Powered by AI technology, BDE-Bio combines massive literature, patent and comprehensive biological data to accurately screen and predict disease diagnosis and therapeutic targets / biomarkers. It can automatically generate target research reports with one click, making it an indispensable tool for pharmaceutical research and development.
BDE-Bio
TARGET PRECISE DISCOVERY
Product Introduction
BDE-Bio achieves precise screening and prediction of new targets by combining 24-hour continuous updates, massive literature texts, comprehensive biological databases, and large-scale multi-omics data, and can provide the basis and logic for target discovery.
1) Capture: 24-hour monitoring of Pubmed, 24 public databases (genecard, drugbank, pubchem, etc.), real-time inbound parsing.
2) Extraction: It can extract basic information about the target, protein structure, biological mechanism of the target, drug resistance of the target, disease correlation, etc.
3) Analysis: Summarize long content, generate reports with one click, recommend target points, etc.
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.
Common Targets and Diseases
Targets
ABCB1 | ABCG2 | ACE2 | AHR | AKT1 | ALK | AR | ATM | BAX | BCL2 | BCL2L1 | BECN1 | BRAF | BRCA1 | CAMP | CASP3 | CASP9 | CCL5 | CCND1 | CD274 | CD4 | CD8A | CDH1 | CDKN1A | CDKN2A | CREB1 | CXCL8 | CXCR4 | DNMT1 | EGF | EGFR | EP300 | ERBB2 | EREG | ESR1 | EZH2 | FN1 | FOXO3 | HDAC9 | HGF | HMGB1 | HSP90AA1 | HSPA4 | HSPA5 | IDO1 | IFNA1 | IGF1 | IGF1R | IL17A | IL6 | INS | JUN | KRAS | MAPK1 | MAPK14 | MAPK3 | MAPK8 | MAPT | MCL1 | MDM2 | MET | MMP9 | MTOR | MYC | NFE2L2 | NLRP3 | NOTCH1 | PARP1 | PCNA | PDCD1 | PLK1 | PRKAA1 | PRKAA2 | PTEN | PTGS2 | PTK2 | RELA | SIRT1 | SLTM | SMAD4 | SOD1 | SQSTM1 | SRC | STAT1 | STAT3 | STAT5A | TAK1 | TERT | TLR4 | TNF | TP53 | TXN | VEGFA | YAP1
Diseases
Antley-Bixler Syndrome | Dental Caries | Wolfram Syndrome | McLeod Syndrome | VACTERL/VATER Association | Coronary Restenosis | Persistent Fetal Circulation | Neurofibromatosis-Noonan Syndrome | Analgesia | Hereditary Coproporphyria | D-2-Hydroxyglutaric Aciduria | Primrose Syndrome | Currarino Syndrome | Tonsillitis | Pontocerebellar Hypoplasia | Juvenile Myelomonocytic Leukemia | Acute Myeloid Leukemia | Pneumonia, Bacterial | Cardiomyopathy, Restrictive | Eiken Syndrome | Neovascular Glaucoma | Spinocerebellar Ataxia Type 23 | Scleroderma | Cryptococcal Meningitis | Paternal Uniparental Disomy Of Chromosome 14 | Neurofibrosarcoma | Keratitis | Antithrombin III Deficiency | Heart Block | Gardner Syndrome | Cannabis Abuse | Glycogen Storage Disease Type 1b | Congenital Hereditary Endothelial Dystrophy Type II | Peutz-Jeghers Syndrome | Panniculitis | Amenorrhea | Salla Disease | Basal Ganglia Disease, Biotin-responsive | Rash | Major Depression | Colitis, Collagenous | Ehlers-Danlos Syndrome | Hereditary Hemorrhagic Telangiectasia | Hyperthyroidism | Atrioventricular Septal Defect | Pulmonary Tuberculosis | Rett Syndrome | Osteogenesis Imperfecta Type III | Oligoasthenoteratozoospermia | Adenylosuccinate Lyase Deficiency | Renal Dysplasia | Exostoses | Neurocutaneous Melanocytosis | Hereditary Neuropathy With Liability To Pressure Palsies | Alzheimer Disease, Late Onset | Woodhouse-Sakati Syndrome | Sensory Neuropathy | Ollier Disease | Hyperostosis | Agranulocytosis | Charcot-Marie-Tooth Disease Type 4B1 | Uremia | Dyslipidemia | Menkes Disease | Hypolipoproteinemia | Autonomic Neuropathy | X-linked Myotubular Myopathy | Myasthenia | Osteonecrosis Of The Jaw | Melnick-Needles Syndrome | Pyoderma Gangrenosum | Prediabetes | 3-hydroxy-3-methylglutaric Aciduria | Echinococcosis | Schwannomatosis | Micro Syndrome | Premenstrual Syndrome | Intestinal Pseudo-obstruction | Frontometaphyseal Dysplasia | Hemoglobinopathies | Neurocysticercosis | Congenital Absence Of Vas Deferens | Seminoma | Esophageal Motility Disorders | Coenzyme Q10 Deficiency | Ganglioneuroma | Blastomycosis | Hemochromatosis | Heavy Chain Disease | Mosaic Variegated Aneuploidy Syndrome 2 | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Hyperoxaluria | Carney-Stratakis Syndrome | Spinocerebellar Ataxia Type 27 | Optic Atrophy 2 | Malaria, Cerebral | Arterial Tortuosity Syndrome | Pilomatrix Carcinoma | Posterior Polar Cataract | Geleophysic Dysplasia | Adenoid Cystic Carcinoma | Epidermolytic Ichthyosis, Annular | Apert Syndrome | Charcot-Marie-Tooth Disease Type 4E | Early Infantile Epileptic Encephalopathy 1 | Usher Syndrome Type I | Focal Dermal Hypoplasia | POEMS Syndrome | Agnathia-Otocephaly Complex | Prolymphocytic Leukemia | Distal Spinal Muscular Atrophy | Desmosterolosis | Thalassemia, Beta | Communication Disorders | Congenital Hypofibrinogenemia | Lentigo | Pulverulent Zonular Cataract | Thanatophoric Dysplasia | Acute Lung Injury | Nephropathy | Skin Fragility-woolly Hair Syndrome | Keratocystic Odontogenic Tumor | Gallstones | Retinoblastoma | Meniere's Disease | Porphyria, Variegate | Thyroiditis, Autoimmune | Progressive Familial Intrahepatic Cholestasis Type 3 | Porencephaly | Empyema | Vertebrobasilar Insufficiency | Hypoparathyroidism | Subacute Sclerosing Panencephalitis | Disseminated Superficial Actinic Porokeratosis | Fundus Albipunctatus | Paroxysmal Nocturnal Hemoglobinuria | Vitamin A Deficiency | Familial Episodic Pain Syndrome | Becker Muscular Dystrophy | Nasodigitoacoustic Syndrome | Erythrokeratodermia Variabilis | Methemoglobinemia | Juvenile Hyaline Fibromatosis | Peripheral T-cell Lymphoma | Cheilitis | Japanese Encephalitis | Non-proliferative Diabetic Retinopathy | Apparent Mineralocorticoid Excess Syndrome | Epidermolysis Bullosa | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Protein C Deficiency | AIDS | Congenital Disorders Of Glycosylation | Angioedema, Acquired | Ophthalmia, Sympathetic | HANAC Syndrome | Facioscapulohumeral Muscular Dystrophy Type 1 | Sandhoff Disease | Stargardt Disease | Cri-du-chat Syndrome | Ophthalmoplegia | Methemoglobinemia Type IV | Neurofibromatosis | Sclerosteosis | Birk-Barel Syndrome | Polycythemia | Silver-Russell Syndrome | Chylomicron Retention Disease | Familial Retinal Arterial Macroaneurysm | Hyper IgE Syndrome | Rosacea | Bronchiectasis | Diabetic Macular Edema | Spondylometaphyseal Dysplasia | Multicystic Renal Dysplasia | Nail Disorder, Nonsyndromic Congenital | Potocki-Shaffer Syndrome | Chromosome 16p11.2 Deletion Syndrome | Diabetes Insipidus, Neurogenic | Thyroid Hormone Resistance | Sarcoma, Ewing | Benign Hereditary Chorea | Pulmonary Alveolar Proteinosis | Bruck Syndrome | Non-small Cell Lung Cancer | Hyperammonemia | Nance-Horan Syndrome | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Nicotine Dependence | Mucolipidosis Type II | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Epilepsy Of Infancy With Migrating Focal Seizures | Joubert Syndrome | Axenfeld-Rieger Syndrome | Otopalatodigital Syndrome Type 2 | Light Chain Amyloidosis | Scoliosis | Trigonocephaly | Biotinidase Deficiency | Heimler Syndrome | Miyoshi Myopathy | Schizotypal Personality Disorder | Microvillus Inclusion Disease | Constipation | Cousin Syndrome | Hypotonia-cystinuria Syndrome | Open-angle Glaucoma | Albinism | Aarskog-Scott Syndrome | Oculocutaneous Albinism | Liver Failure, Acute Infantile | Congenital Aniridia | Pleural Tuberculosis | 3C Syndrome | Anti-NMDA Receptor Encephalitis | Syphilis | Lupus Erythematosus | Hypohidrotic Ectodermal Dysplasia, X-linked | Riboflavin Transporter Deficiency Neuronopathy | Pneumonia, Mycoplasma | Sarcoidosis | Meningococcal Meningitis | Cirrhosis | Tyrosinemia Type 2 | Mumps | Purpura | Nephroblastoma | Proximal Symphalangism | Cocaine-Related Disorders | Esophagitis, Eosinophilic | Senior-Loken Syndrome | Chylothorax, Congenital | Specific Granule Deficiency | Usher Syndrome Type II | Tracheal Disorders | Congenital Heart Defects | Emery-Dreifuss Muscular Dystrophy | Acute Motor Axonal Neuropathy | Tardive Dyskinesia | Hereditary Spastic Paraplegia | Moyamoya Disease | Paraganglioma | Myopia | Crimean-Congo Hemorrhagic Fever | Neurofibroma | Azoospermia | Amyotrophic Lateral Sclerosis, Juvenile | Methylmalonic Acidemia | Sialidosis | Mabry Syndrome | Scleroderma, Diffuse | Angiosarcoma Of The Breast | Systemic Lupus Erythematosus | Silicosis | IgA Deficiency | Kidney Stones | Diabetes Insipidus | Costello Syndrome | Meningococcal Infections | Hypotrichosis Simplex | Acrodermatitis Enteropathica | Juvenile Myoclonic Epilepsy | Pityriasis Rubra Pilaris | Premature Ejaculation | Early Infantile Epileptic Encephalopathy | Chondrosarcoma | Tyrosinemia Type 1 | Cardiospondylocarpofacial Syndrome | Pure Autonomic Failure | Facioscapulohumeral Muscular Dystrophy Type 2 | Lipoma | Peripheral Neuropathy | Hemochromatosis Type 2 | Anterior Segment Dysgenesis | Xeroderma Pigmentosum | Pituitary Disorders | Eclampsia | Mevalonate Kinase Deficiency | Transcobalamin Deficiency | Alkaptonuria | Neurogenic Bladder | Babesiosis | Connective Tissue Disorders | Basan Syndrome | Fibrosarcoma | Meningioma, Benign | Giant Cell Arteritis | Thyroiditis | Anorectal Fistula | Acute Generalized Exanthematous Pustulosis | Erythropoietic Protoporphyria | Familial Glucocorticoid Deficiency | Stromal Corneal Dystrophy | Pseudohermaphroditism | Branchiootorenal Syndrome | Oral Lichen Planus | Acne | Atelosteogenesis Type 2 | Extramammary Paget's Disease | Peters-plus Syndrome | Pierpont Syndrome | Perivascular Epithelioid Cell Tumor | Pseudohypoparathyroidism Type 1A | Dystonia-parkinsonism, X-linked | Corticobasal Syndrome | Cryopyrin-associated Periodic Syndromes | Goiter, Nodular | Arrhythmogenic Right Ventricular Cardiomyopathy | Cholestasis, Intrahepatic | LRBA Deficiency | Osteosarcoma | Hemangioendothelioma | Multiple System Atrophy | Papillon-Lefevre Syndrome | Diabetes | Pachyonychia Congenita | Congenital Afibrinogenemia | Cerebral Amyloid Angiopathy | Aneurysm, Abdominal Aortic | Spinocerebellar Ataxia Type 16 | Glaucomatocyclitic Crisis | Spinocerebellar Ataxia Type 28 | Snyder-Robinson Syndrome | Waardenburg Syndrome Type 4 | Pulmonary Capillary Hemangiomatosis | Diffuse Mesangial Sclerosis | Chondrodysplasia Punctata 1, X-linked Recessive | Gastroschisis | Hyperinsulinemia | Pearson Syndrome | Beckwith-Wiedemann Syndrome | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Inflammatory Joint Disease | Pemphigus | Primary Carnitine Deficiency | Sclerocornea | Hereditary Pyropoikilocytosis | Colitis, Lymphocytic | Stuttering | Hypereosinophilic Syndrome | FG Syndrome | Schistosomiasis Mansoni | Pathological Gambling | Sleep Apnea | Carcinoma, Squamous Cell | Cantu Syndrome | Headache | Glioblastoma | Isovaleric Acidemia | Tetanus | Usher Syndrome Type III | Acute Coronary Syndrome | Cholera | Monilethrix | Bloom Syndrome | Spinocerebellar Ataxia Type 13 | Rhabdoid Tumor | Thyrotoxic Periodic Paralysis | Juvenile Polyposis | Keratoacanthoma | Auriculocondylar Syndrome | Niemann-Pick Disease, Type C | Narcolepsy | PHARC Syndrome | Bare Lymphocyte Syndrome | Granuloma Annulare | Glycogen Storage Disease Type 5 | Congenital Nystagmus | Pure Red Cell Aplasia | Orotic Aciduria | Oculocutaneous Albinism Type 2 | Occipital Neuralgia | Glycogen Storage Disease Type 3 | Nicotine Addiction | MELAS Syndrome | Lipodystrophy | Megalencephaly | Hepatitis D | Hepatitis, Alcoholic | Congenital Ichthyosiform Erythroderma | Inflammatory Linear Verrucous Epidermal Nevus | Thrombocythemia, Essential | Otitis Media | Eccrine Porocarcinoma | Lymphangioleiomyomatosis | Renal Hypouricemia | Diamond-Blackfan Anemia | Hypoplastic Left Heart Syndrome | Large Granular Lymphocytic Leukemia | Cancer, Brain | Leri Pleonosteosis | Spinal Muscular Atrophy Type 2 | Pulmonary Stenosis | Cyst | Mitochondrial DNA Depletion Syndrome 13 | Atelosteogenesis Type 1 | Pyruvate Kinase Deficiency | Wolff-Parkinson-White Syndrome | Choriocarcinoma | Cardiomyopathy, Dilated, 1L