IDO
L'indoleamine 2,3-dioxygénase (IDO) est une enzyme impliquée dans le catabolisme du tryptophane, conduisant à la production de kynurénine et d'autres métabolites. L'IDO joue un rôle dans la tolérance immunitaire et est souvent surexprimée dans le cancer et les maladies inflammatoires chroniques. Les inhibiteurs de l'IDO sont explorés comme agents immunothérapeutiques potentiels dans le cancer et les maladies auto-immunes. Chez CymitQuimica, nous fournissons des inhibiteurs de l'IDO pour soutenir vos recherches en immunologie, oncologie et régulation métabolique.
84 produits trouvés pour "IDO"
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GNF-PF-3777
CAS :<p>GNF-PF-3777 (8-Nitrotryptanthrin) (8-Nitrotryptanthrin) is a potent inhibitor of human indoleamine 2,3-dioxygenase 2 (hIDO2; Ki: 0.97 μM).</p>Formule :C15H7N3O4Degré de pureté :97.88%Couleur et forme :SolidMasse moléculaire :293.23LY3381916
CAS :<p>IDO1-IN-5 is a selective, potent and brain penetrated inhibitor of IDO1 activity, binds to apo-IDO1 lacking heme rather than mature heme-bound IDO1.</p>Formule :C23H25FN2O3Degré de pureté :99.3%Couleur et forme :SolidMasse moléculaire :396.45IDO-IN-13
CAS :<p>IDO-IN-13 (GS-4361) is a potent indoleamine 2,3-dioxygenase 1 (IDO1) inhibitor (EC50: 17 nM).</p>Formule :C26H17F3N4ODegré de pureté :99.29%Couleur et forme :SolidMasse moléculaire :458.43BMT-297376
CAS :<p>BMT-297376, the optimized Linrodostat, is a potent IDO1 inhibitor.</p>Formule :C23H29F2N3O3Couleur et forme :SolidMasse moléculaire :433.5IDO-IN-15
CAS :IDO-IN-15 is an IDO1 inhibitor ( IC 50 < 0.51 nM).Formule :C29H39N5O4Couleur et forme :SolidMasse moléculaire :521.662NLG802
CAS :<p>NLG802 is a prodrug of indoximod, an orally active indoleamine 2,3-dioxygenase (IDO) inhibitor.</p>Formule :C20H30ClN3O3Degré de pureté :99.61%Couleur et forme :SolidMasse moléculaire :395.92IDO1-IN-11
CAS :<p>IDO1-IN-11 is an IDO1 inhibitor with an IC 50 value of 0.6 nM.</p>Formule :C22H17ClFN3O3Couleur et forme :SolidMasse moléculaire :425.84IDO1-IN-7
CAS :IDO1-IN-7 is a potent IDO1 inhibitor with a 6.1 nM IC50 and immunomodulatory effects for cancer research.Formule :C22H19ClFN3O3Couleur et forme :SolidMasse moléculaire :427.86IDO1/TDO-IN-8
<p>IDO1/TDO-IN-8 (Compound CZ-17) is a dual IDO1 and TDO inhibitor capable of crossing the blood-brain barrier, with EC50 values of 0.33 μM and 1.78 μM, respectively. It modulates the kynurenine pathway of tryptophan metabolism, reducing the kynurenine/tryptophan ratio. IDO1/TDO-IN-8 has neuroprotective effects, alleviating motor dysfunction and improving depressive behavior, making it relevant for research into Parkinson's disease with comorbid depression.</p>Formule :C17H14N2SCouleur et forme :SolidMasse moléculaire :278.37PROTAC IDO1 Degrader-1
CAS :First potent PROTAC IDO1 degrader; links IDO1 to CRBN E3 ligase for UPS-induced degradation (DC50=2.84 μM), boosts H ER2 CAR-T cell efficacy.Formule :C40H53BrFN9O13Couleur et forme :SolidMasse moléculaire :966.816CAY10581
CAS :CAY10581, a derivative of pyranonaphthoquinone, serves as a highly specific and reversible uncompetitive inhibitor of IDO, demonstrating potency with an IC50Formule :C22H21NO4Couleur et forme :SolidMasse moléculaire :363.41XW-032
<p>XW-032 is an apo-IDO1 inhibitor with an IC50 of 21 nM. In the CT26 syngeneic mouse model, XW-032 demonstrates significant in vivo antitumor efficacy with a TGI of 63%, showing potential for cancer research applications.</p>Couleur et forme :Odour Solidhuman TDO2-IN-1
<p>Human TDO2-IN-1 (Cpd-2) is a potent inhibitor of human TDO2, with an IC50 of 14.8 nM. It plays a significant role in studies related to metabolism, inflammation, and tumor immune surveillance.</p>Formule :C30H36N4O5Couleur et forme :SolidMasse moléculaire :532.631NU227326
CAS :<p>NU227326 is a PROTAC degrader of indoleamine 2,3-dioxygenase 1 (IDO1) with a DC50 value of 4.5 nM. It effectively degrades IDO1 in U87 and GBM43 cells, with DC50 values of 7.1 nM and 11.8 nM, respectively. NU227326 exhibits favorable pharmacokinetic properties, with a plasma half-life of 5.7 hours and a brain tissue half-life of 11.8 hours. (Pink: ligand for target protein IDO1 ligand-1; Black: linker; Blue: ligand for E3 ligase Cereblon).</p>Formule :C53H61FN8O7Couleur et forme :SolidMasse moléculaire :941.099TDO-IN-2
TDO-IN-2 is an orally active TDO inhibitor with an IC50 of 1.25 μM. It exhibits antitumor activity in a Hepa1-6 liver cancer allograft mouse model. Additionally, TDO-IN-2 works synergistically with PD-1/PD-L1 inhibitor BMS-202, making it useful for studying tumor immune tolerance.Formule :C20H15N3O3Couleur et forme :SolidMasse moléculaire :345.11134β-Cembrenediol
CAS :β-Cembrenediol (β-CBT) is a natural product from tobacco plants that is found in cigarette smoke condensate.Formule :C20H34O2Couleur et forme :SolidMasse moléculaire :306.49IDO1-IN-23
<p>IDO1-IN-23 (compound 41) is a potent inhibitor of human indoleamine 2,3-dioxygenase 1 (IDO1), exhibiting an IC50 of 13 μM [1].</p>Degré de pureté :98%Couleur et forme :Odour SolidIDO1/TDO-IN-7
<p>IDO1/TDO-IN-7 (Compound 43b), an isochinoline derivative, functions as a potent dual inhibitor of IDO1/TDO with IC50 values of 0.31 μM and 0.08 μM, respectively. Demonstrating favorable pharmacokinetics and strong antitumor efficacy in the B16-F10 tumor model, this compound also exhibits low toxicity.</p>Couleur et forme :Odour SolidIDO1-IN-24
IDO1-IN-24 (compound 2c) inhibits the production of IDO1 during cell assays, with an IC50 value of 17 μM.Formule :C18H22N2O4Masse moléculaire :330.15796NU223612
CAS :<p>"NU223612 is a potent IDO1-degrading PROTAC with Kd 640 nM, binds CRBN at 290 nM, and crosses the BBB."</p>Formule :C49H55FN6O9Couleur et forme :SolidMasse moléculaire :890.99IDO1-IN-12
CAS :IDO1-IN-12 is a potent and orally available IDO1 inhibitor.Formule :C21H19F3N2O2Couleur et forme :SolidMasse moléculaire :388.39IDO1/TDO-IN-4
CAS :<p>IDO1/TDO-IN-4 is a novel dual inhibitor of IDO1/TDO with antidepressant activity, forming hydrogen bonds with IDO1 and π-π stacking interactions with TDO.</p>Formule :C14H10N4Degré de pureté :98.88%Couleur et forme :SolidMasse moléculaire :234.26IDO1 Protein, Mouse, Recombinant (His)
IDO Protein, Mouse, Recombinant (His) is expressed in E.Degré de pureté :≥ 90 % as determined by SDS-PAGE. - ≥ 90 % as determined by SDS-PAGE.Couleur et forme :Lyophilized PowderMasse moléculaire :46.47 kDa (predicted)(Rac)-IDO1-IN-5
CAS :(Rac)-IDO1-IN-5 is a racemic, potent IDO1 inhibitor; selective for apo-IDO1, it crosses the blood-brain barrier.Formule :C23H25FN2O3Couleur et forme :SolidMasse moléculaire :396.45IDO1 Protein, Human, Recombinant (His)
IDO Protein, Human, Recombinant (His) is expressed in E.Couleur et forme :Lyophilized PowderMasse moléculaire :46 kDa (predicted); 44 kDa (reducing conditions)(S)-IDO1-IN-5
CAS :(S)-IDO1-IN-5 is an active S-isomer of IDO1-IN-5. (S)-IDO1-IN-5 binds to IDOL(IC50 value less than 1.5 μΜ).Formule :C23H25FN2O3Couleur et forme :SolidMasse moléculaire :396.45Anti-IDO1 Antibody (9Y885)
Anti-IDO1 Antibody (9Y885) is an antibody targeting IDO1. Anti-IDO1 Antibody (9Y885) can be used in ELISA, IHC.Couleur et forme :Odour LiquidIDO1 Protein, Human, Recombinant
IDO Protein, Human, Recombinant is expressed in E. coli expression system. The predicted molecular weight is 45.2 kDa and the accession number is A0A348GSI3.Couleur et forme :Lyophilized PowderMasse moléculaire :45.2 kDa (predicted); 46 kDa (reducing conditions)BMS-986242
CAS :BMS-986242 is an orally active, potent and selective inhibitor of indoleamine-2,3-dioxygenase 1 (IDO1), and it can be used for the research of cancer.Formule :C24H24ClFN2ODegré de pureté :98.9%Couleur et forme :SolidMasse moléculaire :410.91Linrodostat
CAS :Linrodostat (BMS-986205) is a selective indoleamine 2, 3-dioxygenase 1 (IDO1) inhibitor.Formule :C24H24ClFN2ODegré de pureté :99.54% - 99.71%Couleur et forme :SolidMasse moléculaire :410.91(S)-Indoximod
CAS :(S)-Indoximod (L-Abrine) is an indoleamine-2,3-dioxygenase (IDO) inhibitor for cancer research.Formule :C12H14N2O2Degré de pureté :95.39%Couleur et forme :SolidMasse moléculaire :218.253-TYP
CAS :<p>3-TYP (3-(1H-1,2,3-triazol-4-yl) pyridine) is a selective SIRT3 inhibitor.</p>Formule :C7H6N4Degré de pureté :99.16% - >99.99%Couleur et forme :SolidMasse moléculaire :146.15Indoximod
CAS :<p>Indoximod (NLG-8189) is a methylated tryptophan that inhibits IDO to boost T cell function by preventing tryptophan depletion.</p>Formule :C12H14N2O2Degré de pureté :97.82% - 99.55%Couleur et forme :SolidMasse moléculaire :218.25IDO-IN-7
CAS :IDO-IN-7 (NLG-919 analogue) is a potent IDO (indoleamine-(2, 3)-dioxygenase) pathway inhibitor.Formule :C18H22N2ODegré de pureté :99.32% - 99.9%Couleur et forme :SolidMasse moléculaire :282.38Epacadostat
CAS :Epacadostat (INCB 024360) is an oral, potent and selective IDO1 inhibitor with IC50 value of 71.8 nM.Cost-effective and quality-assured.Formule :C11H13BrFN7O4SDegré de pureté :98% - >99.99%Couleur et forme :SolidMasse moléculaire :438.23IDO-IN-1
CAS :<p>IDO-IN-1: potent IDO inhibitor, IC50 of 59 nM (enzyme), 12 nM (HeLa cells).</p>Formule :C9H7BrFN5O2Degré de pureté :99.91%Couleur et forme :SolidMasse moléculaire :316.09Navoximod
CAS :Navoximod (GDC-0919) (NLG- 919, GDC-0919) is a potent indoleamine-(2,3)-dioxygenase (IDO) pathway inhibitor (Ki/EC50: 7 nM/75 nM).Formule :C18H21FN2O2Degré de pureté :99.37%Couleur et forme :SolidMasse moléculaire :316.37Linrodostat mesylate
CAS :Linrodostat (BMS-986205) is an oral IDO1 inhibitor that boosts immune response and has anti-cancer properties.Formule :C25H28ClFN2O4SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :507.02IDO1-IN-1
CAS :IDO1-IN-1 (2 HzBTZ) is an indoleamine 2,3-dioxygenase 1 (IDO1) inhibitor.Formule :C7H7N3SDegré de pureté :99.36%Couleur et forme :Slightly Yellow To Beige-Green Crystalline PowderMasse moléculaire :165.22LM10
CAS :TDO inhibitor; IC50: human 0.62 μM, mouse 2 μM; selective over IDO, MAOs; hinders TDO+ tumor growth in mice; orally active.Formule :C11H8FN5Degré de pureté :98.78% - 99.94%Couleur et forme :SolidMasse moléculaire :229.21PCC0208009
CAS :PCC0208009 (IDO-IN-2) is an IDO inhibitor.Formule :C29H35N7ODegré de pureté :99.89%Couleur et forme :SolidMasse moléculaire :497.63IDO5L
CAS :IDO5L (INCB024360 analogue) is an effective IDO1 inhibitor(IC50=10 nM).Formule :C9H7ClFN5O2Degré de pureté :99.49% - 99.75%Couleur et forme :SolidMasse moléculaire :271.64PF-06840003
CAS :PF-06840003 (EOS200271) is a specific and oral active IDO-1 inhibitor.Formule :C12H9FN2O2Degré de pureté :99.10%Couleur et forme :SolidMasse moléculaire :232.21Necrostatin 2 racemate
CAS :<p>Necrostatin 2 racemate (Necrostatin-2 racemate) is an potent and specific inhibitor of RIPK1.</p>Formule :C13H12ClN3O2Degré de pureté :98% - 99.5%Couleur et forme :SolidMasse moléculaire :277.71DP00477
CAS :DP00477, a potent inhibitor of indoleamine 2,3-dioxygenase 1 (IDO1), exhibits an inhibitory concentration (IC50) of 7.0 µM.Formule :C17H11ClF3N3OSCouleur et forme :SolidMasse moléculaire :397.8IDO-IN-12
CAS :IDO-IN-12 is an inhibitor of indoleamine 2,3-dioxygenase (IDO).Formule :C13H11BrFN5O3SDegré de pureté :99.727%Couleur et forme :SolidMasse moléculaire :416.23IACS-8968 S-enantiomer
CAS :IACS-8968 S-enantiomer is the S-enantiomer of IACS-8968. IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO).Formule :C17H18F3N5O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :381.35IACS-8968
CAS :IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO).Formule :C17H18F3N5O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :381.35IDO1-IN-18
CAS :IDO1-IN-18 (Compound 14) is a potent inhibitor of IDO1. IDO1-IN-18 has potential for cancer disease research.Formule :C23H18F4N2O3Couleur et forme :SolidMasse moléculaire :446.39IDO-IN-8
CAS :IDO-IN-8 is an indoleamine 2,3-dioxygenase (IDO) inhibitor (IC50: 1-10 μM).Formule :C18H21FN2O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :316.37IDO-IN-6
CAS :IDO-IN-6 is an indoleamine 2,3-dioxygenase (IDO) inhibitor.Formule :C18H21FN2O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :316.37IDO1-IN-2
CAS :IDO1-IN-2 is a potent and selective IDO1 inhibitor with IC50s of 81 nM, 59 nM (mouse), and 28 nM (rat), respectively. It has anti-cancer activity.Formule :C15H17FN6O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :364.33IDO-IN-3
CAS :IDO-IN-3 is a potent indoleamine 2,3-dioxygenase (IDO) inhibitor (IC50: 290 nM).Formule :C11H12BrFN6O2Couleur et forme :SolidMasse moléculaire :359.15IDO-IN-11
CAS :<p>IDO-IN-11 is an indoleamine-2,3-dioxygenase (IDO) inhibitor with IC50s of 0.18 μM (Kinase) and 0.014 μM (Hela Cell).</p>Formule :C19H23BrFN7O4SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :544.4IDO1/TDO-IN-3
CAS :IDO1/TDO-IN-3 inhibits IDO1 (IC50: 0.005 μM) and TDO (IC50: 0.004 μM) with strong anti-tumor activity and low toxicity.Formule :C16H6ClF2N3O2Couleur et forme :SolidMasse moléculaire :345.69IDO-IN-4
CAS :IDO-IN-4 is an indoleamine 2,3-dioxygenase 1 (IDO-1) inhibitor.Formule :C26H35N3O3Couleur et forme :SolidMasse moléculaire :437.57IDO1-IN-16
CAS :IDO1-IN-16 (I-1) is an IDO1 inhibitor that targets holo-IDO1 (IC50: 127 nM).Formule :C25H35BrFN5O2Couleur et forme :SolidMasse moléculaire :536.48IACS-8968 R-enantiomer
CAS :IACS-8968 R-enantiomer is the R-enantiomer of IACS-8968. IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO).Formule :C17H18F3N5O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :381.35IDO1/TDO-IN-2
CAS :IDO1/TDO-IN-2: IDO1/TDO inhibitor; IC50s: IDO1, 0.1μM; TDO, 0.07μM; potential for cancer research.Formule :C16H9N3O2Couleur et forme :SolidMasse moléculaire :275.26IDO/TDO-IN-1
CAS :IDO/TDO-IN-1 is an orally active dual indoleamine-2,3-dioxygenase (IDO) and tryptophan 2,3-dioxygenase (TDO) inhibitor (IC50s: 9.7 and 47 nM).Formule :C25H24FN5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :413.49IDO1-IN-15
CAS :IDO1-IN-15 is an effective IDO1 inhibitor with IC50 of 127 nM. The potency of IDO1-IN-15 against IDO1 enzyme is comparable with Epacadostat in vitro.Formule :C13H14BrFN6O3Couleur et forme :SolidMasse moléculaire :401.19IDO-IN-16
CAS :IDO-IN-16 (compound 5) is an IDO inhibitor (IC50: 36 nM).Formule :C22H21F3N4OCouleur et forme :SolidMasse moléculaire :414.42IDO1-IN-17
CAS :IDO1-IN-17 (I-4) is an IDO1 inhibitor, with an IC 50 of 0.44 μM in hela cells .Formule :C28H32BrClFN5O2Couleur et forme :SolidMasse moléculaire :604.94IDO-IN-14
CAS :IDO-IN-14 is an IDO inhibitor (IC50: 0.6928 nM).Formule :C23H23ClN4O2Couleur et forme :SolidMasse moléculaire :422.91MMG-0358
CAS :MMG-0358 is a novel potent IDO1 inhibitor, showing low cytotoxicity and higher selectivity for IDO1 over TDO enzyme.Formule :C8H6ClN3OCouleur et forme :SolidMasse moléculaire :195.61IDO1-IN-21
CAS :IDO1-IN-21 (compound 10m), with an IC50 of 0.64 μM, acts as an IDO1 inhibitor and has demonstrated efficacy in suppressing tumor growth in murine models [1].Formule :C21H19F2N3O6SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :479.45IDO-IN-5
CAS :IDO-IN-5 is an indoleamine 2,3-dioxygenase (IDO) inhibitor (IC50: 1-10 μM).Formule :C18H21FN2O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :316.37Roxyl-9
CAS :Roxyl-9 is an inhibitor of IDO1 (Indoleamine 2,3-dioxygenase 1) [1].Formule :C18H13N3O2Couleur et forme :SolidMasse moléculaire :303.31TDO-IN-1
CAS :<p>TDO-IN-1 is a tryptophan 2,3-dioxygenase (TDO) inhibitor with antitumor activity that acts by reversing local immune tolerance in tumor tissues.</p>Formule :C16H13F3N4O2Degré de pureté :99.86%Couleur et forme :SolidMasse moléculaire :350.3IDO1/2-IN-1
CAS :First potent oral dual IDO1/IDO2 inhibitor with antitumor properties; IC50: 28 nM (IDO1), 144 nM (IDO2).Formule :C16H18BrFN8O4Couleur et forme :SolidMasse moléculaire :485.27(R)-IDO/TDO-IN-1
CAS :(R)-IDO/TDO-IN-1 (compound 25), an indoleamine-2,3-dioxygenase (IDO) inhibitor, demonstrates good pharmacokinetic properties and exerts anti-tumor effects in the MC38 xenograft model. This compound exhibits synergy when combined with the anti-PD-1 monoclonal antibody (SHR-1210) [1].Formule :C25H24FN5Couleur et forme :SolidMasse moléculaire :413.49NUCC-0223619
CAS :NUCC-0223619 is an IDO1 inhibitor that induces the degradation of IDO protein and can be involved in the synthesis of PROTAC.Formule :C24H24ClFN2O2Couleur et forme :SolidMasse moléculaire :426.91IDO1/2-IN-1 hydrochloride
CAS :IDO1/2-IN-1 hydrochloride: Dual IDO1/2 inhibitor, IC50 of 28/144 nM, oral, with antitumor properties.Formule :C16H19BrClFN8O4Couleur et forme :SolidMasse moléculaire :521.73IDO1/TDO-IN-6
CAS :IDO1/TDO-IN-6 (compound 11) is a dual inhibitor targeting IDO1 and TDO, exhibiting IC50 values of 2.25 μM for IDO1 and 2.89 μM for TDO.Formule :C20H17NO5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :351.35IDO-IN-9
CAS :IDO-IN-9 is an indoleamine-2,3-dioxygenase (IDO) inhibitor with IC50s of 0.011 μM (Kinase) and 0.0018 μM (Hela Cell).Formule :C13H13BrFN7O3SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :446.251-Isopropyltryptophan
CAS :1-Isopropyltryptophan (1-IsoPT), an IDO1 inhibitor, suppresses the expression of IDO-1 and IDO-2 mRNA induced by IFN-γ stimulation [1].Formule :C14H18N2O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :246.3IDO1 ligand-1
CAS :<p>IDO1ligand-1 is the target protein ligand for PROTAC NU227326, which is utilized for degrading IDO1.</p>Formule :C29H34FN3O2Couleur et forme :SolidMasse moléculaire :475.598IDO2-IN-1
CAS :<p>IDO2-IN-1: potent oral IDO2 inhibitor, IC50 = 112 nM, for inflammatory autoimmunity research.</p>Formule :C21H21BrN10O3Couleur et forme :SolidMasse moléculaire :541.36VS-15
CAS :VS-15 is a selective inhibitor of IDO1, specifically binding to its apo-heme form. Additionally, VS-15 serves as an inhibitor of iNOS.Formule :C29H27N5O3Couleur et forme :SolidMasse moléculaire :493.56IDO1-IN-13
IDO1-IN-13 is a potent IDO1 inhibitor (IC50: 61.6 nM, EC50: 30 nM in HeLa) that reduces kyn/trp ratio by 51% in SK-OV-3 tumors.Formule :C20H16BrN5O2SCouleur et forme :SolidMasse moléculaire :470.34IDO1-IN-25
CAS :<p>IDO1-IN-25, a dual inhibitor of IDO1/TDO2, showcases IC50 values of 0.17 μM for IDO1 and 3.2 μM for TDO2. It effectively suppresses NO production in RAW264.7 cells following stimulation with lipopolysaccharide (LPS). Additionally, IDO1-IN-25 demonstrates anti-inflammatory properties in a mouse ear edema model of acute inflammation induced by croton oil.</p>Formule :C14H8Cl3NO2SCouleur et forme :SolidMasse moléculaire :360.64IDO1-IN-14
IDO1-IN-14 is an IDO1 enzyme inhibitor with an IC50 of 396.9 nM and suppresses HeLa cell activity with an EC50 of 3393 nM.Formule :C18H12Cl2FN3O2Couleur et forme :SolidMasse moléculaire :392.21IDO antagonist-1
CAS :<p>IDO antagonist-1 (compound 163), an IDO antagonist, effectively inhibits the growth of pancreatic adenocarcinoma cells in C57BL/6 mice [1].</p>Formule :C39H53N7O5Couleur et forme :SolidMasse moléculaire :699.884-Phenyl-1H-1,2,3-triazole
CAS :<p>4-Phenyl-1H-1,2,3-triazole, an inhibitor of the enzyme IDO1 (IC50: 60 µM), is utilized in cancer research [1].</p>Formule :C8H7N3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :145.16
