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RepSox (E-616452) | TGF-beta/Smad Inhibitor | CAS 446859-33-2 | Selleck Chemicals
RepSox is a potent and selective inhibitor of the TGFβR-1/ALK5 with IC50 of 23 nM and 4 nM for ATP binding to ALK5 and ALK5 autophosphorylation in cel......
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CHIR-99021 (Laduviglusib) | GSK-3 Inhibitor | WNT Activator | CAS 252917-06-9 | Selleck Chemicals
GSK-3 inhibitor, IC50= 7 nM Find all the information about CHIR-99021 (CT99021) for cell signaling research.
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Laduviglusib (CHIR-99021) Hydrochloride | GSK-3 Inhibitor | WNT Activator | CAS 1797989-42-4 |...
GSK-3 inhibitor, IC50= 7 nM Find all the information about CHIR-99021 (CT99021) HCl for cell signaling research.
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Z-VAD-FMK | Caspase Inhibitor | CAS 187389-52-2 | Selleck Chemicals
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Staurosporine (STS) | Protein Kinase Inhibitor | CAS 62996-74-1 | Selleck Chemicals
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LEE011 (Ribociclib) | CDK4/6 Inhibitor | CAS 1211441-98-3 | Selleck Chemicals
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Bafilomycin A1 (Baf-A1) | V-ATPase Inhibitor | Autophagy Inhibitor | CAS 88899-55-2 | Selleck...
Bafilomycin A1 is a potent selective V-ATPase inhibitor and is a toxic macrolide antibiotic derived from Streptomyces griseus. Order Bafilomycin A1 from...
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BRUKINSA® (zanubrutinib) BTK Inhibitor | HCPs
Feb 20, 2026 - BRUKINSA® (zanubrutinib) is a BTKi indicated for adults with CLL/SLL, WM, MCL, MZL, and FL. See Important Safety Information and Prescribing Information.
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MG132 | Proteasome Inhibitor | CAS 1211877-36-9 | Selleck Chemicals
MG132 ((S,R,S)-(-)-MG-132, Z-Leu-D-Leu-Leu-al) is a potent proteasome(ChTL, TL, and PGPH)inhibitor. MG132 also inhibits calpain (IC50=1.2 μM). Quality...
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SB431542 | TGF-beta/Smad Inhibitor | Alk4/5 Inhibitor | CAS 301836-41-9 | Selleck Chemicals
SB-431542 is a potent and selective inhibitor of ALK5 with an IC50 of 94 nM. Find all the information about SB 431542 for cell signaling research.
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MRTX1133 is a highly selective inhibitor of mutant KRAS G12D and can reversibly binds to the activated and inactivated KRAS G12D mutants... Quality confirmed...
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RMC-7977 is a potent, reversible, tri-complex oral inhibitor that selectively targets active (GTP-bound) forms of KRAS, HRAS, and NRAS, which exhibits......
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Y-27632 Dihydrochloride | ROCK Inhibitor | CAS 129830-38-2 | Selleck Chemicals
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PD0325901 is MEK inhibitor and non-competitive with ATP, Kiapp of 1 nM against activated MEK1 and MEK2. Find all the information about PD0325901 for cell...
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https://www.selleckchem.com/products/cx-5461-pidnarulex-rna-polymerase-i-inhibitor.html
CX-5461 (Pidnarulex) | RNA Polymerase I Inhibitor | CAS 1138549-36-6 | Selleck Chemicals
CX-5461 is a potent small-molecule rRNA synthesis inhibitor with an IC50 of 0.11 μM. Find all the information about CX-5461 for cell signaling research.
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Wnt-C59 (C59) | PORCN Inhibitor | CAS 1243243-89-1 | Selleck Chemicals
Wnt-C59 (C59) is a PORCN inhibitor for Wnt3A-mediated activation of a multimerized TCF-binding site driving luciferase with IC50 of 74 pM in HEK293 ce......
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EPZ-6438 (Tazemetostat) | EZH2 Inhibitor | CAS 1403254-99-8 | Selleck Chemicals
Tazemetostat (EPZ-6438, E7438) is a potent, and selective EZH2 inhibitor with Ki and IC50 of 2.5 nM and 11 nM in cell-free assays, exhibiting a 35-fol......
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https://advos.io/en/lixte-biotechnology-advances-precision-oncology-with-novel-pp2a-inhibitor-lb-100
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Apr 27, 2026 - LIXTE Biotechnology is developing LB-100, a first-in-class PP2A inhibitor that enhances chemotherapy and radiation efficacy while reducing side effects, with...
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https://www.flapinhibitor.com/2019/05/02/7617/
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Protex Inhibitor
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https://www.irakinhibitor.com/2025/04/18/anti-dll4-antibody-abbott/
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Apr 18, 2025 - Product Name : DLL4Target points: AbbottStatus: Organization : ProteinShort name : Homo sapiensType: Organism: Antibodies are immunoglobulins secreted by...
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https://www.biospace.com/ascentage-pharma-s-mdm2-p53-inhibitor-apg-115-alrizomadlin-granted-an-orphan-drug-designation-by-the-fda-for-the-treatment-of-stage-iib-iv-melanoma-marking-the-twelfth-obtained-by-the-company
Ascentage Pharma's MDM2-p53 Inhibitor APG-115 (Alrizomadlin) Granted an Orphan Drug Designation by...
Jul 21, 2021 - Ascentage Pharma, a globally focused biotechnology company engaged in developing novel therapies for cancers, chronic hepatitis B, and age-related diseases,...
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AMPK Inhibitor
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https://www.rcsb.org/structure/7LT0
RCSB PDB - 7LT0: Hsp90a N-terminal inhibitor
Hsp90a N-terminal inhibitor
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Oct 14, 2025 - Name : FLJ43692 (Human) Recombinant Protein (P01)Biological Activity : Human FLJ43692 full-length ORF (BAC86243.1, 1 a.a. - 484 a.a.) recombinant protein with...
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https://www.selleck.be/nl-BE/products/tubastatin-a-hcl.html
Tubastatin A Hydrochloride | HDAC Remmer | HDAC Inhibitor | Op voorraad in België | Selleck België
Tubastatin A HCl is een potente en selectieve HDAC6-remmer met een IC50 van 15 nM in een celvrije test. Het is selectief (1000-voudig meer) tegenover alle...
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Olitigaltin (TD139) | Galectin-3 Inhibitor | Stock en España | Selleck España
Olitigaltin (TD-139, GB0-139) es un potente y selectivo inhibidor de galectin-3 con un Kd de 0,036 µM sobre galectin-1 y galectin-7 con un Kd de 2,2 µM y 32...
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https://arupconsult.com/ati/plasminogen-activator-inhibitor-1-serpine1-genotyping
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Supplementary test information for Plasminogen Activator Inhibitor-1 (SERPINE1) Genotyping such as test interpretation, additional tests to consider, and other...
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https://phekb.org/node/90/dictionaries
ACE Inhibitor (ACE-I) induced cough | PheKB
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https://stemwireoklahoma.com/article/910796111-pathos-ai-acquires-majority-stake-in-deuteroncology-to-advance-next-generation-met-inhibitor-identified-by-pathos-foundry-platform
Pathos AI Acquires Majority Stake in DeuterOncology to Advance Next-Generation MET Inhibitor...
https://www.globaltechnewspalestine.com/article/910796111-pathos-ai-acquires-majority-stake-in-deuteroncology-to-advance-next-generation-met-inhibitor-identified-by-pathos-foundry-platform
Pathos AI Acquires Majority Stake in DeuterOncology to Advance Next-Generation MET Inhibitor...
https://www.rcsb.org/structure/6KZN
RCSB PDB - 6KZN: Crystal Structure Of VIM-2 Metallo-beta-lactamase In Complex With Inhibitor X2
Crystal Structure Of VIM-2 Metallo-beta-lactamase In Complex With Inhibitor X2
https://www.mrtx-1133.com/
Inhibitor Insights Library – Inhibitor Research Hub
Curated inhibitor research articles, news, and expert resources covering the latest discoveries.
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https://www.tubulininhibitor.com/2025/11/26/gdf6-human-recombinant-protein/
GDF6 (Human) Recombinant Protein | Tubulin Inhibitor -tubulininhibitor.com
Nov 26, 2025 - Name : GDF6 (Human) Recombinant ProteinBiological Activity : Human GDF6 recombinant protein with polyhistidine tag at the C-terminus expressed in Escherichia...
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May 26, 2025 - Product Name : septin 2Target gene : SEPTIN2verified_species_reactivity : Humaninterspecies_information : 50%, ENSMUSG00000026276, species_id: MOUSE, 39%,...
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https://scholar.usuhs.edu/en/publications/the-orally-active-and-bioavailable-atr-kinase-inhibitor-azd6738-p/
The orally active and bioavailable ATR kinase inhibitor AZD6738 potentiates the anti-tumor effects...
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glucose-6-phosphatase, catalytic subunit | Ack1 Inhibitor
Jul 30, 2025 - Product Name : glucose-6-phosphatase, catalytic subunitTarget gene : G6PCverified_species_reactivity : Humaninterspecies_information : 94%, ENSMUSG00000078650,...
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BIX 02189, selective MEK5 inhibitor | Sano Bioscience
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https://www.mgmtinhibitor.com/2023/01/09/12345/
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corrosion inhibitor - HVAC Insider
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https://www.ghsrinhibitor.com/2023/12/18/11879/
Nce of iodide, Lys73 is not carboxylated and it adopts aNce of iodide, Lys73 is | GHSR Inhibitor...
Dec 18, 2023 - Nce of iodide, Lys73 is not carboxylated and it adopts aNce of iodide, Lys73 is just not carboxylated and it adopts a conformation in which its side chain...
https://xagena.it/news/medicinenews_net_farmaci/1b285431b6d97f0b3d25c629171a4448.html
Tomivosertib added on to continued checkpoint inhibitor therapy - Xagena
Despite the broad activity of checkpoint inhibitors across tumor types, primary or secondary resistance after initial response represents a major ...
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https://www.selleck.kr/products/exarafenib.html
Exarafenib (KIN-2787) | RAF Inhibitor | 국내 재고 보유 | Selleck 한국 (Selleck Korea)
Exarafenib (KIN-2787) 는 Raf 억제제. CAS 번호:2639957-39-2. 99.10% 순도. 재고 보유. 무료 분주 제공. ₩945,000 이상 구매 시 배송비 무료.
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https://www.ncbi.nlm.nih.gov/Structure/pdb/7SH9
7SH9: Structure of the SARS-CoV-2 main protease in complex with inhibitor MPI86
3C-like proteinase nsp5benzyl...
https://www.selleck.co.uk/products/abemaciclib-cdk4-6-inhibitor.html
Abemaciclib (LY2835219) | CDK4/6 inhibitor | UK Stock | Selleck UK
Abemaciclib (LY2835219) is a CDK Inhibitor. 128 citations, 99.97% purity. In stock. Free aliquoting. Free shipping over £409.
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https://www.cancernetwork.com/view/treatment-combo-egfr-inhibitor-resistant-lung-cancer
Treatment Combo for EGFR Inhibitor-Resistant Lung Cancer | CancerNetwork
May 11, 2026 - Combining the EGFR inhibitors afatinib and cetuximab resulted in clinical responses among advanced lung cancer patients who had previously stopped responding...
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https://www.hiv-protease.com/2025/12/31/sars-cov-2-b-1-1-529-omicron-spike-s1-protein-his/
SARS-CoV-2 B.1.1.529 (Omicron) Spike S1 Protein (His) | HIV Protease inhibitor hiv-protease.com
Dec 31, 2025 - Name : SARS-CoV-2 B.1.1.529 (Omicron) Spike S1 Protein (His)Description : The spike (S) glycoprotein of coronaviruses contains protrusions that will only bind...
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E pooled. Means SD are provided [n = 9 (day 0 and eight), n = | HAT Inhibitor hatinhibitor.com
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OTUB2 Protein | IRAK inhibitor-irakinhibitor.com
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Integrase Strand Transfer Inhibitor Use and Cancer Incidence in a Large Cohort Setting - Amsterdam...
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https://pubmed.ncbi.nlm.nih.gov/22199405/
Design and synthesis of a potential SH2 domain inhibitor bearing a stereodiversified...
Synthesis of a potential Src family SH2 domain inhibitor incorporating a 1,4-cis-enediol scaffold is reported. The synthetic route offers straightforward and...
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https://www.selleck.co.jp/screening/covalent-inhibitor-library.html
Covalent Inhibitor Library/Listing for Screening (384 well)
767種類の共有結合阻害剤または共有結合反応基を持つ小分子化合物のコレクションです。
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IWP-2 | Wnt/beta-catenin Remmer | Wnt/beta-catenin Inhibitor | Op voorraad in Nederland | Selleck...
IWP-2 is een remmer van Wnt-verwerking en -secretie met een IC50 van 27 nM in een celvrije assay, selectieve blokkering van Porcn-gemedieerde...
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AZD7648 | DNA-PK Inibitore | DNA-PK Inhibitor | Disponibile in Italia | Selleck Italia
AZD7648 è un potente inibitore di DNA-PK con una IC50 di 0,6 nM in saggio biochimico e più di 100 volte selettivo contro 396 altre chinasi.
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https://edoc.mdc-berlin.de/id/eprint/22701/
Tyrosine kinase inhibitor-induced defects in DNA repair sensitize FLT3(ITD)-positive leukemia cells...
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Le Belzutifan (PT2977), un inhibiteur de HIF-2α oralement actif et sélectif, augmente la puissance et améliore le profil pharmacocinétique, offrant un...
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Effect of recombinant hirudin, a specific inhibitor of thrombin, on endotoxin-induced intravascular...
https://www.rcsb.org/structure/1WAW
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Deucravacitinib (BMS-986165) is a highly potent and selective allosteric inhibitor of Tyk2 with a Ki value of 0.02 nM for binding to the Tyk2 pseudokinase...
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https://www.morressier.com/o/event/62daeef3a6fd3a00196fa00a/article/630fcb5a7e215f5e7f3754ea
Process development of the COVID-19 oral protease Inhibitor PF-07321332 at unprecedented speed:...
Shortly after the COVID-19 pandemic was declared in March 2020 by the WHO, Pfizer initiated a multi-front approach to combat the virus, which inc |
https://www.hiv-protease.com/2025/05/18/anti-tshr-car-antibody-university-of-florida/
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https://www.selleck.co.uk/products/Vincristine-Sulfate.html
Vincristine (Leurocristine) Sulfate | Microtubule Polymerization Inhibitor | UK Stock | Selleck UK
Vincristine (Leurocristine) Sulfate is Antineoplastic and Immunosuppressive Antibiotics Inhibitor. 129 citations, 99.94% purity. In stock. Free aliquoting....
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RAD51 inhibitor -rad51inhibitor.com
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https://www.hilarispublisher.com/abstract/proteasome-inhibitor-bortezomib-a-doubleedged-sword-in-cancertherapy-31834.html
Proteasome Inhibitor Bortezomib: A Double-Edged Sword in Cancer Therapy | Abstract
A steady flow of reports suggests that proteasome inhibitor bortezomib promotes tumor cell death by degradation of key proteins. Therefore, bortezomib..
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https://www.mgmtinhibitor.com/2022/03/25/11037/
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https://www.clinicaltrialsarena.com/news/beigene-trial-tyk2-inhibitor/
BeiGene commences Phase I trial of TYK2 inhibitor BGB-23339
Jul 11, 2022 - BeiGene has dosed the first subject in a Phase I trial of BGB-23339 being developed to potentially treat multiple immune-mediated disorders.
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https://ecancer.org/en/video/3301-biomarker-for-parp-inhibitor-responsiveness-in-ovarian-cancer-patients
Biomarker for PARP inhibitor responsiveness in ovarian cancer patients - ecancer
Prof Swisher talks to ecancertv at the 26th EORTC-NCI-AACR Symposium about data from a phase II trial, ARIEL2, which aims to identify pat
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https://edoc.ub.uni-muenchen.de/14506/
Gezielte molekulare Therapie des Mantelzell-Lymphoms In vitro Wirksamkeit von mTOR-Inhibitor RAD001...
https://scholars.uky.edu/es/publications/influence-of-the-novel-urease-inhibitor-n-n-butyl-thiophosphoric-/fingerprints/
Influence of the novel urease inhibitor N-(n-butyl) thiophosphoric triamide on ruminant nitrogen...
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Pefloxacin - DNA Gyrase Inhibitor Antibiotic | APExBIO
Pefloxacin is a broad-spectrum antibacterial agent that inhibits DNA gyrase (topoisomerase) to study bacterial DNA replication in microbiology research from...
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https://www.selleck.de/products/hro761-wrn-inhibitor.html
HRO761 | WRN-Inhibitor | Auf Lager in Deutschland | Selleck Deutschland
HRO761 ist ein potenter, selektiver, allosterischer Inhibitor der Werner-Syndrom-RecQ-Helikase (WRN). Er bindet an der Grenzfläche der D1- und...
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https://www.tubulininhibitor.com/2025/09/10/recombinant-human-cd50-icam-3-protein-his-tag/
Recombinant Human CD50 / ICAM-3 Protein (His tag) | Tubulin Inhibitor -tubulininhibitor.com
Sep 10, 2025 - Product Name : Recombinant Human CD50 / ICAM-3 Protein (His tag)TargetID : P32942Source : HEK293 CellsGene Accession Number : 3385Peptide Sequence : Met 1-His...
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Protease Inhibitor Cocktail: Optimizing Protein Degradation
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https://www.dnmtinhibitor.com/2025/01/10/cynomolgus-rhesus-macaque-kir3dl2-cd158k-his-tag/
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https://researchportal.murdoch.edu.au/esploro/outputs/journalArticle/Tissue-factor-pathway-inhibitor-antigen-and/991005542469707891?institution=61MUN_INST&skipUsageReporting=true&recordUsage=false
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https://unifind.uniss.it/resource/item/216845?language=en-US
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https://pure.fujita-hu.ac.jp/en/publications/ubiquitin-activating-enzyme-e1-inhibitor-pyr-41-retards-sperm-enl/fingerprints/
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https://www.selleck.co.uk/products/ly294002-pi3k-inhibitor.html
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SB273005 ist ein potenter Integrin-Inhibitor mit einer Ki von 1,2 nM für den αvβ3-Rezeptor und 0,3 nM für den αvβ5-Rezeptor.
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https://revistas.udem.edu.co/index.php/ingenierias/en/article/view/1544/2009
View of Evaluation of extract of neem tree (Azadirachta indica) as inhibitor of corrosion in saline...
https://www.vegfrinhibitor.com/2019/04/23/11376/
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https://discovery.dundee.ac.uk/en/publications/phase-iii-trial-of-batimastat-a-matrix-metalloproteinase-inhibito/
Phase I/II trial of batimastat, a matrix metalloproteinase inhibitor, in patients with malignant...
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