ACD/Labs' physicochemical, ADME-Tox, and structure modification models and algorithms—industry-standard for computational and medicinal chemists for over two decades—are available as a web application. The portal offers an off-the-shelf browser-based solution for deployment of Percepta property prediction and decision-making tools and a fully supported alternative to organizations seeking to replace in-house prediction dashboards.
ACD/Percepta Portal for Scientists
ACD/Percepta Portal delivers the algorithms and models you've come to depend on, in a web-based platform that both you and your IT team can get behind.
Where and When You Want
ACD/Labs' industry standard models are brought to your fingertips via the browser of any computer or tablet connected to the company's network. With project files and other data stored centrally you are no longer limited to a particular operating system or device.
ACD/Percepta Portal delivers full prediction modules for LogD, LogP, and pKa. It also provides predicted values (in the Spreadsheet, Profiling, Plotting, and Structure Design workspaces) for the models listed below:
The Absolv prediction module calculates Abraham solvation parameters and is the result of collaboration between ACD/Labs and Prof. M. H. Abraham—the original author of this six parameter system.
- A—Hydrogen bonding acidity
- B and B0—Hydrogen bonding basicity parameters
- L—Partitioning coefficient between gas phase and hexadecane
- V—McGowan volume
- E—Excessive molar refraction
Read complete information about ACD/Absolv
Aqueous (Water) Solubility Module
- Calculates pH dependent aqueous solubility, intrinsic solubility, and solubility of the chemical dissolved in pure (unbuffered) water at 25°C and zero ionic strength; along with the equilibrium pH of the solution
- The model is trainable with experimental values to improve predictions for proprietary chemical space
Boiling Point/Vapor Pressure Module
- Estimates the boiling point of organic compounds at specified pressure
- Predicts the vapor pressure of organic compounds as a function of temperature
The distribution coefficient, D, is a pH dependant measure of the propensity of a molecule to differentially dissolve in two immiscible phases, taking into account all ionized and unionized forms (microspecies). It serves as a quantitative descriptor of lipophilicity. The ACD/LogD prediction module provides the following possibilities:
- Estimate the value of the octanol-water distribution constant, as the logarithmic ratio (logD), from structure at any pH (0–14)
- Adapt the model to proprietary chemical spaces by training the underlying logP or pKa prediction algorithms
Read complete information about ACD/LogD
The partition constant, P, is a measure of the propensity of a neutral molecule to differentially dissolve in two immiscible phases, and serves as a quantitative descriptor of lipophilicity. The logP prediction model provides an estimate of the value of the octanol-water partitioning coefficient (also referred to as KOW) as the logarithmic ratio (logP), from structure.
LogP predictions are exploited as input variable in many of our PhysChem and ADME prediction algorithms including logD, Oral Bioavailability, Blood-Brain Barrier Permeation, Passive Absorption, and several Toxicity models, such as hERG inhibition and Aquatic toxicity.
Read complete information about ACD/LogP
The acid dissociation constant, Ka, is a measure of the tendency of a molecule or ion to keep a proton (H+) at its ionization center(s). It is related to the ionization ability of a chemical species and is a core property that defines chemical and biological behaviour. The pKa prediction model from ACD/Labs offers the following functionality:
- Calculation of accurate acid and base pKa constants (pKa = -logKa) under standard conditions (25°C and zero ionic strength) in aqueous solutions for every ionizable group within organic structures
- Confidence intervals for all predicted pKa values, indicating their accuracy
Read complete information about ACD/pKa
- A model for calculation of substituent-specific parameters for selected fragments of the molecule:
- Eectronic constants (Hammett Sigmas)
- Steric constants (molar volume, molar refractivity)
- Hydrophobic constant (Hansch Pi)
Other PhysChem Descriptors
The models are available for the estimation for the following basic physicochemical properties:
- Freely Rotatable Bonds
- H-Bond Donors and Acceptors
- Index of Refraction
- Molar Refractivity
- Molar Volume
- Molecular Weight
- Polar Surface Area
- Surface Tension
Blood Brain Barrier Permeation Module
The blood-brain barrier (BBB) permeation model in ACD/Labs software provides a comprehensive evaluation of the permeation potential of candidate compounds. While prediction cannot replace experimentation, this module allows compounds to be ranked according to their passive transport across the BBB, based on the following information:
- Predictions of:
- Rate of passive diffusion/permeability (logPS)
- Extent of BBB permeation (logBB)—steady-state distribution ratio of a compound between brain tissue and plasma
- Brain/plasma equilibration rate (PS * fu, brain)
- Alerts for compounds likely to undergo transport across the BBB barrier by carrier mediated mechanisms
Read complete information about ACD/Blood Brain Barrier
Cytochrome P450 Inhibitors Module
- Calculates the probability that your compound will be an inhibitor of one of the five major drug metabolizing enzymes—CYP3A4, CYP2D6, CYP2C9, CYP2C19, and CYP1A2—at two different IC50 thresholds
- IC50 < 50 µM (general inhibition);
- IC50 < 10 µM (efficient inhibition)
- The model can be trained with experimental data for new compounds in order to expand its applicability domain
Cytochrome P450 Substrates Module
- Calculates the probability that your compound will be a substrate of one of the five major drug metabolizing enzymes—CYP3A4, CYP2D6, CYP2C9, CYP2C19, and CYP1A2
- The model can be trained with experimental data for new compounds in order to expand its applicability domain
- Estimates the strength of drug binding to human plasma proteins as either the overall percentage bound in plasma or as an affinity constant to human serum albumin
- Both the %PPB and logKa(HSA) models are trainable with user data
- Predict their apparent volume of distribution (Vd)
Maximum Recommended Daily Dose Module
- Approximate an estimation of the maximum oral dose of drug that can be used in the clinic
Oral Bioavailability Module
The oral bioavailability model uses a combination of probabilistic and mechanistic modeling techniques to predict oral bioavailability from structure, and relies on a number of other ACD/Labs prediction algorithms and experimental data sets. Results are provided as a quantitative prediction of bioavailability after oral administration (%F) of a dose defined by the user.
- Predict a number of endpoints that affect oral bioavailability:
- Solubility (dose/solubility ratio)
- Stability in acidic media
- Intestinal membrane permeability by passive or active transport (with a summary of transporters where relevant)
- P-gp efflux
- First pass metabolism in the liver
- View up to 5 of the most similar structures from the internal training set, with experimental results and literature references
Read complete information about ACD/Oral Bioavailability
Passive Absorption Module
Human Intestinal Absorption (HIA) and solubility are two key factors that affect oral bioavailability. The Passive Absorption model predicts the human intestinal permeability of drugs, taking into account trans-cellular and para-cellular routes, and ionization-specific differences in permeation rates. Predictions are based on mechanistic models that use a number of physicochemical parameters, including lipophilicity and ionization, as inputs. The model outputs the following calculated parameters:
- The extent of Human Intestinal Absorption (HIA) in terms of passive transport across the intestine(not affected by any side processes such as limited solubility/dissolution, variable oral dose, chemical stability, active transport, and first pass metabolism in gut or liver), indicating percentage contribution from transcellular and paracellular route.
- Passive permeability across jejunal epithelium, also indicating absorption rate.
- Passive permeability across Caco-2 cell monolayers, indicating percentage contribution from transcellular and paracellular route.
Read complete information about ACD/Passive Absorption
P-gp Specificity Module
P-glycoprotein (P-gp) is a clinically relevant efflux transporter that extrudes compounds from a large variety of cells. Its function has been associated with the drugs' absorption, distribution, excretion, CNS effects, multidrug resistance (MDR). P-gp transports a variety of natural compounds and drugs of different therapeutic areas.
Rapid identification of drug candidates that are P-gp substrates and/or inhibitors is possible using P-gp specificity model. Filtering and exclusion of P-gp substrates/inhibitors from huge ‘in-house' libraries of synthesized compounds or virtual libraries is possible, followed by exclusion of such compounds from further development. P-gp specificity model may serve as an initial screen that could replace screening test based on P-gp ATPase activity measurements and partially replace expensive experiments with P-gp expressing cell monolayers and P-gp knock-out animals.
PK Explorer Module
- Estimates a number of parameters determining the pharmacokinetic profile of your compounds by using a set of differential equations from a multi-compartment model describing the organism of an average statistical human:
- Tmax and Cp(max)
- AUC after oral and intravenous administrations
- Oral Bioavailability
Acute Toxicity Module
- Predicts quantitative LD50 values for two rodent species after different administration routes:
- LD50 in mice after oral administration
- LD50 in mice after intravenous administration
- LD50 in mice after intraperitoneal administration
- LD50 in mice after subcutaneous administration
- LD50 in rats after oral administration
- LD50 in rats after intraperitoneal administration
- Estimates qualitative OECD Hazard categories
- The expert system identifies hazardous substructures potentially responsible for the toxic effect
Aquatic Toxicity Module
- Predict LC50 values of your compounds for two aquatic organisms—fathead minnows (P. promelas) and water fleas (D. magna)
Endocrine System Disruption Module
- Predicts the relative binding affinity of your compounds to the Estrogen Receptor which is associated with the possibility of reproductive toxicity and cancers
- Provides predictions for the probability of your producing a positive Ames test outcome
Health Effects Module
- Predicts the probable adverse effects of a compound on particular organs or organ systems based on long term organ specific toxicity studies encompassing various species and routes of administration
- The following organs and organ systems are considered:
- Cardiovascular system
- Gastrointestinal system
hERG Inhibition Module
- Evaluates your compounds for cardiotoxicity related to drug interactions with the human ether-a-go-go (hERG) channel
- Calculates the potential of a compound to cause moderate or stronger eye and skin irritation as per the Draize test
†Full prediction modules (all modules offer Spreadsheet, Profiling and Structure Design Workspaces)
A number of workspaces and data visualization tools are available to aid decision-making:
- Spreadsheet Workspace*—analysis and evaluation of compounds is made easy with the ability to view predictions from ACD/Percepta, third party, and in-house algorithms and models in one screen
- Profiling Dashboard*—a fully configurable workspace for at-a-glance visualization of the information you are most interested in
- Plotting Workspace—a dedicated interface for data analysis
- Structure Design Workspace—modify chemical structures based on property requirements. The Portal version allows for enumeration of many more compounds for investigation of greater chemical space
* Individual licenses required for ACD/Percepta models.
Quickly Identify Effective compounds
Dynamic visualization of results—.structural fragment/atomic contributions provide insights to direct new projects to accelerate decision-making, and reduce trial-and-error experimentation. See the most similar structures in the database and use reliability index/probability to assess confidence in the predicted result.
Make Data-Driven Decisions With Confidence
The Percepta Portal delivers a plotting workspace including Scatter plot, pie charts, filers and a structure grid—with dynamic connectivity for real-time analysis of results. Customize the workspace to display the information you use the most in a convenient format.
Share Experience and Ideas with Ease
The Percepta Portal facilitates collaboration for colleagues within a department, at sites around the globe, and between partners.
- Auto-synchronization of data and instant updates make simultaneously working on projects with colleagues and being current with the latest data simple (e.g., model training files, in-house algorithms etc.)
- Share the full project data in a native format for interactive analysis and re-use by others
Interested In Seeing It For Yourself?
ACD/Percepta Portal for IT Professionals
Give Scientists What They Want While Streamlining Your Efforts
Percepta portal offers easy deployment and maintenance of the algorithms and models used by computational chemists in R&D research for almost two decades.
The Server components of ACD/Percepta Portal are installed, maintained and updated in a single location (either physical or virtual) providing easy support for system administrators and IT teams. Alternatively, the entire setup can be hosted in a Cloud environment.
The web browser performs the role of the ACD/Percepta Portal Client so no additional effort is needed to deploy/maintain the software on the computers of individual users.
V6 and above
V10 and above
Speed and Performance
Optimize the speed and performance of your system based on the available hardware and IT set-up in your organization:
- Distribute computational tasks between several physical/virtual machines
- Modify the pool of available calculation kernels in real-time, depending on the workload
Integrate Into Your Existing IT Landscape
The ACD/Percepta Portal Application Programming Interface (API) provides extensive options for integration of this product into an existing IT landscape:
- Communication with corporate Databases, existing in-house web Portals, etc. can be implemented
- Product architecture allows for an integration of in-house predictive algorithms into ACD/Percepta Portal and vice versa
- Expansion of existing in-house web applications with ACD/Percepta Portal interface widgets is a potential option
The need for a Windows OS component on the server side will be eliminated in continuing development.
Minimum System Requirements