Evidence map›Paper›PMID 41462364›Full record

ArticleJournal of cheminformatics2025

CalVSP: a program for analyzing the molecular surface areas, volumes, and polar surface areas.

Yuzhu Li, Daiju Yang, Qingyi Shi, Weidong Zhang, Qingyan Sun

Abstract read
In one paragraph

Article in Journal of cheminformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Yuzhu LiSchool of Pharmaceutical Sciences, Shanghai Jiao Tong University, Shanghai, 200240, China.
Daiju YangNational Key Laboratory of Lead Druggability Research, Shanghai Institute of Pharmaceutical Industry, China State Institute of Pharmaceutical Industry, Shanghai, 201203, China.
Qingyi ShiNational Key Laboratory of Lead Druggability Research, Shanghai Institute of Pharmaceutical Industry, China State Institute of Pharmaceutical Industry, Shanghai, 201203, China.
Weidong ZhangNational Key Laboratory of Lead Druggability Research, Shanghai Institute of Pharmaceutical Industry, China State Institute of Pharmaceutical Industry, Shanghai, 201203, China. wdzhangy@hotmail.com.
Qingyan SunNational Key Laboratory of Lead Druggability Research, Shanghai Institute of Pharmaceutical Industry, China State Institute of Pharmaceutical Industry, Shanghai, 201203, China. sqy_2000@163.com.

Funding

Chinese Academy of Medical Sciences (CAMS) Innovation Fund for Medical Sciences 2023-I2M-3-009National Key Laboratory of Lead Druggability Research NKLYT2023010National Key Research and Development Program of China 2022YFC3502000National Natural Science Foundation of China 82430119Shanghai Municipal Science and Technology Major Project ZD2021CY001the ability establishment of sustainable use for valuable Chinese medicine resources 2060302
6 · The paper itself

Abstract

The molecular volume, surface area, and polar molecular surface area are important descriptors for characterizing and predicting the molecular properties of lead compounds. Existing computational tools for calculating the above parameters often have complex workflows and are not well-suited for high-throughput conditions. CalVSP is an open-source software for computing molecular volume, molecular surface area, and polar surface area. The software implements a grid-based algorithm that dynamically optimizes grid spacing via quantum chemical reference data to ensure precise parameter calculations. CalVSP was tested on 9489 3D molecular structures, and the results revealed a mean absolute percentage error of 1.25% (95% CI: 1.23-1.27%) for the molecular volume and 1.33% (95% CI: 1.31-1.35%) for the molecular surface area compared with the quantum chemical data. For the molecular polar surface area calculations, the mean absolute percentage error was 4.59% (95% CI: 4.16-5.04%) across the 388 tested molecular structures. The CalVSP written in the C programming language offers a lightweight and easy tool. It can be integrated with other molecular property prediction tools to increase computational accuracy and for large-scale molecular calculations.

Indexed as

Computer programsMolecular surface areaMolecular volumePSA

Identifiers

PMID41462364
PMCPMC12752003

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.