Our AI-powered biological discovery engine, BDE-Bio, combines massive scientific research literature, patent and comprehensive biological data of the targets / biomarkers related to specific diseases and generates customized review reports to facilitate your projects of life science research or pharmaceutical discovery and development.
Targets / Biomarkers in Diseases
AI-POWERED REVIEW REPORTS
Introduction
BDE-Bio achieves information about the disease targets of your interest by combining 24-hour continuously updated massive scientific research literature, comprehensive biological databases, and large-scale multi-omics data, and provides AI-powered customized comprehensive reports covering all aspects that you need, from basic biology to in vitro / in vivo experiments and to drugs on the market.
1) Capture: 24-hour monitoring of Pubmed, 24 public databases (genecard, drugbank, pubchem, etc.), real-time inbound parsing.
2) Extraction: Extracts basic information about the target, protein structure, biological mechanism of the target, drug resistance of the target, disease correlation, etc.
3) Analysis: Summarizes the contents and generates customized comprehensive reports.
Target Prediction
Predicting targets that can successfully enter the clinical trial stage and ensuring that lead compounds based on predicted targets can successfully break through the PCC stage within an estimated time frame.
Target-based Drug Prediction
Predicting the difficulty level of target-based drug development provides a basis for assessing the value of target exploration.
Disease-Related Target Prediction
Predicting key targets for specific diseases and provide a basis for drug development for rare diseases and difficult and complicated diseases.
Targets and Diseases
Common Targets
11beta-Hydroxysteroid Dehydrogenase | 14-3-3 Protein | 15-Lipoxygenase | 17-beta-Hydroxysteroid dehydrogenase | 28S ribosomal subunit, mitochondrial | 3-Ketoacyl-CoA Thiolase (3-KAT) | 39S ribosomal subunit, mitochondrial | 4EHP-GYF2 complex | 5-Hydroxytryptamine Receptor | 5-Hydroxytryptamine Receptor 1 (5-HT1) | 5-Hydroxytryptamine Receptor 2 (5-HT2) | 60S Ribosome | 9-1-1 cell-cycle checkpoint response complex | A-Kinase Anchor Proteins | A1BG | A1BG-AS1 | A1CF | A2M | A2M-AS1 | A2ML1 | A2MP1 | A3GALT2 | A4GALT | A4GNT | AAAS | AACS | AACSP1 | AADAC | AADACL2 | AADACL2-AS1 | AADACL3 | AADACL4 | AADACP1 | AADAT | AAGAB | AAK1 | AAMDC | AAMP | AANAT | AAR2 | AARD | AARS1 | AARS2 | AARSD1 | AASDH | AASDHPPT | AASS | AATBC | AATF | AATK | ABALON | ABAT | ABCA1 | ABCA10 | ABCA11P | ABCA12 | ABCA13 | ABCA17P | ABCA2 | ABCA3 | ABCA4 | ABCA5 | ABCA6 | ABCA7 | ABCA8 | ABCA9 | ABCB1 | ABCB10 | ABCB11 | ABCB4 | ABCB5 | ABCB6 | ABCB7 | ABCB8 | ABCB9 | ABCC1 | ABCC10 | ABCC11 | ABCC12 | ABCC13 | ABCC2 | ABCC3 | ABCC4 | ABCC5 | ABCC6 | ABCC6P1 | ABCC6P2 | ABCC8 | ABCC9 | ABCD1 | ABCD2 | ABCD3 | ABCD4 | ABCE1 | ABCF1 | ABCF1-DT | ABCF2 | ABCF3 | ABCG1 | ABCG2
Common Diseases
17-beta-hydroxysteroid Dehydrogenase X Deficiency | 3-hydroxy-3-methylglutaric Aciduria | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | 3-M Syndrome | 3-methylcrotonyl-CoA Carboxylase Deficiency | 3-methylglutaconic Aciduria | 3-methylglutaconic Aciduria Type I | 3-methylglutaconic Aciduria Type IV | 3C Syndrome | 5-oxoprolinase Deficiency | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Aarskog-Scott Syndrome | Abetalipoproteinemia | Absence Epilepsy | Acanthosis Nigricans | Aceruloplasminemia | Achondrogenesis | Achromatopsia | Acne | Acne Vulgaris | Acquired Partial Lipodystrophy | Acral Lentiginous Melanoma | Acrocallosal Syndrome | Acrodermatitis | Acrodermatitis Enteropathica | Acrodysostosis | Acromegaly | Acromesomelic Dysplasia | Acromicric Dysplasia | ACTH-independent Macronodular Adrenal Hyperplasia | Actinomycetoma | Acute Anterior Uveitis | Acute Chest Syndrome | Acute Coronary Syndrome | Acute Generalized Exanthematous Pustulosis | Acute Kidney Injury | Acute Leukemia | Acute Lung Injury | Acute Lymphocytic Leukemia | Acute Motor Axonal Neuropathy | Acute Myeloid Leukemia | Acute Tubular Necrosis | Adams-Oliver Syndrome | Addison Disease | Adenocarcinoma | Adenoid Cystic Carcinoma | Adenoma, Pituitary | Adenoma, Pleomorphic | Adenoma, Villous | Adenomatoid Tumor | Adenomyosis | Adenosine Deaminase 2 Deficiency | Adenosine Deaminase Deficiency | Adenylosuccinate Lyase Deficiency | ADNP Syndrome | Adrenal Insufficiency | Adrenoleukodystrophy, X-linked | Adrenomyeloneuropathy | Adult Polyglucosan Body Disease | Agammaglobulinemia | Agnathia-Otocephaly Complex | Agoraphobia | Agranulocytosis | Aicardi-Goutieres Syndrome | AIDS | AIDS Dementia Complex | Alagille Syndrome | Alazami Syndrome | Albinism | Alcoholism | Aldosterone Deficiency | Aldosterone Synthase Deficiency | Aldosteronism | Alexander Disease | Alkaptonuria | Allan-Herndon-Dudley Syndrome | Allergic Contact Dermatitis | Alopecia | Alopecia Areata | Alopecia Totalis | Alpers Syndrome | Alpha-1 Antitrypsin Deficiency | Alpha-mannosidosis | Alpha-thalassemia Myelodysplasia Syndrome | Alstrom Syndrome | Alveolar Capillary Dysplasia | Alzheimer Disease, Late Onset | Amblyopia | Amebiasis | Amelanotic Melanoma | Ameloblastic Carcinoma | Ameloblastoma | Amelogenesis Imperfecta | Amenorrhea | Amish Infantile Epilepsy Syndrome | Amyloidosis | Amyotrophic Lateral Sclerosis | Amyotrophic Lateral Sclerosis, Juvenile | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Anal Fissure | Analgesia | Androgen Insensitivity | Androgenic Alopecia | Anemia | Anencephaly | Aneurysm, Abdominal Aortic | Aneurysm, Thoracic Aortic | Angelman Syndrome | Angina Pectoris | Angiodysplasia | Angioedema | Angioedema, Acquired | Angioedema, Hereditary | Angioimmunoblastic T-cell Lymphoma | Angiomyolipoma | Angiosarcoma | Angiosarcoma Of The Breast | Anodontia | Anorchia | Anorectal Fistula | Anorectal Malformations | Anorexia Nervosa | Anosmia, Congenital | Anovulation | Antenatal Bartter Syndrome Type 1 | Anterior Segment Dysgenesis | Anthrax | Anti-glomerular Basement Membrane Disease | Anti-NMDA Receptor Encephalitis | Antiphospholipid Syndrome | Antisocial Personality Disorder | Antisynthetase Syndrome | Antithrombin III Deficiency | Antley-Bixler Syndrome | Anuria | Anxiety Disorders | Apert Syndrome | Aphasia | Aplasia Cutis Congenita | Aplastic Anemia | Apparent Mineralocorticoid Excess Syndrome | Apraxia | Argininosuccinic Aciduria | Aromatic L-amino Acid Decarboxylase Deficiency | Arrhythmogenic Right Ventricular Cardiomyopathy | Arterial Tortuosity Syndrome | Arteriosclerosis | Arteriovenous Malformations | Arthritis | Arthritis, Gouty | Arthritis, Psoriatic | Arthritis, Reactive | Arthrogryposis | Arthropathy | Arts Syndrome | Aspartylglycosaminuria | Asperger Syndrome | Aspergillosis | Asphyxia Neonatorum | Asplenia | Asthma | Asthma, Exercise-induced | Asthma, Nocturnal | Astigmatism | Astrocytoma | Astrocytoma, Anaplastic | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Ataxia-ocular Apraxia 2 | Atelosteogenesis Type 1 | Atelosteogenesis Type 2 | Atherosclerosis | Atopic Dermatitis | Atopy | Atrial Septal Defect | Atrioventricular Septal Defect | Auriculocondylar Syndrome | Autism | Autism Spectrum Disorders | Autoimmune Autonomic Ganglionopathy | Autoimmune Disease | Autoimmune Hemolytic Anemia | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Autoimmune Polyendocrine Syndrome | Autoimmune Polyendocrinopathy Syndrome Type I | Autonomic Nervous System Disorders | Autonomic Neuropathy | Autosomal Recessive Bestrophinopathy | Autosomal Recessive Congenital Ichthyosis | Autosomal Recessive Spastic Paraplegia Type 35 | Autosomal Recessive Spastic Paraplegia Type 54 | Autosomal Recessive Spastic Paraplegia Type 75 | Avellino Corneal Dystrophy | Avian Influenza | Axenfeld-Rieger Syndrome | Azoospermia | B-cell Chronic Lymphocytic Leukemia | B-cell Prolymphocytic Leukemia | Babesiosis | Bacterial Meningitis | Bainbridge-Ropers Syndrome | Barakat Syndrome | Bardet-Biedl Syndrome | Bare Lymphocyte Syndrome | Barrett Esophagus | Bartsocas-Papas Syndrome | Bartter Syndrome | Basal Cell Nevus Syndrome | Basal Ganglia Cerebrovascular Disease | Basal Ganglia Disease | Basal Ganglia Disease, Biotin-responsive | Basan Syndrome | Batten Disease | Beare-Stevenson Syndrome | Becker Muscular Dystrophy | Beckwith-Wiedemann Syndrome | Behavioral Variant Of Frontotemporal Dementia | Behcet's Disease | Benign Familial Infantile Seizures | Benign Familial Neonatal Convulsions | Benign Familial Pemphigus | Benign Hereditary Chorea | Benign Recurrent Intrahepatic Cholestasis 1 | Bernard-Soulier Syndrome | Best Macular Dystrophy | Beta-Propeller Protein-associated Neurodegeneration | Bethlem Myopathy | Bicuspid Aortic Valve | Bietti Crystalline Dystrophy | Binge Eating Disorder | Biotinidase Deficiency | Bipolar Disorder | Birk-Barel Syndrome | Birt-Hogg-Dube Syndrome | Bladder Exstrophy | Blastoma, Pleuropulmonary | Blastomycosis | Blau Syndrome | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Blepharitis | Blepharo-cheilo-odontic Syndrome | Blepharoconjunctivitis | Blepharophimosis Syndrome | Blepharospasm | Blomstrand Osteochondrodysplasia | Blood Protein Disorders | Bloom Syndrome | Blue Nevus | Blue Rubber Bleb Nevus Syndrome | Bone Giant Cell Tumor | Bone Marrow Necrosis | Borderline Personality Disorder | Borjeson-Forssman-Lehmann Syndrome | Botulism | Brachial Plexus Neuropathy | Brachydactyly | Branchiootorenal Syndrome | Brenner Tumor | Bronchiectasis | Bronchiolitis | Bronchitis | Bronchitis, Chronic | Brooke-Spiegler Syndrome | Bruck Syndrome | Brugada Syndrome 1 | Budd-Chiari Syndrome | Bulimia Nervosa | Bullous Pemphigoid | Burn-McKeown Syndrome | Bursitis | C3 Glomerulonephritis | C3 Glomerulopathy | Cabezas Syndrome | Calcium Pyrophosphate Deposition Disease | Campomelic Dysplasia | Camptocormia | Camurati-Engelmann Disease | Canavan Disease | Cancer, Bladder | Cancer, Brain | Cancer, Breast | Cancer, Colon | Cancer, Kidney | Cancer, Lung | Cancer, Prostate | Cancer, Skin | Cannabis Abuse | Cantu Syndrome | Carbamoyl Phosphate Synthetase I Deficiency | Carbohydrate Metabolism Disorders | Carbonic Anhydrase VA Deficiency | Carcinoid Syndrome | Carcinoid Tumor | Carcinoma In Situ | Carcinoma, Merkel Cell | Carcinoma, Signet Ring Cell | Carcinoma, Small Cell | Carcinoma, Squamous Cell | Carcinoma, Transitional Cell | Cardiac Arrest | Cardiac Sarcoidosis | Cardiofaciocutaneous Syndrome | Cardiomyopathy, Dilated, 1L | Cardiomyopathy, Hypertrophic | Cardiomyopathy, Peripartum | Cardiomyopathy, Restrictive | Cardiospondylocarpofacial Syndrome | Carey-Fineman-Ziter Syndrome | Carney Triad | Carney-Stratakis Syndrome | Carotid Artery Disease | Carpal Tunnel Syndrome | Carpenter Syndrome | Cartilage Disorders | Castleman Disease | Cat Eye Syndrome | Cataplexy | Cataract | Cavitary Optic Disc Anomalies | CDKL5 Deficiency Disorder | CEDNIK Syndrome | Celiac Disease | Cellulitis | Cenani-Lenz Syndactyly Syndrome | Central Core Disease | Central Pain Syndrome | Central Retinal Artery Occlusion | Centronuclear Myopathy | Cerebellar Ataxia, Cayman Type | Cerebellofaciodental Syndrome | Cerebral Amyloid Angiopathy | Cerebral Cavernous Malformations | Cerebrotendinous Xanthomatosis | Cerebrovascular Disorders | Cervical Dystonia | Cervicitis | Chanarin-Dorfman Syndrome | Charcot-Marie-Tooth Disease | Charcot-Marie-Tooth Disease Axonal Type 2N | Charcot-Marie-Tooth Disease Type 2D | Charcot-Marie-Tooth Disease Type 2E | Charcot-Marie-Tooth Disease Type 2T | Charcot-Marie-Tooth Disease Type 3 | Charcot-Marie-Tooth Disease Type 4 | Charcot-Marie-Tooth Disease Type 4B1 | Charcot-Marie-Tooth Disease Type 4D | Charcot-Marie-Tooth Disease Type 4E | Charcot-Marie-Tooth Disease, Type 1A | Charcot-Marie-Tooth Disease, Type 2 | Charcot-Marie-Tooth Disease, Type 2A | Charcot-Marie-Tooth Disease, Type 2C | Charcot-Marie-Tooth Disease, Type 6 | CHARGE Syndrome | Chediak-Higashi Syndrome | Cheilitis | Cherubism | Chiari Malformation Type I | Chitayat Syndrome | Chloridorrhea, Congenital | Cholangiocarcinoma | Cholangitis | Cholecystitis | Cholelithiasis | Cholera | Cholestasis | Cholestasis, Intrahepatic | Cholesteryl Ester Storage Disease | Chondrodysplasia Punctata | Chondrodysplasia Punctata 1, X-linked Recessive | Chondrodysplasia Punctata 2, X-linked Dominant | Chondroma | Chondromyxoid Fibroma | Chondrosarcoma | CHOPS Syndrome | Chordoid Glioma | Chordoma | Chorea | Chorea-acanthocytosis | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Choriocarcinoma | Chorioretinitis | Choroideremia | Choroiditis | Christianson Syndrome | Chromosome 16p11.2 Deletion Syndrome | Chromosome 17q21.31 Deletion Syndrome | Chromosome 5q Deletion Syndrome | Chromosome 8q21.11 Deletion Syndrome | Chromosome 9q34.3 Deletion Syndrome | Chronic Beryllium Disease | Chronic Enteropathy Associated With SLCO2A1 Gene | Chronic Granulomatous Disease | Chronic Granulomatous Disease, X-linked | Chronic Idiopathic Myelofibrosis | Chronic Inflammatory Demyelinating Polyneuropathy | Chronic Kidney Disease | Chronic Leukemia | Chronic Lymphocytic Leukemia | Chronic Mucocutaneous Candidiasis | Chronic Myeloid Leukemia
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