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Endet am 31. Dez.( 7 verbleibende Tage )
EGIS-8332
CAS:<p>EGIS-8332: potent, selective AMPA antagonist, blocks AMPA/kainate channels, protects neurons, potential for epilepsy/stroke treatment.</p>Formel:C20H18N4O3Farbe und Form:SolidMolekulargewicht:362.38EGFR-IN-451
CAS:EGFR-IN-451 is an EGFR inhibitor, attenuating Ang II-induced Kidney Fibrosis.Formel:C19H15N5OFarbe und Form:SolidMolekulargewicht:329.36ABT-925 fumarate
CAS:ABT-925/A-37203 is a selective DRD3 antagonist, with ~100x more affinity for D₃ over D₂, tested in schizophrenia.Formel:C24H31F3N6O5SFarbe und Form:SolidMolekulargewicht:572.6NNL-2
CAS:<p>NNL-2 is a synthetic cannabinoid and T-type calcium channel inhibitor. This product is for research use only.</p>Formel:C25H30FN3OFarbe und Form:SolidMolekulargewicht:407.52Nudifloric Acid
CAS:1-Methyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid (Nudifloric Acid) is from Cordyceps bassiana. Nudifloric Acid has an anti-inflammatory function.Formel:C7H7NO3Reinheit:99.55%Farbe und Form:SolidMolekulargewicht:153.14N-2733 HCl
CAS:N-2733 HCl is a nuclear factor (NF)-kappaB activation inhibitor.Formel:C12H13ClN2O2Farbe und Form:SolidMolekulargewicht:252.7AGI25696
CAS:AGI-25696, a MATA2 inhibitor, treats cancer and works on MTAP null tumors. Correct CAS# 2201065-84-9; often mistaken for #2201066-35-3.Formel:C28H20N4OFarbe und Form:SolidMolekulargewicht:428.48AFN941
CAS:AFN941 is a staurosporine analog, acting as a Jak3-specific inhibitor.Formel:C28H30N4O3Farbe und Form:SolidMolekulargewicht:470.56AZD-6126
CAS:AZD6126 (ANG-453), a water-soluble prodrug converted to N-acetylcolchinol in vivo, potentially treats solid tumors by inhibiting angiogenesis and tubulin.Formel:C20H24NO8PFarbe und Form:SolidMolekulargewicht:437.38Neramexane Free Base
CAS:Neramexane is a memantine-related, NMDA-blocking, neuroprotective drug, potentially treating tinnitus, Alzheimer's, addiction, and pain.Formel:C11H23NFarbe und Form:SolidMolekulargewicht:169.31SB-284851-BT
CAS:<p>SB-284851-BT: BRD4/p38α/BRDT inhibitor; IC50: BRD4-BD1 1.7µM, BRDT 18µM, BRD4 3.7µM; Kd p38α 0.47nM; reduces IL-8, affects c-Myc/NF-κB.</p>Formel:C26H26FN5OFarbe und Form:SolidMolekulargewicht:443.52ATZ-1993
CAS:ATZ-1993 is an Endothelin Receptor Antagonist.Formel:C28H28N4O4Farbe und Form:SolidMolekulargewicht:484.55Eprociclovir Na
CAS:Eprociclovir Na (A-5021) is 15x stronger than acyclovir at inhibiting herpesviruses, showing promise for EHV1 and herpetic keratitis treatment.Formel:C11H14N5NaO3Farbe und Form:SolidMolekulargewicht:287.25GNTI TFA
CAS:GNTI TFA is a selective kappa opioid receptor antagonist.Formel:C31H31F6N5O7Farbe und Form:SolidMolekulargewicht:699.60SGI-7079
CAS:<p>SGI-7079: selective Axl inhibitor; hinders tumor growth dose-dependently; may target EGFR inhibitor resistance.</p>Formel:C26H26FN7Reinheit:95.51% - 99.26%Farbe und Form:SolidMolekulargewicht:455.53USP7-IN-4
CAS:<p>USP7-IN-4 is a non-competitive, potent and selective inhibitor of USP7, up-regulates p53 and p21, down-regulates MDM2,anti-proliferativity RS4;11 (leukemia) .</p>Formel:C29H34N6O3Reinheit:98.27% - 99.09%Farbe und Form:SolidMolekulargewicht:514.62AMP423
CAS:AMP423, a naphthyl 2-cyanoaziridine-1-carboxamide, resembles imexon and inhibits myeloma and lymphoma tumor growth in SCID mice without myelosuppression.Formel:C14H11N3OFarbe und Form:SolidMolekulargewicht:237.26Ritlecitinib tosylate
CAS:Ritlecitinib (PF-06651600) is a potent, selective JAK3 inhibitor with proven in vivo efficacy, low clearance, and has undergone clinical trials.Formel:C22H27N5O4SFarbe und Form:SolidMolekulargewicht:457.549MC4
CAS:<p>MC4 is a first-in-class inhibitor of ribosomal RNA synthesis with antimicrobial activity against Staphylococcus aureus.</p>Formel:C15H10N2O3Farbe und Form:SolidMolekulargewicht:266.25PSB-17365
CAS:PSB-17365: powerful GPR84 agonist, EC50 of 2.5nM in cAMP, 100nM in β-arrestin 2 assay, selective over FFAR1/4, key in inflammation and cancer.Formel:C12H12BrN3O2Farbe und Form:SolidMolekulargewicht:310.15Dexetimide HCl
CAS:Dexetimide HCl is a muscarinic antagonist that has been used to treat neuroleptic-induced parkinsonism. Benzetimide is the (-)-enantimorph of dexetimide.Formel:C23H27ClN2O2Farbe und Form:SolidMolekulargewicht:398.93(2Z,3Z)-U0126
CAS:U0126 selectively inhibits MEK1/2, blocks MAPK/ERK signaling, and suppresses Ki-ras-induced cell growth, with IC50s of 72 nM and 58 nM for MEK1/2.Formel:C18H16N6S2Farbe und Form:SolidMolekulargewicht:380.49GPA-1734 bromide
CAS:GPA-1734 bromide is an inhibitor of basement membrane collagen synthesis and angiogenesis.Formel:C14H12BrNO2Farbe und Form:SolidMolekulargewicht:306.16GCN2iB acetate
CAS:<p>GCN2iB inhibits GCN2, sensitizing certain cancer cells to L-asparaginase treatment.</p>Formel:C20H16ClF2N5O5SFarbe und Form:SolidMolekulargewicht:511.8848Sildenafil Mesylate
CAS:Sildenafil Mesylate is a mesylate form of Sildenafil, an inhibitor of Phosphodiesterase 5.Formel:C22H30N6O4S·xCH4O3SReinheit:99.84%Farbe und Form:SolidMolekulargewicht:570.68GSK2239633
CAS:GSK2239633: potent CCR4 antagonist, pIC50=7.9, promising for asthma due to T-helper 2 recruitment role.Formel:C21H19ClN4O5S2Farbe und Form:SolidMolekulargewicht:506.98RPR-200765A Mesylayte
CAS:RPR-200765A selectively inhibits p38 MAP kinase, blocks TNFalpha in vitro (EC50 = 110 nM) and in mice (ED50 = 6 mg/kg), and shows promise in RA treatment.Formel:C24H25FN4O4Farbe und Form:SolidMolekulargewicht:452.48RPR203494
CAS:RPR203494 is a pyrimidine analogue of the p38 inhibitor RPR200765A with an improved in vitro potency.Formel:C26H29FN6O4Farbe und Form:SolidMolekulargewicht:508.54Xanthalin
CAS:<p>Xanthalin from Angelica purpurascens inhibits cholinesterase and carbonic anhydrase.</p>Formel:C24H26O7Farbe und Form:SolidMolekulargewicht:426.46Tivumecirnon
CAS:Tivumecirnon (FLX475) is a selective and oral CCR4 antagonist inhibits the infiltration and migration of Treg into the tumour microenvironment, antitumourFormel:C24H27Cl2F3N6OReinheit:99.88%Farbe und Form:SolidMolekulargewicht:543.41Plasiatine
CAS:Plasiatine is a novel potent activator of the nonreceptor protein tyrosine phosphatase shp2Formel:C20H18N2O6Farbe und Form:SolidMolekulargewicht:382.37Paltusotine HCl
CAS:Paltusotine, also known as CRN00808, is a somatostatin receptor agonist.Formel:C27H24Cl2F2N4OFarbe und Form:SolidMolekulargewicht:529.41YKL-05-093
CAS:<p>YKL-05-093 is a alt inducible kinase (SIK) inhibitor. YKL-05-093 increases bone formation and bone mass.</p>Formel:C35H40N6O4Farbe und Form:SolidMolekulargewicht:608.73NB-506 glucuronide
CAS:<p>NB-506 glucuronide is an indolocarbazole antitumor agent; a DNA topoisomerase I inhibitor.</p>Formel:C33H30N4O16Farbe und Form:SolidMolekulargewicht:738.61RK-582
CAS:RK-582: oral spiroindolinone tankyrase inhibitor, halts colon cancer growth in COLO-320DM mouse model.Formel:C27H35FN6O3Farbe und Form:SolidMolekulargewicht:510.6SirReal2
CAS:<p>SirReal2 is a potent and selective Sirt2 inhibitor with IC50 of 140 nM.</p>Formel:C22H20N4OS2Reinheit:98.96% - 99.75%Farbe und Form:SolidMolekulargewicht:420.55MX106
CAS:MX106 is a survivin inhibitor which induces degradation of XIAP and/or cIAP1, and suppresses genotoxic NF-kappaB activation.Formel:C25H30N2O2Farbe und Form:SolidMolekulargewicht:390.52GC813 sodium
CAS:GC813 is a potent and permeable inhibitor of MERS coronavirus 3CL protease. GC813 is analogue of GC376.Formel:C22H31ClN3NaO8SFarbe und Form:SolidMolekulargewicht:556DB2313 HCl
CAS:DB2313: first-in-class, potent inhibitor of PU.1, disrupts gene interactions, down-regulates PU.1 targets.Formel:C42H45Cl4FN8O2Farbe und Form:SolidMolekulargewicht:854.67MTR-105
CAS:<p>MTR-105 is a nitric oxide synthase inhibitor.</p>Formel:C7H19N2O4PSFarbe und Form:SolidMolekulargewicht:258.2728NLX-219
CAS:NLX-219 is a selective 5-HT1A receptor-biased agonists.Formel:C21H23ClF2N2O2Farbe und Form:SolidMolekulargewicht:408.87MX107
CAS:MX107 is a survivin inhibitor which induces degradation of XIAP and/or cIAP1, and suppresses genotoxic NF-kappaB activation.Formel:C24H28N2O2Farbe und Form:SolidMolekulargewicht:376.49VTP50469 mesylate
CAS:VTP-50469: oral MeninMLL1 inhibitor for MLL/NPM1c+ leukemia; kills affected cell lines.Formel:C33H51FN6O7S2Farbe und Form:SolidMolekulargewicht:726.9244O-1057 free base
CAS:O-1057 free base is a water-soluble cannabinoid receptor agonist with antinociceptive properties. RESEARCH USE ONLY.Formel:C32H46N2O4Farbe und Form:SolidMolekulargewicht:522.72O-1057 hydrochloride
CAS:<p>O-1057 hydrochloride is a water-soluble cannabinoid receptor agonist with antinociceptive properties. RESEARCH USE ONLY.</p>Formel:C32H47ClN2O4Farbe und Form:SolidMolekulargewicht:559.19Deptropine citrate
CAS:Deptropine citrate, an H1-histamine and muscarinic blocker, treats asthma and shows promise against breast cancer by reducing BCSCs viability.Formel:C29H35NO8Farbe und Form:SolidMolekulargewicht:525.59Benzo[a]pyrene
CAS:Benzo[a]pyrene (3,4-Benzopyrene) shows lung carcinogenicity in mice in a dose-dependent manner.Formel:C20H12Reinheit:98% - ≥98%Farbe und Form:Pale Yellow Monoclinic Needles From Benzene & Methanol Limits Its Spread To The Environment Easily Penetrates The Soil And Contaminates Groundwater OrMolekulargewicht:252.31SHR0687
CAS:<p>SHR0687: potent KOR agonist, selective, favorable PK, effective in rat pain model, minimal BBB penetration, less CNS side effects.</p>Formel:C39H60N8O5Farbe und Form:SolidMolekulargewicht:720.94Riminkefon
CAS:Riminkefon is a kappa opioid receptor agonist .Formel:C38H57N7O6Farbe und Form:SolidMolekulargewicht:707.9CS-003 HCl
CAS:CS-003 HCl is a TNRA - triple neurokinin receptor antagonist.Formel:C34H39Cl3N2O6SFarbe und Form:SolidMolekulargewicht:710.1AR-C117977
CAS:AR-C117977: Potent MCT1 inhibitor, reduces immune response, extends graft survival, induces tolerance in vitro/in vivo.Formel:C25H28N2O3S2Farbe und Form:SolidMolekulargewicht:468.63GD-131 hydrochloride
CAS:GD-131 hydrochloride is an inhibitor of extraneural uptake.Formel:C11H23Cl2NFarbe und Form:SolidMolekulargewicht:240.21USP25/28-IN-AZ2
CAS:USP25/28-IN-AZ2 is a novel potent, selective, dual usp25/28 inhibitorFormel:C17H17BrF3NO3Farbe und Form:SolidMolekulargewicht:420.22Pralurbactam
CAS:Pralurbactam is a β-Lactamase inhibitor utilized in the research of bacterial infections.Formel:C10H18N6O8SFarbe und Form:SolidMolekulargewicht:382.35DB293
CAS:DB293 inhibits PIT-1/BRN-3, binds as dimers in 5'-ATGA minor groove, expanding it.Formel:C19H16N6OFarbe und Form:SolidMolekulargewicht:344.37RTIOX-372
CAS:RTIOX-372 is a potent and selective orexin-1 receptor antagonist.Formel:C30H39N5O3Farbe und Form:SolidMolekulargewicht:517.66Obafistat Na
CAS:<p>Obafistat Na is an aldo-keto reductase AKR1C3 inhibitor.</p>Formel:C15H15FN5NaO3SFarbe und Form:SolidMolekulargewicht:387.37Sivelestat
CAS:<p>Sivelestat (ONO5046) is a potent and selective inhibitor of neutrophil elastase with IC50 of 44 nM.</p>Formel:C20H22N2O7SReinheit:98.34% - 99.54%Farbe und Form:SolidMolekulargewicht:434.46PSB-15160
CAS:<p>PSB-15160 is a compound that inhibits the growth of MCF7 (breast), NCI-H460 (lung) and SF-268 (NCS) cells in the treatment of estrogen-dependent tumours.</p>Formel:C17H12F2N2Reinheit:97.05%Farbe und Form:SolidMolekulargewicht:282.29Afeletecan HCl
CAS:Afeletecan (BAY 56-3722) is a water-soluble, anti-cancer camptothecin conjugated to a carbohydrate, inhibiting DNA replication and inducing apoptosis.Formel:C45H50ClN7O11SFarbe und Form:SolidMolekulargewicht:932.44Dihydrogenistein
CAS:Dihydrogenistein, derived from Genistein, inhibits tyrosine kinases and EGF receptor autophosphorylation.Formel:C15H12O5Farbe und Form:SolidMolekulargewicht:272.25CIDD-0067106
CAS:CIDD-0067106 is a novel potent and selective antiproliferative agent, inhibiting the activity of the mtorc1 pathwayFormel:C26H29N3O4Farbe und Form:SolidMolekulargewicht:447.53Mitapivat sulfate hydrate
CAS:Mitapivat sulfate hydrate (AG 348 sulfate hydrate) is a pyruvate kinase (PK) allosteric activator, used to study pyruvate kinase deficiency.Formel:C24H26N4O3S1H2SO43H2OReinheit:99.22%Farbe und Form:SolidMolekulargewicht:526.6photoGBI1
CAS:photoGBI1 is a photocontrol inhibitor of the voltage-gated proton channel Hv1.Formel:C16H18N8Farbe und Form:SolidMolekulargewicht:322.37BN80933
CAS:BN80933 is a dual inhibitor of lipid peroxidation and neuronal nitric oxide synthase; Neuroprotectant.Formel:C29H34N4O3SFarbe und Form:SolidMolekulargewicht:518.67ZIKV-IN-K22
CAS:ZIKV-IN-K22: antiviral against many coronaviruses, inhibits ZIKV replication, IC50 2.1 μM.Formel:C27H25BrN2O3Farbe und Form:SolidMolekulargewicht:505.4Cyanabactin
CAS:Cyanabactin is a novel ABA receptor agonist. It preferentially activates Pyrabactin Resistance 1 (PYR1) with low nanomolar potency.Formel:C18H18N2O2SFarbe und Form:SolidMolekulargewicht:326.41β-Chloro-L-alanine
CAS:β-Chloro-L-alanine (L-β-Chloroalanine), a bacteriostatic amino acid analog, inhibits a number of enzymes, including threonine deaminase and alanine racemase.Formel:C3H6ClNO2Reinheit:99.67%Farbe und Form:White Crystalline PowderMolekulargewicht:123.54ICRF-193
CAS:<p>ICRF-193 is a DNA topoisomerase II inhibitor.</p>Formel:C12H18N4O4Farbe und Form:SolidMolekulargewicht:282.3ICRF-196
CAS:ICRF-196 is a Topoisomerase II Inhibitor and antineoplastic agent.Formel:C12H18N4O4Farbe und Form:SolidMolekulargewicht:282.3TM-9
CAS:TM-9, an Alzheimer's drug, strongly inhibits both ChE and MAO-B.Formel:C21H20N2O2Farbe und Form:SolidMolekulargewicht:332.4Cefdinir monohydrate
CAS:Cefdinir monohydrate is a semi-synthetic, beta-lactam antibiotic that inhibits bacterial cell wall synthesis by binding to PBPs.Formel:C14H15N5O6S2Farbe und Form:SolidMolekulargewicht:413.42LLS30
CAS:<p>LLS30 inhibits Gal-1, reduces its binding affinity, and may help treat advanced prostate cancer.</p>Formel:C34H33Cl4N5O3Farbe und Form:SolidMolekulargewicht:701.47ProMMP-9 inhibitor-3c
CAS:<p>ProMMP-9 inhibitor-3c hinders MMP-9 homodimers, blocks proMMP-9/α4β1 integrin/CD44 binding, and detaches EGFR.</p>Formel:C18H20FN3O2SFarbe und Form:SolidMolekulargewicht:361.43Alprenolol tartrate
CAS:Alprenolol tartrate is a 5-HT1A antagonist.Formel:C19H29NO8Farbe und Form:SolidMolekulargewicht:399.44SPOP-IN-6lc
CAS:<p>SPOP-IN-6lc is a SPOP inhibitor with oncogenic effects in renal cancer cells.SPOP-IN-6lc can be used to study apoptosis.</p>Formel:C26H31N7O2SReinheit:99.19%Farbe und Form:SolidMolekulargewicht:505.64AA9 TG2 inhibitor
CAS:<p>AA9 is a novel transglutaminase (TG2) inhibitor.</p>Formel:C32H36N4O5Farbe und Form:SolidMolekulargewicht:556.65Bavarostat
CAS:Bavarostat: brain-penetrant HDAC6 inhibitor; IC50=60nM; >80x selective for HDAC6; modulates tubulin over histone acetylation.Formel:C20H27FN2O2Farbe und Form:SolidMolekulargewicht:346.44SKF 38393 hydrochloride
CAS:<p>SKF 38393 hydrochloride (SKF38393 HCl) is a selective dopamine D1/D5 receptor agonist.</p>Formel:C16H17NO2·HClReinheit:99.1% - 99.51%Farbe und Form:SolidMolekulargewicht:291.77YW1159
CAS:YW1159 is an inhibitor of Wnt signaling.Formel:C19H14FN5OFarbe und Form:SolidMolekulargewicht:347.35Pefabloc
CAS:Pefabloc: Irreversible inhibitor of serine proteases, blocks human/rat PAF-acetylhydrolase.Formel:C31H33N5O4S2Farbe und Form:SolidMolekulargewicht:603.75M133
CAS:M133 is a selective histone deacetylase HDAC1 and HDAC2 inhibitor and potent antitumor agent.Formel:C23H24N4OS2Farbe und Form:SolidMolekulargewicht:436.59M122
CAS:<p>M122 is a selective histone deacetylase HDAC1 and HDAC2 inhibitor and potent antitumor agent.</p>Formel:C24H25N5OS2Farbe und Form:SolidMolekulargewicht:463.62RK-52
CAS:RK-52: synthetic rhodesain inhibitor; ksecond = 67M min^-1, Ki = 38 pM, high affinity for trypanosomal protease.Formel:C30H32N2O4Farbe und Form:SolidMolekulargewicht:484.59FE-200041
CAS:FE-200041 is a peripheral efficacious kappa opioid agonist.Formel:C30H44N8O4Farbe und Form:SolidMolekulargewicht:580.72Fmoc-9-aminononanoic acid
CAS:<p>Fmoc-9-aminononanoic acid, used in PROTAC synthesis, has a terminal Fmoc-amine and carboxyl group, deprotects under basic conditions for conjugation.</p>Formel:C24H29NO4Farbe und Form:SolidMolekulargewicht:395.49SB02024
CAS:SB02024 inhibits VPS34, boosts cGAS-STING, hinders autophagy, and shrinks breast cancer xenografts; enhances Sunitinib/Erlotinib efficacy.Formel:C16H22F3N3O2Farbe und Form:SolidMolekulargewicht:345.36JBP485
CAS:JBP485 is an inhibitor of renal transporters OAT1 and OAT3. JBP485 is an antihepatitis agent as a substrate for intestinal PEPT1.Formel:C8H12N2O4Farbe und Form:SolidMolekulargewicht:200.19SKL2001
CAS:SKL2001, an agonist of the Wnt/β-catenin pathway, can disrupt the Axin/β-catenin interaction.Formel:C14H14N4O3Reinheit:97.46% - 99.99%Farbe und Form:SolidMolekulargewicht:286.29PS-519
CAS:PS-519 is a human tissue plasminogen activator and proteasome inhibitor.Formel:C12H19NO4Farbe und Form:SolidMolekulargewicht:241.28CGP 40215
CAS:<p>CGP 40215 is a specific S-adenosylmethionine decarboxylase (AdoMetDC) inhibitor that was found to inhibit the growth of Leishmania donovani promastigotes</p>Formel:C17H19N9Farbe und Form:SolidMolekulargewicht:349.39NSC-8891
CAS:<p>NSC-8891 is a Tyrosyl-DNA phosphodiesterase (Tdp1) inhibitor.</p>Formel:C27H33BrO5SFarbe und Form:SolidMolekulargewicht:549.52NSC109131
CAS:NSC109131 is an inhibitor of human tyrosyl-DNA phosphodiesterase 1 (TDP1).Formel:C27H34N4O2SFarbe und Form:SolidMolekulargewicht:478.65MAP3K14-IN-173
CAS:MAP3K14-IN-173 is a potent MAP3K14 kinase inhibitor.Formel:C29H31N7O2Farbe und Form:SolidMolekulargewicht:509.60Lonaprisan
CAS:<p>Lonaprisan: an oral steroid derivative with potent, selective anti-progestogenic effects, unaffected by PKA activators, active on PR-A/B.</p>Formel:C28H29F5O3Farbe und Form:SolidMolekulargewicht:508.52Sabarubicin
CAS:Sabarubicin: a doxorubicin analogue with potent antitumor effects; superior in DNA fragmentation and topoisomerase II poisoning.Formel:C32H37NO13Farbe und Form:SolidMolekulargewicht:643.64MC-70 hydrochloride
CAS:MC-70 hydrochloride inhibits P-gp and BCRP strongly (EC50: Caco-2 0.05μM, MDR1 0.69μM, MRP1 9.3μM, BCRP 73μM).Formel:C24H26ClNO3Farbe und Form:SolidMolekulargewicht:411.926NG25 trihydrochloride
CAS:NG25 trihydrochloride: kinase inhibitor for MAP4K2, TAK1, Src, LYN, Abl, CSK, FER, p38α; blocks TNF-α signals; impedes IFN secretion; anti-cancer properties.Formel:C29H33Cl3F3N5O2Farbe und Form:SolidMolekulargewicht:646.96WOBE437
CAS:WOBE437 is a selective endocannabinoid reuptake inhibitor which reduces disease progression in a mouse model of multiple sclerosisFormel:C22H33NO3Farbe und Form:SolidMolekulargewicht:359.5
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