Unter den Marken unserer mehr als 25 Partner sticht TargetMol hervor
We have reached an agreement with TargetMol: CymitQuimica clients will benefit for a 20% discount on all TargetMol products until the end of the year.On our website you can find the products offered by this partner, which has become one of the world's most recognised compound libraries and small molecule inhibitors supplier. TargetMol offers approximately 120 compound libraries and a wide range of chemical products and kits for life sciences.
Endet am 31. Dez.( 8 verbleibende Tage )
WUN 73823
CAS:WUN 73823 is a cyanine-PEG dye with excitation 649 nm/emission 667 nm, reactive carboxyl acid, used to form stable amides with amines.Formel:C37H47ClN2O10S2Farbe und Form:SolidMolekulargewicht:779.36VUN 00829
CAS:VUN 00829, a Cy5 labeled PEG with a reactive carboxyl end, enhances solubility and is trackable by its fluorescence.Formel:C45H65ClN2O10Farbe und Form:SolidMolekulargewicht:829.47SKOG102
CAS:SKOG102, a potent OLIG2 inhibitor, blocks DNA binding for GBM research.Formel:C19H25Cl2N7Farbe und Form:SolidMolekulargewicht:422.35Dihydronarwedine
CAS:Dihydronarwedine is a metabolite of Galanthamine, an inhibitor of glycogen synthase kinase 3β (GSK3β)Formel:C17H21NO3Farbe und Form:SolidMolekulargewicht:287.35Iferanserin HCl
CAS:Iferanserin HCl is a selective serotonin receptor antagonist.Formel:C23H29ClN2OFarbe und Form:SolidMolekulargewicht:384.95PEAQX sodium
CAS:<p>PEAQX (NVP-AAM077) is a competitive NMDA antagonist, mildly prefers GluN1/GluN2A to GluN2B, and acts as an anticonvulsant.</p>Formel:C17H15BrN3Na4O6PFarbe und Form:SolidMolekulargewicht:560.1588EML-405
CAS:<p>EML-405 is a small-molecule inhibitor of SPIN1 ( Kd of 14 uM).</p>Formel:C36H51N5O2Farbe und Form:SolidMolekulargewicht:585.82Pidnarulex HCl
CAS:Pidnarulex HCl is CX-5461, a selective Pol I inhibitor and p53 activator without DNA damage, showing potent anti-cancer efficacy.Formel:C27H28ClN7O2SFarbe und Form:SolidMolekulargewicht:550.08CAM4066
CAS:CAM4066 is a novel potent and selective CK2alpha inhibitor.Formel:C26H26ClN3O4Farbe und Form:SolidMolekulargewicht:479.96SNAP8 Acetate(868844-74-0,free base)
Diminishing the appearance of wrinkles.Formel:C43H74N16O18SReinheit:99.45%Farbe und Form:SolidMolekulargewicht:1135.21Nitroprusside disodium dihydrate
CAS:<p>Nitroprusside disodium dihydrate (Sodium Nitroprusside Dihydrate) is a potent vasodilator working through releasing NO spontaneously in blood.</p>Formel:C5H4FeN6Na2O3Reinheit:98%Farbe und Form:Bright RedMolekulargewicht:297.95EML631
CAS:EML631 is a potent and selective SPIN1 inhibitor (SPIN1 Kd= 3 microM).Formel:C41H60N6O3Farbe und Form:SolidMolekulargewicht:684.95CU-6PMN
CAS:CU-6PM, a fluorescent RXR agonist, allows easy rexinoid screening via fluorescence changes in microplate readers.Formel:C25H26O5Farbe und Form:SolidMolekulargewicht:406.47AS2541019
CAS:AS2541019 is a selective Phosphatidylinositol-3-kinase p110δ (PI3Kδ) inhibitor.Formel:C26H33F2N7O3Farbe und Form:SolidMolekulargewicht:529.58Lenumlostat
CAS:<p>Lenumlostat is a lysyl oxidase-like protein 2 (LOXL2) inhibitor with inhibitory effects on hLOXL2, hLOXL3 and LOXL2 for the study of fibrotic diseases.</p>Formel:C18H17F4N3O3Reinheit:99.11%Farbe und Form:SolidMolekulargewicht:399.34Variegatic acid
CAS:Variegatic acid inhibits β-hexosaminidase, TNF-α (IC50: 10.4, 16.8μM), and PKC β1 (IC50: 36.2μM) in RBL 2H3 cells.Formel:C18H12O9Farbe und Form:SolidMolekulargewicht:372.28GX-585
CAS:<p>GX-585 is a novel potent inhibitor of NaV1.7 and highly selective against NaV1.5, having limited selectivity against NaV1.1 and NaV1.2.</p>Formel:C24H25Cl2FN4O3SReinheit:99.02% - 99.03%Farbe und Form:SolidMolekulargewicht:539.45MDK3673
CAS:MDK3673, also known as Olfr895-Agonist-10, is a novel specific agonist of odorant receptor 895 (Olfr895).Formel:C14H17NO4Farbe und Form:SolidMolekulargewicht:263.29EphB1-IN-10
CAS:EphB1-IN-10 is a potent and selective covalent inhibitor of receptor tyrosine kinase EphB1.Formel:C17H15ClN4O2Farbe und Form:SolidMolekulargewicht:342.78Adriforant tartrate hydrate
CAS:<p>Adriforant (ZPL-3893787), a promising H4 receptor antagonist, may treat allergic diseases.</p>Formel:C17H32N6O8Farbe und Form:SolidMolekulargewicht:448.48Gougerotin
CAS:Gougerotin is an inhibitor of protein synthesis.Formel:C16H25N7O8Farbe und Form:SolidMolekulargewicht:443.41Sulfadiazine sodium
CAS:<p>Sulfadiazine sodium (Sulfadiazin-natrium) is a sodium salt form of sulfadiazine, an intermediate-acting bacteriostatic, synthetic sulfanilamide derivative.</p>Formel:C10H10N4O2S·NaReinheit:99.75%Farbe und Form:White To Off-White Crystalline PowderMolekulargewicht:272.26SAS-0132
CAS:SAS-0132 is a modulator/antagonist of sigma2R/TMEM97 and has potential for treating TBIs, Alzheimer's disease, and neuropathic pain.Formel:C24H29N3O2Farbe und Form:SolidMolekulargewicht:391.51BRF110
CAS:BRF110: brain-penetrant Nurr1:RXRα agonist, neuroprotective against PD, boosts dopamine, no dyskinesia in mice.Formel:C22H18F3N3O2Farbe und Form:SolidMolekulargewicht:413.39EPZ020411 HCl
CAS:EPZ020411: potent, selective PRMT6 inhibitor, good bioavailability in rats, enhances radiotherapy in GSC brain tumors.Formel:C25H40Cl2N4O3Farbe und Form:SolidMolekulargewicht:515.52Brigimadlin
CAS:Brigimadlin (BI 907828) is an orally active and highly potent antagonist of the E3 ubiquitin-protein ligase MDM2-p53 with antitumor activity.Formel:C31H25Cl2FN4O3Reinheit:98.17%Farbe und Form:SolidMolekulargewicht:591.46PSMA-1007
CAS:PSMA-1007 is a novel Glu-Ureido-type prostate-specific membrane antigen (PSMA) inhibitor.Formel:C49H55FN8O16Farbe und Form:SolidMolekulargewicht:1030.01NVR3-778 hydrate
CAS:<p>NVR 3-778: First CAM to show antiviral effects in HBV; 0.40 µM EC50; works across HBV genotypes, no cross-resistance with nucleoside inhibitors.</p>Formel:C18H18F4N2O5SFarbe und Form:SolidMolekulargewicht:450.4APHS
CAS:APHS is a cyclooxygenase-2 (COX-2) inhibitor with anti-inflammatory action. It also more potent than aspirin in the inhibition of COX-1.Formel:C15H18O2SFarbe und Form:SolidMolekulargewicht:262.37Fiduxosin hydrochloride
CAS:<p>Fiduxosin hydrochloride is an alpha 1a-adrenoceptor antagonist that may be useful in the treatment of Benign Prostatic Hyperplasia.</p>Formel:C30H30ClN5O4SFarbe und Form:SolidMolekulargewicht:592.11NAcM-COV
CAS:NAcM-COV is a specific, irreversible small molecule inhibitor targeting N-Acetyl-UBE2M interaction with DCN1 with IC50 of 28 nM.Formel:C28H35F3N4O2Farbe und Form:SolidMolekulargewicht:516.6Dichloro-all-trans-retinone
CAS:<p>Dichloro-all-trans-retinone is a selective inhibitor for retinaldehyde dehydrogenase enzymes, thereby irreversibly inhibiting RALDH1, 2, and 3.</p>Formel:C21H28Cl2OFarbe und Form:SolidMolekulargewicht:367.35Tauroursodeoxycholate sodium
CAS:Tauroursodeoxycholate sodium (TUDC) is an endoplasmic reticulum (ER) stress inhibitor, used for the treatment of gallstones and liver cirrhosis.Formel:C26H44NNaO6SReinheit:97.90%Farbe und Form:SolidMolekulargewicht:521.69LEO 134310
CAS:LEO 134310: Selective, non-steroidal GR agonist with 14 nM EC50, for topical skin disease treatment.Formel:C34H40N2O8Farbe und Form:SolidMolekulargewicht:604.69MFH290
CAS:MFH290 is a selective CDK12/13 inhibitor, covalently bonding with CDK12 Cys-1039, blocks Pol II CTD phosphorylation, and enhances olaparib's efficacy.Formel:C26H31N5O3S2Farbe und Form:SolidMolekulargewicht:525.69OAT-1441
CAS:<p>OAT-1441 is a hAMCase inhibitor.</p>Formel:C23H27ClN6OFarbe und Form:SolidMolekulargewicht:438.95VA4 TG2 inhibitor
CAS:VA4 is a novel irreversible TG2 transamidase site-specific inhibitor.Formel:C33H41N5O6SFarbe und Form:SolidMolekulargewicht:635.77Etoloxamine HCl
CAS:Etoloxamine HCl is the salt form of Etoloxamine free base, a histamine 1 receptor antagonist.Formel:C19H26ClNOFarbe und Form:SolidMolekulargewicht:319.87L0909
CAS:<p>L0909: Oral Hepatitis C inhibitor, novel action, EC50=0.022 μM, SI>600, blocks replication, effective against resistant strains.</p>Formel:C23H30ClN5Farbe und Form:SolidMolekulargewicht:411.97NK314
CAS:NK314, a benzo[c]phenanthridine, inhibits topoisomerase II causing DNA breaks within 1h, even without proteinase K digestion.Formel:C22H20ClNO4Farbe und Form:SolidMolekulargewicht:397.85INCB059872 tosylate
CAS:INCB059872: potent, selective oral LSD1 inhibitor, increasing tumor-suppressor gene expression by promoting H3K4 and H3K9 methylation.Formel:C37H50N2O9S2Farbe und Form:SolidMolekulargewicht:730.932Befiradol fumarate
CAS:Befiradol fumarate: potent 5-HT1A agonist for Parkinson's drug-induced dyskinesia.Formel:C24H26ClF2N3O5Farbe und Form:SolidMolekulargewicht:509.93Hexamethonium tartrate
CAS:Hexamethonium tartrate, a non-absorbable, brain-impenetrable ganglionic blocker, once used for hypertension, now a research tool.Formel:C20H38N2O122Farbe und Form:SolidMolekulargewicht:498.53SR12813
CAS:SR12813 (GW 485801) is a pregnane X receptor (PXR) agonist.Formel:C24H42O7P2Reinheit:99.43%Farbe und Form:SolidMolekulargewicht:504.53NCD38
CAS:NCD38 is a potent, selective LSD1 inhibitor.Formel:C37H37ClF3N3O4Reinheit:98.21% - 98.86%Farbe und Form:SolidMolekulargewicht:680.16CMX-521
CAS:CMX521: an antiviral for norovirus, effective against rotavirus; inhibits viral RNA polymerase.Formel:C13H17N5O5Reinheit:99.57%Farbe und Form:SolidMolekulargewicht:323.3CN-716 HCl
CAS:cn-716 is a novel Zika virus (ZIKV) NS2B-NS3pro protease inhibitor.Formel:C22H33BCl2N6O4Farbe und Form:SolidMolekulargewicht:527.25Citalopram oxalate
CAS:Citalopram oxalate: a serotonin uptake inhibitor, treats depression, lessens alcohol intake, favored for tardive dyskinesia over tricyclics.Formel:C22H23FN2O5Farbe und Form:SolidMolekulargewicht:414.43NLG802 HCl
CAS:NLG802, an oral indoximod prodrug, inhibits IDO enzyme, modulates immune response, and has anti-cancer properties.Formel:C18H26ClN3O3Farbe und Form:SolidMolekulargewicht:367.874MPT0L145
CAS:<p>MPT0L145 is a first-in-class PIK3C3/FGFR inhibitor.</p>Formel:C25H29Cl3N8O3Farbe und Form:SolidMolekulargewicht:595.91Ronopterin
CAS:Ronopterin is a potent Nitric oxide synthase inhibitor and Neuroprotectant.Formel:C9H16N6O2Farbe und Form:SolidMolekulargewicht:240.26SB1-F-78
CAS:SB1-F-78 is an USP30 inhibitor.Formel:C17H16N6OSFarbe und Form:SolidMolekulargewicht:352.41PF-06862309
CAS:PF-06862309 is a PI3K inhibitorFormel:C20H26F3N8O7PFarbe und Form:SolidMolekulargewicht:578.44CGP-78608
CAS:CGP-78608 is a glycine site-specific N-methyl-D-aspartate receptor antagonist prevents activation of the NMDA/NO/CGMP pathway by ammonia.Formel:C11H13BrN3O5PFarbe und Form:SolidMolekulargewicht:378.12Ochromycinone
CAS:<p>Ochromycinone (STA 21) is a selective STAT3 inhibitor.</p>Formel:C19H14O4Reinheit:99.21%Farbe und Form:SolidMolekulargewicht:306.31Delgocitinib EtOH
CAS:Delgocitinib (LEO-124249/JTE052) is a selective JAK inhibitor used for reducing skin inflammation and treating chronic dermatitis.Formel:C18H24N6O2Farbe und Form:SolidMolekulargewicht:356.43BiBET
CAS:BiBET is a potent, selective, bivalent inhibitor of BET bromodomains.Formel:C26H30N10O3Farbe und Form:SolidMolekulargewicht:530.58MK-8666 Tris
CAS:<p>MK-8666, a partial GPCR agonist, targets GPR40 to enhance insulin secretion, potentially treating type 2 diabetes without adverse effects.</p>Formel:C33H42N2O9SFarbe und Form:SolidMolekulargewicht:642.764Fasoracetam monohydrate
CAS:Fasoracetam monohydrate: synthetic, activates glutamate receptors, trialed in Phases I-III for vascular dementia.Formel:C11H21N3O5Farbe und Form:SolidMolekulargewicht:275.31JPI-547 HCl
CAS:JPI-547 (NOV 1402) is an oral anti-cancer drug targeting PARP 1/2 and Tankyrase 1/2, effective alone or with chemo and immunotherapies.Formel:C23H26Cl2N6OFarbe und Form:SolidMolekulargewicht:473.402KR30031
CAS:KR30031 is a novel verapamil-like P-glycoprotein inhibitor with fewer heart side-effects, potentially boosting paclitaxel's efficacy.Formel:C26H34N2O4Farbe und Form:SolidMolekulargewicht:438.56Quoromycin
CAS:Quoromycin, a new antivirulence drug, hinders Vibrio vulnificus by disrupting SmcR in quorum-sensing, reducing virulence in vitro and in vivo.Formel:C12H8N2O2SFarbe und Form:SolidMolekulargewicht:244.27Tofacitinib maleate
CAS:<p>Tofacitinib (tasocitinib, CP-690550) is a JAK inhibitor blocking cytokine signaling and STAT activation.</p>Formel:C16H20N6O·xC4H4O4Farbe und Form:SolidMolekulargewicht:428.449NAS-181 free base
CAS:NAS-181 free base is a 5-HT(1B) receptor antagonist.Formel:C19H26N2O4Farbe und Form:SolidMolekulargewicht:346.42SU 5402
CAS:SU 5402 is a potent multi-targeted receptor tyrosine kinase inhibitor with IC50 of 20 nM, 30 nM, and 510 nM for VEGFR2, FGFR1, and PDGF-Rβ, respectively.Formel:C17H16N2O3Reinheit:98.91% - 99.64%Farbe und Form:Yellow-Green SolidMolekulargewicht:296.32CJ-15161 hydrochloride
CAS:CJ-15161 hydrochloride is the salt form of CJ-15161 (free base), an opioid κ-receptor agonist, is undergoing development with Pfizer as an analgesic agent.Formel:C23H32ClN3O2Farbe und Form:SolidMolekulargewicht:417.978CJ-15161 (free base)
CAS:<p>CJ-15161 (free base), an opioid κ-receptor agonist, is undergoing development with Pfizer as an analgesic agent.</p>Formel:C23H31N3O2Farbe und Form:SolidMolekulargewicht:381.51IDN-1965
CAS:IDN-1965: potent, irreversible caspase inhibitor; blocks Fas-induced apoptosis; varied administration; promising for liver injury treatment.Formel:C21H26FN3O5Farbe und Form:SolidMolekulargewicht:419.45Bornaprine
CAS:Bornaprine is an anticholinergic drug used to treat Parkinson's disease due to inhibition of muscarinic or nicotinic transmission.Formel:C21H31NO2Farbe und Form:SolidMolekulargewicht:329.48TP1287
CAS:TP-1287 is an oral phosphate prodrug of the CDK9 inhibitor, alvocidib.Formel:C21H21ClNO8PFarbe und Form:SolidMolekulargewicht:481.82Laropiprant analog
CAS:Laropiprant analog is an antagonist of the prostaglandin PGD2 receptor DP1.Formel:C20H18ClFN2O4SFarbe und Form:SolidMolekulargewicht:436.88ML416
CAS:<p>ML416 is an inhibitor of HIV-1.</p>Formel:C14H15FN2OS2Farbe und Form:SolidMolekulargewicht:310.41RWJ-60475
CAS:RWJ-60475 is a novel CD45 phosphatase inhibitor.Formel:C13H11BrNO7PFarbe und Form:SolidMolekulargewicht:404.11SU6656
CAS:SU 6656 is a selective inhibitor of Src family kinases, with IC50 of 280 nM, 20 nM, 130 nM, and 170 nM for Src, Yes, Lyn, and Fyn, respectively.Formel:C19H21N3O3SReinheit:98.21% - 98.73%Farbe und Form:SolidMolekulargewicht:371.45AZD5718
CAS:AZD5718: potent FLAP inhibitor (IC50=2.0 nM), treats Coronary Artery Disease, >90% leukotriene suppression, safe in animal studies, in phase 2a trial.Formel:C29H34N6O4Farbe und Form:SolidMolekulargewicht:530.62GNF7156
CAS:GNF7156 is a potent and selective DYRK1A inhibitor.Formel:C22H22N6O3Farbe und Form:SolidMolekulargewicht:418.45ONL-1204
CAS:ONL-1204 is a small molecule, CD95 antigen inhibitor (Fas inhibitor) being developed by ONL Therapeutics for the treatment of retinal detachment.Formel:C71H100N18O16Farbe und Form:SolidMolekulargewicht:1461.66PF-04363467 HCl
CAS:<p>PF-04363467 HCl is a selective dopamine D3/D2 receptor antagonist.</p>Formel:C22H30N2O3SFarbe und Form:SolidMolekulargewicht:402.55Phenamil
CAS:Phenamil is an inhibitor of epithelial sodium channels, activates the osteomorphin protein pathway to promote bone repair and induces significant fat formation.Formel:C12H12ClN7OReinheit:99.07%Farbe und Form:SolidMolekulargewicht:305.72Istaroxime oxalate
CAS:<p>Istaroxime (PST-2744) is a positive inotrope that inhibits Na+/K+ ATPase, raising intracellular sodium and calcium levels.</p>Formel:C23H34N2O7Farbe und Form:SolidMolekulargewicht:450.53WS-691
CAS:<p>WS-691: potent oral ABCB1 modulator; lowers PTX IC50 to 22.02 nM in SW620/Ad300 cells; raises [3H]-PTX uptake; non-toxic in vivo.</p>Formel:C20H16FN7SFarbe und Form:SolidMolekulargewicht:405.45BC-1485
CAS:<p>BC-1485 is a small molecule inhibitor of FIEL1 that inhibits the degradation of PIAS4 and ameliorates fibrosis in a mouse model.</p>Formel:C19H21N5O5SReinheit:97.03% - 97.15%Farbe und Form:SolidMolekulargewicht:431.47Brostallicin HCl
CAS:Brostallicin, a synthetic MGB, inhibits DNA replication in cancer cells, inducing cell death, effective against MMR-defective tumors.Formel:C30H36BrClN12O5Farbe und Form:SolidMolekulargewicht:760.04Risvodetinib
CAS:Risvodetinib: potent inhibitor of protein tyrosine kinases c-Abl1, c-Abl2, and c-kit.Formel:C33H34N8O2Farbe und Form:SolidMolekulargewicht:574.68Tedizolid Phosphate
CAS:Tedizolid Phosphate (TR-701FA) is an oxazolidinone-class antibiotic. Tedizolid phosphate is a phosphate ester prodrug of the active compound tedizolid.Formel:C17H16FN6O6PReinheit:97.96%Farbe und Form:SolidMolekulargewicht:450.32XMU-MP-2
CAS:<p>XMU-MP-2 is a potent and selective protease inhibitor with anticancer activity that inhibits the growth of oncogenic BRK-driven tumors in a mouse xenograft</p>Formel:C32H33F3N8O2Reinheit:99.29%Farbe und Form:SolidMolekulargewicht:618.65CRM-51005
CAS:<p>CRM-51005 is a new phospholipase C inhibitor produced by unidentified fungal strain MT51005</p>Formel:C15H20O3Farbe und Form:SolidMolekulargewicht:248.32VPC-16606
CAS:VPC-16606 inhibits ERα cell growth & gene expression, blocking ERα-LBD & SRC-3 binding dose-dependently.Formel:C17H13ClN2O2SFarbe und Form:SolidMolekulargewicht:344.82Ixazomib citrate EtOH
CAS:Ixazomib citrate (MLN9708), a prodrug of Ixazomib, is an oral, next-gen proteasome inhibitor with enhanced anti-cancer properties.Formel:C22H29BCl2N2O10Farbe und Form:SolidMolekulargewicht:563.188Ticalopride
CAS:Ticalopride: 5-HT3 agonist for digestive, orofacial, ENT disorders, and bulimia, GERD, IBS research.Formel:C14H20ClN3O3Reinheit:99.51%Farbe und Form:SolidMolekulargewicht:313.78Lifirafenib HCl
CAS:Lifirafenib (Beigene-283/BGB-283): a potent, selective RAF/EGFR inhibitor effective against B-RAF mutated colorectal cancers.Formel:C26H19ClF3N3O3Farbe und Form:SolidMolekulargewicht:513.9012BMS-955176 HCl
CAS:<p>GSK-3532795: a broader-spectrum HIV-1 maturation inhibitor than bevirimat, effective in vitro and clinically.</p>Formel:C42H62N2O4SFarbe und Form:SolidMolekulargewicht:727.486AMG2504
CAS:AMG2504 is a TRPA1 inhibitor.Formel:C15H10Cl4N2O3SFarbe und Form:SolidMolekulargewicht:440.13Metitepine
CAS:Metitepine is a serotonin receptor antagonist in the CNS used as an antipsychotic.Formel:C20H24N2S2Farbe und Form:SolidMolekulargewicht:356.55(S)-Pomalidomide
CAS:(S)-Pomalidomide is an inhibitor of angiogenesis and growth of B-cell neoplasias, which induces complete regressions of Burkitt's lymphoma cell tumors.Formel:C13H11N3O4Farbe und Form:SolidMolekulargewicht:273.24Teneligliptin hydrobromide
CAS:Teneligliptin hydrobromide: potent, novel DPP-4 inhibitor; inhibits human/rat plasma DPP-4 with ~1 nM IC50.Formel:C22H30N6OSBrHReinheit:97.83% - 99.92%Farbe und Form:SolidMolekulargewicht:628.86Ruboxistaurin mesylate monohydrate
CAS:<p>Ruboxistaurin mesylate monohydrate, a PKC beta inhibitor, may treat diabetic nephropathy and macular edema, reducing oxidative stress and neovascularization.</p>Formel:C29H34N4O7SFarbe und Form:SolidMolekulargewicht:582.67Difenamizole HCl
CAS:Difenamizole HCl, a pyrazolone NSAID with analgesic effects, modulates dopamine and inhibits monoamine oxidase.Formel:C20H23ClN4OFarbe und Form:SolidMolekulargewicht:370.88Glutathione sodium
CAS:<p>Glutathione sodium, a water-soluble form of PAO, blocks blood vessel formation and cancer growth.</p>Formel:C10H16N3NaO6SFarbe und Form:SolidMolekulargewicht:329.3BIM-46068
CAS:<p>BIM-46068 is a potent inhibitor of human farnesyltransferase with a unique anti-proliferative profile.</p>Formel:C21H42N4O3S3Farbe und Form:SolidMolekulargewicht:494.78
