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

PubMedScandinavian journal of pain2026-07-24

Multimodal deep learning fusion for automatic pain detection in cancer patients.

Cascella Marco M, Mariani Fabio F, Barberio Daniela D, Crispo Anna A et al.

Since pain is a multidimensional and subjective experience, pain assessment remains challenging. With advances in artificial intelligence (AI), automatic pain assessment (APA) systems offer a valuable opportunity for objective pain evaluation. However, most approaches focus on a single modality. In this proof-of-concept study, exploring multimodal fusion strategies in a controlled experimental setting, we present a deep learning framework for multimodal fusion that combines facial, acoustic, and textual information to improve APA in cancer patients. A multimodal dataset was created from video-recorded interviews with oncologic patients. In Phase I, audio, video, and transcripts were segmented at the sentence level and temporally aligned using the Eudico Linguistic Annotator (ELAN) to ensure frame-level correspondence across modalities. In Phase II, modality-specific features were extracted: Facial Action Units from OpenFace, acoustic descriptors (MFCCs, chroma, spectral contrast, and Mel-spectrogram) from a dedicated speech-processing pipeline, and sentence-level textual embeddings from ITA-BERT. During training, the most effective analytical strategy was chosen through knowledge transfer approaches. The ELAN-assisted annotation pipeline streamlined expert labeling. Two architectures were implemented and compared: bimodal autoencoder fusion models and a transformer-based model with pairwise cross-modal attention. These models were trained and evaluated using subject-independent and stratified 5-fold cross-validation. To address the lack of independence between segments, a strictly subject-independent cross-validation strategy was adopted. Knowledge transfer using pretrained large-scale models outperformed traditional feature-based approaches and was applied to multimodal pain detection. Multimodal models achieved performance comparable to the strongest unimodal modality (text), while showing improved balance across modalities, suggesting potential complementary effects. Both multimodal architectures demonstrated high accuracy in distinguishing between pain and non-pain classes. The bimodal autoencoder achieved stable results across folds, with a mean accuracy of about 80 % and balanced error distribution. The pairwise transformer with cross-modal attention achieved similar performance, with smooth training and validation loss curves. No evident divergence between training and validation loss curves was observed across folds, suggesting stable behavior within the cross-validation setting. However, subject-level overfitting cannot be excluded given the limited sample size. Multimodal fusion enhances system robustness by integrating complementary signals. Despite limitations and the need for improvement, multimodal deep learning strategies can support the detection of observable pain-related expressions.

PubMedChembiochem : a European journal of chemical biology2026-07-24

Reconsidering Molecular Docking Practices in Aptamer Research.

Xie Yachen Y, Liu Juewen J

Molecular docking is increasingly used to infer aptamer-target interactions, yet most studies rely on computationally predicted aptamer structures rather than experimentally determined ones. Using a benchmark set of aptamers with known high-resolution structures, we show that commonly used modeling approaches, including RNAComposer and AlphaFold3, fail to reliably reproduce aptamer conformations, particularly at the binding sites critical for molecular recognition. Key limitations include the use of A-form RNA models to represent B-form DNA structures, the prediction of ligand-free rather than ligand-bound conformations, and the scarcity of experimentally determined aptamer structures for training machine-learning models. Using the theophylline aptamer, for which high-resolution structures are available in both DNA and RNA forms, we systematically evaluated each step of the standard docking workflow. We found that structure-prediction errors generate incorrect binding pockets, docking scores fail to distinguish theophylline from caffeine despite a 250,000-fold difference in affinity, and molecular dynamics simulations do not overcome these shortcomings. Together, these results reveal fundamental weaknesses in current aptamer docking workflows and caution against using docking-derived models to infer binding mechanisms in the absence of experimental structural data.

PubMedLaterality2026-07-23

Hemispheric specialization for imitating hand-head positions and finger configurations - A study with hemispherectomy individuals.

Ketter Laura L, Ptito Alain A, Augenstein Maximilian M, Lausberg Hedda H

Imitation deficits after brain damage are commonly assessed with meaningless hand positions (HP) and finger configurations (FP). Previous studies on unilateral brain damage and callosotomy individuals revealed left-hemispheric specializations for HP and bilateral representation for FP, with a right-hemispheric dominance. This study examined hemispheric specialization for HP and FP imitation, as well as FP subtypes, in five hemispherectomy individuals (n = 3 with a remaining left (rLH); n = 2 with a remaining right hemisphere (rRH)). Imitation performance was analysed with the NEUROGES®-ELAN system, considering error types and reaction times. Bayesian analyses revealed no group differences in performance scores, error types and reaction times for HP or FP imitation. The qualitative analysis of error types revealed group differences, particularly for FP imitation, with rRH individuals showing predominantly self-corrections, whereas rLH individuals showed diverse error patterns (e.g., position errors). However, considerable interindividual variability was foremost observed across imitation tasks and subtypes. Overall, the findings do not support a strict hemispheric specialization for HP and FP imitation following hemispherectomy. Rather, they highlight the importance of individual variability.

PubMedThe Journal of organic chemistry2026-07-19

Metal-Free Radical Carbamoylation/Cyclization for Divergent Synthesis of Six- to Eight-Membered Benzimidazole-Fused Heterocycles.

Cao Haidong H, Yin Shuangying S, Yao Ming M, Zhang Xiangtao X et al.

A metal-free radical tandem carbamoylation/cyclization strategy for the divergent synthesis of benzimidazole-fused heterocycles has been described. Using commercially available oxamic acids and imidazoles tethered with unactivated alkenes under mild conditions, this method provides the first efficient access to stable [6,5,7]- and [6,5,8]-fused frameworks along with [6,5,6] systems. It exhibits excellent functional group tolerance and broad substrate scope, including 2-heteroarylbenzimidazoles. Preliminary studies also revealed that monoalkyl oxalates can serve as effective radical precursors in this transformation, offering potential for further derivatization of the products. The method is also applicable to the late-stage diversification of bioactive molecules, such as theophylline.

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.

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