470.32NA 0346
CAS:NA 0346 is a derivative of SF 2370 that shows long lasting antihypertensive action as well as potent protein kinases inhibitory activity.Fórmula:C26H22N4O3Cor e Forma:SolidPeso molecular:438.48Rhodomycin B
CAS:<p>Rhodomycin B exhibits activity against Gram-positive bacteria, while its effects on Gram-negative bacteria and fungi are relatively weak.</p>Fórmula:C28H33NO10Cor e Forma:SolidPeso molecular:543.562Saframycin B
CAS:<p>Saframycin B exhibits activity against Gram-positive bacteria and has weaker efficacy against mycobacteria.</p>Fórmula:C28H31N3O8Cor e Forma:SolidPeso molecular:537.561Salfredin C1
CAS:<p>Salfredin C1 is an inhibitor of aldose reductase.</p>Fórmula:C13H11NO6Cor e Forma:SolidPeso molecular:277.229Diatretyne Ⅰ
CAS:Diatretyne I (Diatretyne amide) exhibits mild activity against Gram-positive bacteria.Fórmula:C8H5NO3Cor e Forma:SolidPeso molecular:163.13Anticancer 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:C27H33N5O6Cor e Forma:SolidPeso molecular:523.58Kurasoin A
CAS:<p>Kurasoin A is an inhibitor of the enzyme farnesyltransferase.</p>Fórmula:C16H16O3Cor e Forma:SolidPeso molecular:256.296Piloquinone
CAS:<p>Piloquinone is a type of phenanthrene compound that exhibits mild inhibitory effects on mycobacteria and protozoa.</p>Fórmula:C21H20O5Cor e Forma:SolidPeso molecular:352.38ZK159222
CAS:ZK159222 is an effective 1α,25-(OH)2D3 receptor (VDR) agonist. ZK159222 has a partial agonistic character.Fórmula:C32H48O5Pureza:98%Cor e Forma:SolidPeso molecular:512.72DMGF
CAS:DMGF, a biflavonoid from Taxus, induces apoptosis, autophagy, and inhibits B16F10 cell motility and MMP-2 expression, hindering melanoma metastasis.Fórmula:C32H22O10Cor e Forma:SolidPeso molecular:566.51DNDI-8219
CAS:DNDI-8219 is an antitubercular agent. It has potent antileishmanial effects.Fórmula:C13H10F3N3O5Cor e Forma:SolidPeso molecular:345.23PI4KIIIbeta-IN-11
CAS:PI4KIIIbeta-IN-11 is a PI4KIIIβ inhibitor (mean pIC50=9.1) that can be used to study diseases caused by RNA viruses and Plasmodium falciparum.Fórmula:C33H39N7O3Cor e Forma:SolidPeso molecular:581.71MDL-100173
CAS:<p>MDL-100173 is a dual angiotensin-converting enzyme (ACE)/neutral endopeptidase (NEP) inhibitor.</p>Fórmula:C24H26N2O4SCor e Forma:SolidPeso molecular:438.549-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:276.328Hydrolyzed Fumonisin B2
CAS:Hydrolyzed Fumonisin B2 (HFB2) is a hydrolysis product of fumonisins (HF), which retains biological activity. It exhibits phytotoxicity.Fórmula:C22H47NO4Pureza:98%Cor e Forma:SolidPeso molecular:389.61Gilvusmycin
CAS:<p>Gilvusmycin is an antibiotic with potent antitumor properties. It effectively inhibits the proliferation of P388, K562, A431, and MKN28 cells, with IC50 values (ng/mL) of 0.08, 0.86, 0.72, and 0.75, respectively.</p>Fórmula:C38H34N6O8Cor e Forma:SolidPeso molecular:702.7122-Hydroxy-5-iminoazacyclopent-3-ene
CAS:<p>2-Hydroxy-5-iminoazacyclopent-3-ene is a pyrroline-class antibiotic with mild activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C4H6N2OCor e Forma:SolidPeso molecular:98.103Memnobotrin A
CAS:Memnobotrin A is an antibiotic with inhibitory effects on the NCI-460, MCF7, and SF-268 cell lines.Fórmula:C25H33NO5Cor e Forma:SolidPeso molecular:427.53Disorazol A
CAS:Disorazol A1 is a tubulin inhibitor with antifungal properties. It functions by inhibiting tubulin polymerization and disrupting microtubule formation, thereby blocking mitosis and arresting the cell cycle at the G2/M phase, which induces apoptosis. Disorazol A1 also inhibits L929 mouse fibroblasts with an IC50 value of 3 pm and causes accumulation of p53 protein in the nucleus. Disorazol A1 holds potential for cancer research.Fórmula:C43H54N2O10Cor e Forma:SolidPeso molecular:758.896Chrymutasin C
CAS:Chrymutasin C is a glycoside antitumor antibiotic with cytotoxic properties.Fórmula:C39H43NO17Cor e Forma:SolidPeso molecular:797.755MB-07344 sodium
"MB-07344 sodium is a TR-β agonist with a 2.17 nM Ki, boosts Atorvastatin's cholesterol-lowering effects in various animals."Fórmula:C19H25NaO5PPureza:98%Cor e Forma:SolidPeso molecular:387.36Menoxymycin 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:C24H27NO9Cor e Forma:SolidPeso molecular:473.473ZIKV-IN-5
ZIKV-IN-5 is an acid-stable, low cytotoxic anti-ZIKV agent with an EC50 value of 0.71 μM. ZIKV-IN-5 showed effective inhibition of ZIKV NS5 MTase activity.Fórmula:C36H45NO4SiCor e Forma:SolidPeso molecular:583.83TP-030-2
CAS:<p>TP-030-2 is a RIPK1 inhibitor (human K i =0.43 nM ; mouse IC 50 =100 nM) .</p>Fórmula:C23H21BrN4O3Cor e Forma:SolidPeso molecular:481.34Antimalarial 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:471.5Resorcinomycin B
CAS:<p>Resorcinomycin B is an antibiotic found in [Streptoverticillum roseoverticillatum].</p>Fórmula:C13H18N4O5Cor e Forma:SolidPeso molecular:310.306SGK1-IN-3
SGK1-IN-3: Potent oral inhibitor of SGK1, may target osteoarthritis.Fórmula:C23H20Cl2N6O3SCor e Forma:SolidPeso molecular:531.41Imolamine hydrochloride
CAS:Imolamine hydrochloride is a blood platelet aggregation antagonist.Fórmula:C14H21ClN4OCor e Forma:SolidPeso molecular:296.80(±)-HIP-B
CAS:(±)-HIP-B is an excitatory amino acid transporter blocker.Fórmula:C6H8N2O4Pureza:98%Cor e Forma:SolidPeso molecular:172.14NCI-006
CAS:<p>NCI-006, an LDH inhibitor, slows tumor growth and enhances pyruvate's role in mitochondrial metabolism.</p>Fórmula:C31H24F2N4O4S3Cor e Forma:SolidPeso molecular:650.74Polyoxin H
CAS:Polyoxin H is a nucleoside antifungal antibiotic that exhibits significant efficacy against rice sheath blight.Fórmula:C23H32N6O13Cor e Forma:SolidPeso molecular:600.53Pterulinic acid
CAS:<p>Pterulinic acid is an inhibitor of coenzyme I:coenzyme Q oxidoreductase. It demonstrates IC50 values (μg/mL) of 50 for the mammalian cell line L1210, 20 for HL60, 25 for HeLaS3, and 100 for BHK.</p>Fórmula:C15H11ClO4Cor e Forma:SolidPeso molecular:290.70Ep vinyl quinidine
CAS:3-Epiquinine is a Quinidine stereoisomer, used in malaria, antiarrhythmic, inhibits P450db, and blocks K+ channels, IC50: 19.9 μM.Fórmula:C20H24N2O2Cor e Forma:SolidPeso molecular:324.42MB725
CAS:MB725 is a strong and selective inducer of viability reduction in several cancer cell lines containing the oncogenic p53-Y220C mutation.Fórmula:C18H21IN4O2SCor e Forma:SolidPeso molecular:484.35SK&F 108361
CAS:SK&F 108361 is a symmetric diol that binds HIV-1 protease symmetrically.Fórmula:C24H48N6O6Cor e Forma:SolidPeso molecular:516.67Antibiotic LL Z1640-2
CAS:Antibiotic LL Z1640-2 is an inhibitor against the TAK1 activity.Fórmula:C19H22O7Cor e Forma:SolidPeso molecular:362.38Cytosaminomycin B
CAS:<p>Cytosaminomycin B exhibits activity against Eimeria Tenella coccidia.</p>Fórmula:C26H37N5O8Cor e Forma:SolidPeso molecular:547.601AN-12-H5
CAS:AN-12-H5 is an anti-enteroviral compound that targets the replication process of PV and EV71 viruses.Fórmula:C24H23N3O4S3Cor e Forma:SolidPeso molecular:513.65Glisoprenin E
CAS:Glisoprenin E is an inhibitor of acyl-CoA:cholesterol acyltransferase (ACAT) that can prevent the formation of hydrophobic surface adhesion cells in Pyricularia oryzae.Fórmula:C45H86O9Cor e Forma:SolidPeso molecular:771.16Porothramycin B
CAS:Porothramycin B is an antibiotic with activity against Gram-positive bacteria and anaerobes.Fórmula:C19H23N3O4Cor e Forma:SolidPeso molecular:357.404Asperenone
CAS:Asperenone is a 15-lipoxygenase (15-LOX) inhibitor with an IC50 of 0.3 mM. Additionally, it acts as a platelet aggregation inhibitor with an IC50 of 0.23 mM. Asperenone also exhibits antifungal properties, inhibiting the growth of pathogenic fungi Ophiostoma crassivaginatum and O. piliferum, and may be utilized in research related to cardiovascular diseases and anti-infective treatments.Fórmula:C20H22OCor e Forma:SolidPeso molecular:278.388Cytosaminomycin C
CAS:<p>Cytosaminomycin C exhibits anti-Eimeria Tenella coccidial activity.</p>Fórmula:C23H36N4O8Cor e Forma:SolidPeso molecular:496.554Haliangicin 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:163.216Epelmycin D
CAS:Epelmycin D exhibits activity against both Gram-positive and Gram-negative bacteria, as well as Candida albicans, and demonstrates efficacy against leukemia (L1210).Fórmula:C30H35NO11Cor e Forma:SolidPeso molecular:585.599Pluracidomycin C2
CAS:<p>Pluracidomycin C2 is a carbapenem antibiotic with activity against both Gram-positive and Gram-negative bacteria.</p>Fórmula:C11H15NO9S2Cor e Forma:SolidPeso molecular:369.37Haliangicin 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:243.34Formadicin A
CAS:<p>Formadicin A exhibits strong activity against various Pseudomonas, Proteus, and Alcaligenes bacteria.</p>Fórmula:C30H34N4O16Cor e Forma:SolidPeso molecular:706.608STA 2
CAS:STA 2 is an analogue of TXA2, a thromboxane receptor in the colonic epithelium.Fórmula:C21H34O3SCor e Forma:SolidPeso molecular:366.5611-Demethyltomaymycin
CAS:<p>11-Demethyltomaymycin is an antibiotic that exhibits antiviral activity against Escherichia coli T1 and T3 bacteriophages, along with antibacterial properties against Gram-positive bacteria. Furthermore, it shows cytotoxic effects on leukemia L1210 cells.</p>Fórmula:C15H18N2O4Cor e Forma:SolidPeso molecular:290.314Halomicin D
CAS:Halomicin D is an ansamycin-class antibiotic that exhibits activity against both Gram-positive and Gram-negative bacteria.Fórmula:C43H56N2O12Cor e Forma:SolidPeso molecular:792.911Lactoquinomycin B
CAS:<p>Lactoquinomycin B is a quinone antibiotic with activity against Gram-positive bacteria and some Gram-negative bacteria, though its efficacy against Gram-negative species is weaker and it does not affect fungi. It inhibits various cell lines, including lymphoma L5178Y parental cells, doxorubicin-resistant cells, bleomycin-resistant cells, human leukemia K562 cells, and murine leukemia L-1210 and P388 cells, with ID50 (μg/mL) values of 0.43, 0.21, 0.19, 0.16, 0.2, and 0.12, respectively.</p>Fórmula:C24H27NO9Cor e Forma:SolidPeso molecular:473.473Juglomycin B
CAS:<p>Juglomycin B exhibits broad-spectrum antibacterial and antimycobacterial properties and is capable of inhibiting Ehrlich ascites carcinoma in mice.</p>Fórmula:C14H10O6Cor e Forma:SolidPeso molecular:274.226LAF-153
CAS:LAF-153 is a reversible Methionine Aminopeptidase‑2 (MetAP-2) Inhibitor.Fórmula:C18H32N2O7Cor e Forma:SolidPeso molecular:388.46MK-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:779.94Mutatochrome
CAS:<p>Mutatochrome (Citroxanthin) is a compound found in plants.</p>Fórmula:C40H56OCor e Forma:SolidPeso molecular:552.872Chitinovorin 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:416.406
