Drug Database
TH

theophylline (Teonova syrup / Theodur Sprinkle / Theolan suspension)

✓ Approved

Mitsubishi Tanabe Pharma Corporation · ADORA1 · Small Molecule

What is theophylline?

theophylline is a small molecule developed by Mitsubishi Tanabe Pharma Corporation. It is approved for therapeutic indications via oral (po).

Drug Profile

Brand NamesTeonova syrup, Theodur Sprinkle, Theolan suspension
CompanyMitsubishi Tanabe Pharma Corporation
Drug ClassSmall Molecule
Molecular TargetADORA1, ADORA2A
RouteOral (PO)
StatusApproved

Mechanism of Action

Molecular Targets

theophylline acts on 2 molecular targets:

ADORA1adenosine A1 receptor (RDC7)
ADORA2Aadenosine A2a receptor (A2aR, RDC8)
Want deeper analysis?Noah AI can explain complex mechanisms and compare to similar drugs.

Therapeutic Indications

theophylline is developed for 2 unique indications across 1 therapeutic area.

Therapeutic AreaConditionPhase
Respiratory, thoracic and mediastinal disordersAsthma✓ Approved
Respiratory, thoracic and mediastinal disordersRespiratory disorder✓ Approved

Related Research Articles

PubMedNucleic acids research2026-07-14

Engineering aptamer dimers (apdimers) for optimization of synthetic riboswitches.

Hedwig Vera V, Müller Elisabeth E, Ketterer Stephanie S, Lang Isabel I et al.

Riboswitches are compact RNA-based regulatory elements capable of modulating gene expression in response to small molecules, without the need for additional proteins. Various synthetic riboswitches have been engineered using in vitro-generated tetracycline and theophylline aptamers. However, many of these constructs exhibit suboptimal switching efficiency and background expression. Moreover, efforts to enhance their performance often involve time-consuming and costly screening processes. Here we report that artificial riboswitches can be efficiently optimized by engineering fusion aptamers that contain two binding pockets (apdimers). Following this rational approach, we generated cooperativity between both binding pockets, resulting in the improved performance of splicing-based and ribozyme-based synthetic riboswitches. We finally combined optimized tetracycline switches, yielding dynamic ranges exceeding 1000-fold with minimal background expression in the OFF state. In addition, we show that the optimized tetracycline riboswitches can be used to efficiently induce AAV-mediated transgene expression in mice. The presented strategy offers a straightforward and effective approach for the optimization of existing synthetic riboswitches and the design of novel riboswitches.

PubMedFrontiers in plant science2026-07-13

A task-specific architecture with multi-scale attention and shape-aware loss for strawberry phenophase recognition in complex fields.

Li Shilin S, Guo Shangjian S, Yang Nan N, Sun Lili L et al.

To address the challenges of recognizing small strawberry targets and achieving accurate phenological perception in complex field environments, this paper proposes a novel end-to-end lightweight detection architecture named HCMS-Net. The backbone is a Residual Efficient Layer Aggregation Network (R-ELAN) enhanced with a Multi-Scale Convolutional Attention (MSCA) mechanism, which emphasizes subtle color and texture variations to differentiate key phenological phases. For feature fusion, hypergraph convolution (from HyperC2Net) and a Mixed Aggregation Network (MANet) are incorporated, modeling the clustered morphology of strawberries and strengthening the representation of sparse small fruits. The detection head incorporates a lightweight Conv2Former module to capture long-range dependencies and spatial contextual information across growth stages, thereby enhancing the model's capacity to represent continuous phenological changes. A Shape-Normalized Wasserstein Distance (Shape-NWD) loss is introduced to stabilize optimization against minor pixel deviations. Experimental results demonstrated that HCMS-Net achieved a mean average precision (mAP) of 94.9% and an F1-score of 90.0%. Specifically, the average precision (AP) values for the flowering, young fruit, green fruit, veraison, and mature fruit stages reached 99.3%, 88.3%, 90.9%, 97.0%, and 98.2%, respectively. Heatmaps confirmed HCMS-Net's precise attention focus across all five phenological stages, effectively suppressing irrelevant backgrounds. Compared to ten mainstream detectors, HCMS-Net surpassed alternatives such as RT-DETR and the YOLOv5n to v13n by 3.4-8.0 percentage points in mAP. It even surpassed YOLOv12s by 2.7 percentage points, while containing only 32.86% of its parameters. The model offers high accuracy and efficiency for phenological period detection, supporting selective harvesting and intelligent agricultural management.

PubMedPakistan journal of pharmaceutical sciences2026-07-12

Pharmacokinetic interaction between evodiamine and doxofylline in rats.

Lin Yuxian Y, Yang Yongle Y, Luo Wang W, Chen Yangfang Y et al.

Doxofylline (DFL) is a medication widely employed in the management of asthma and chronic obstructive pulmonary disease. Evodiamine (EVO), a bioactive alkaloid from traditional Chinese medicine (TCM), is commonly utilized for treating hypertension, gastropathy, and eczema. Cytochrome P450 enzymes primarily mediate the metabolism of both pharmaceuticals and TCMs in-vivo, which potentially lead to drug-drug interactions. This study aimed to investigate the effects of oral EVO on the pharmacokinetics (PK) of DFL and its metabolite, theophylline (TPL), in rats. Twelve rats were randomly assigned to control and experimental groups. The experimental group received 50 mg/kg EVO orally once daily for one week, while the control group received 0.5% sodium carboxymethyl cellulose. On day 7, DFL (80 mg/kg) was administered 2 h post-treatment. Venous blood specimens were collected from the retro-orbital venous plexus at 0.1667, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 12, 24 and 48 h post-dose. Plasma concentrations of DFL and TPL were analyzed by liquid chromatography-tandem mass spectrometry (LC-MS/MS). Compared with the control group, the experimental group showed significant alterations in several PK parameters for both DFL and TPL. The administration of EVO markedly increased MRT(0-∞), MRT(0-t), VRT(0-∞), VRT(0-t), t1/2z, and Vz/F for DFL while also enhancing CLz/F and Vz/F for TPL. Conversely, EVO notably decreased AUC(0-∞), AUC(0-t), and MRT(0-t) values associated with TPL. Concomitant administration of EVO alongside DFL resulted in substantial modifications to key PK parameters concerning both DFL and its metabolite TPL in rats. Specifically, EVO prolonged the retention time and increased the volume of distribution of DFL, while simultaneously reducing the bioavailability and accelerating the clearance of TPL (P<0.05). Therefore, it is imperative to closely monitor the impact of TCM EVO on the PKs of DFL and TPL in experimental animals, necessitating further research and clinical observation.

PubMedTranslational and clinical pharmacology2026-07-08

Development and evaluation of automated screening algorithms for pre-analytical errors in pharmacokinetic data: a simulation-based study.

Shim Minsub M, Kang Jaegu J, Yu Kyung-Sang KS, Huh Ki Young KY

Pre-analytical errors such as sample mix-ups can compromise the integrity of pharmacokinetic (PK) data. We simulated vancomycin PK data and introduced two error types: intra-individual time point swap (TS) errors and inter-individual concentration swap (CS) errors. This study developed and validated two automated detection approaches-a run-test-based non-parametric method and a Mahalanobis distance-based method with leave-one-out cross-validation (LOOCV)-for identifying pre-analytical errors in PK datasets. Performance was evaluated using 12,500 simulated profiles comparing the two methods. The distance-based method demonstrated significantly higher error detection rate (79.7% vs. 59.6%, p < 0.001) and greater area under the receiver operating characteristic curve (0.856; 95% confidence interval [CI], 0.816-0.889 vs. 0.574; 95% CI, 0.541-0.610) compared to the run-test, while maintaining reasonable specificity (76.4% vs. 84.0%). For TS errors, the distance-based method achieved higher recall (80.4% vs. 71.9%) and modestly higher F1-score (0.530 vs. 0.515). For CS errors, the distance-based method demonstrated superior precision (86.1% vs. 59.8%) with comparable F1-score (0.572 vs. 0.564). Detection was robust across alternative PopPK models, a structurally different drug (theophylline), training-set contamination (with the minimum covariance determinant estimator recommended for non-curated training), missing data (with sub-vector marginal handling), and sampling-time jitter. Overall, the distance-based method with LOOCV outperformed the conventional run-test across key performance metrics and can serve as a practical quality control tool for ensuring PK data integrity in clinical pharmacology research.

PubMedEuropean journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences2026-07-08

Antisolvent crystallization of indomethacin cocrystals: influence of coformers and solvent systems.

Pardo Hugo H, Guarnizo-Herrero Víctor V, Martínez-Alonso Borja B, Torrado-Salmerón Carlos C et al.

Indomethacin (IND), a Biopharmaceutics Classification System (BCS) Class II drug, exhibits poor aqueous solubility and low dissolution rate, which may limit its oral absorption. In this study, IND cocrystals with benzoic acid (AcBz), theophylline (THP), and caffeine (CAF) were prepared to improve their in vitro dissolution performance. Saturated solutions of IND and each coformer in methanol (MeOH) or ethanol (EtOH) were subjected to dropwise addition of water as antisolvent at solvent/antisolvent volume ratios of 1:0.5, 1:1, and 1:2. The resulting solids were collected by vacuum filtration, dried for 24 h, and characterised by PXRD, FT-IR, DSC, and SEM. Dissolution data were statistically analysed using three-way ANOVA (p < 0.05). Solid-state characterisation supported the formation of new crystalline phases in the IND-AcBz, IND-THP, and IND-CAF systems. PXRD patterns showed distinctive reflections within the 2θ range of 6-15°, while FT-IR spectra revealed shifts in the 1600-1700 cm⁻¹ region, consistent with changes in intermolecular hydrogen bonds. DSC thermograms further supported the formation of new solid phases through melting endotherms distinct from those of the parent compounds. Three-way ANOVA showed that solvent type, coformer selection, and solvent/antisolvent ratio significantly influenced the dissolution profiles. The 1:1 solvent/antisolvent ratio produced the most favourable systems, with IND-AcBz prepared in MeOH showing the best release profile and significantly outperforming pure IND, with a 53.7% increase in cumulative drug release at 1 h Overall, these results indicate that antisolvent cocrystallisation is an effective strategy for improving the solid-state properties and in vitro dissolution behaviour of IND. In particular, the 1:1 solvent/antisolvent was associated with improved crystalline quality and enhanced dissolution performance, highlighting the potential of engineered cocrystals as a formulation strategy to address solubility-related limitations in poorly water-soluble drugs.

PubMedActa crystallographica. Section C, Structural chemistry2026-07-07

Effect of molecular perturbation on cocrystal formation: theophylline and its 8-halo analogues with flavonoids.

Ye Weijian W, Sung Herman H Y HHY, Williams Ian D ID

The tendency for cocrystal formation between alkaloids and flavonoids is found to be quite common (around 30%) and based on the optimization of hydrogen-bond formation between the acceptor-rich alkaloids and donor-rich flavonoids. Within each molecular family there is substantial variation in cocrystal tendency, leading to considerable scope for selective cocrystal precipitation to assist in the separation of complex mixtures of these natural product families. Theophylline (C7H8N4O2) follows caffeine and theacrine in forming a substantial number of flavonoid cocrystals - six in total, of which three were reported previously. By contrast, the 8-halo-substituted analogues 8-X-Tph [X = Cl (C7H7ClN4O2), Br (C7H7BrN4O2)] form cocrystals with just myricetin (C15H10O8) and kaempferol (C15H10O6). Weakening of the acceptor capability of the alkaloid N9 atom upon proximal halo substitution may play a role in the reduced tendency of 8-X-Tph towards cocrystal formation, since improved packing efficiency is not a key factor in the formation of these cocrystals. Most of the cocrystal phases may be conveniently prepared with good yield and purity through either liquid-assisted grinding (LAG) or microwave-assisted cocrystallization from 1-butanol.

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