How COVALfinder® assays work
COVALfinder® is a highly tuned and optimized TR-FRET Binding Kinetic Assay based on the binding and displacement of an active-site directed fluorescent probe.
Real-time binding of the fluorescent probe is detected using a labeled anti-tag antibody, which binds to the target of interest. The binding of the fluorescent probe and labeled antibody to the target increases the TR-FRET signal, whereas the displacement of the fluorescent probe with a compound decreases the TR-FRET signal.
To ensure that our kinetic assays consistently deliver the highest quality data we always introduce up to 48 controls and a reference compound in each analysis.
Our services

Inactivation Kinetics
COVALfinder® is a robust kinetic platform that delivers all key inactivation (kinact, kinact/KI, T1/2∞) and affinity (KI) parameters for irreversible binders.
Binding Mechanism
COVALfinder® discriminates between reversible and irreversible drugs, providing mechanism of binding and all key kinetic and affinity parameters that define the drug-target interaction.
Applications
- Easier decision-making: Ideal hit-to-lead and lead optimization tool to rank and develop promising irreversible compounds or reversible compounds that trigger conformational changes in the target.
- Selectivity profiling for irreversible drugs: Evaluating inactivation efficiency (kinact/KI) accurately defines the time-dependent effects of covalent binding and enables the safety profile of irreversible drugs to be more rigorously assessed.
- Discrimination between irreversible and reversible compounds. Our assays enable a detailed mechanistic characterization of the drug-target interaction. We determine whether the compound reacts reversibly or irreversibly with the target via a one- or two-step mechanism.
- Build better models: PK/PD models that integrate kinetics better predict target engagement, drug dose and treatment schedule.
Features and benefits
Reliable and accurate: Kinetic and affinity parameters are precise regardless of magnitude. In depth studies demonstrate concordance with literature values.
There is a very good correlation between the kinact, KI and kinact/KI values of thirteen irreversible inhibitors with five different targets obtained from our assays and those obtained from activity assays reported in the literature1-8. Moreover, our assays provide accurate results regardless of the magnitude of the value measured.
COVALfinder® | References | ||||||||
Compound | Target |
KI (nM) |
Kinact (s-1) |
Kinact/KI (M-1 s-1) |
T1/2∞ (min) |
KI (nM) |
Kinact (s-1) |
Kinact/KI (M-1 s-1) |
T1/2∞ (min) |
Ibrutinib | BTK | 37 |
1.0×10-2 |
2.7×105 |
1 | 54 |
2.7×10-2 |
4.8×105 |
0.4 |
Acalabrutinib | 164 |
4.8×10-3 |
2.9×104 |
2 | 181 |
5.6×10-3 |
3.1×104 |
2 | |
THZ1 | CDK7/Cyc H/MNAT1 | 143 |
1.4×10-3 |
9.8×103 |
8 | 255 |
7.7×10-4 |
3.0×103 |
15 |
SY1365 | 33 |
1.1×10-3 |
3.8×104 |
10 | 17 |
2.3×10-3 |
8.0×104 |
5 | |
THZ531 | CDK12/Cyc K | 81 |
1.1×10-3 |
1.3×104 |
10 | 82 |
3.5×10-3 |
4.3×104 |
3 |
PRN1371 | FGFR1 | 23 |
2.7×10-2 |
4.4×105 |
0.4 | 1.6 |
1.9×10-3 |
1.2×106 |
6 |
Osimertinib | EGFR | 15 |
8.2×1-3 |
5.5×105 |
1 | 14 |
7.2×10-3 |
5.3×105 |
2 |
Dacomitinib | 0.24 |
3.8×10-3 |
1.6×107 |
3 | 0.16 |
1.5×10-3 |
9.9×106 |
11 | |
Neratinib | 1.21 |
5.3×10-3 |
4.4×106 |
2 | 7.1 |
1.8×10-3 |
2.5×105 |
9 | |
Afatinib | 0.13 |
6.0×10-3 |
4.6×107 |
2 | 0.15 |
9.0×10-4 |
6.3×106 |
19 | |
Canertinib | 0.64 |
6.0×10-3 |
9.5×106 |
3 | 0.093 |
2.9×10-3 |
2.3×107 |
6 | |
Nazartinib | 60 |
6.2×10-3 |
1.0×105 |
2 | 25 |
5.2×10-3 |
2.1×105 |
3 | |
Poziotinib | 0.60 |
9.1×10-3 |
1.5×107 |
1 | <1 |
8.3×10-4 |
>1.2×106 |
20 |

We are experts in kinetic profiling
Enzymlogic is a world leading analytical CRO, expert in generation and interpretation of kinetic data. We are proud to serve the smallest biotech innovators through to 8 of the world’s top 20 Pharma organizations, supporting drug hunters in their search for the most promising compounds in early discovery.
References
- Barf T. et al. (2017) J Pharmacol Exp Ther. 363(2):240-252.
- Kwiatkowski N. et al. (2014) Nature. 511(7511):616-20.
- Shanhu Hu S. et al. (2019) Cancer Res. 79(13):3479-3491.
- Zhang T. et al (2016) Nat Chem Biol. 12(10):876-84.
- Bradley M. et al. (2017) AACR Annual Meeting.
- Lategahn J. et al. (2019) Chem Sci. 10(46):10789-10801.
- Schwartz P.A. et al. (2014) Proc Natl Acad Sci U S A. 111(1):173-8.
- Fassunke J. et al. (2018) Nat Commun. 9(1):4655.
Sensitive: Our flexible and highly sensitive assays enable the identification and discrimination of a wide spectrum of compounds.
COVALfinder® is a flexible and highly sensitive platform that uses low protein concentrations (from picomolar to low nanomolar), precise TR-FRET readouts and continuous measurements that enables the identification and discrimination of a wide spectrum of compounds:
- Slow to rapid binders
- Weak to potent binders.
Robust and reproducible: Our assays show outstanding robustness and reproducibility between plates and days.
The high and sustained stability of our assays guarantees reproducible and robust results over time.
- Outstanding reproducibility between plates and days.
- Enables data to be interpreted with confidence.
- High Z-values ensure low false positive/negative rates.
Our assays ensure robust measurement over time


Our assays are highly reproducible between plates and days
Figure 4. COVALfinder® provides outstanding reproducibility between plates and days. Profiling of a reversible reference compound against 1 target over a six-month period. Analysis of the affinity (Kd) and kinetic constants (k1, k2) taken from 3 different compound, enzyme, probe and antibody lots demonstrate less than 5-fold variance.
Rapid turnaround and cost effective: We are committed to delivering rapid and reliable data turnaround, on time and to budget, helping you keep your programs on track.
Quality data, delivered on schedule
We are laser focused on rapid and reliable data delivery, with a keen eye on timelines and budgets.
- Standard data turnaround for study requests is 10 business days from compound receipt.
- Expedited turnaround is available for regularly scheduled ongoing screening programs.
We offer flexible solutions
Together we will define the best way to collaborate through:
- Ready-to-use or user-defined assays.
- User-defined screening concentrations.
- Bespoke assay development.
- Flexible service models to support your discovery goals and maximize program success rates.
- Direct contract, sub-contract via your principal CRO service provider or using outsourcing services (including Scientist and Science Exchange).
List of targets ready to use
Our expertise extends beyond kinases to GPCR and other target types.
Search our database to discover whether your target is:- May be possible: We have a strong track record of achievement where others fail! Contact us to find out more.
- Clear line of sight: Establishment requires finalization / validation, which typically takes 2-4 weeks to complete.
- Good to go: Data within 2 weeks of compound receipt.
* Full length and partial length forms are available.
Target name | Alternative names | KINETICfinder | COVALfinder |
---|---|---|---|
ALK | ALK, CD246, NBLST3 | Good to go | May be possible |
ALK1 (ACVRL1) | ALK1, ALK-1, ACVRLK1, HHT, HHT2, ORW2, SKR3, TSR-I | Good to go | May be possible |
ARAF | A-RAF, ARAF1, PKS2, RAFA1 | Good to go | Good to go |
AXL | JTK11, UFO | Good to go | May be possible |
BLK | MODY11 | Good to go | May be possible |
BRAF V600E | B-RAF1, B-raf, BRAF1, NS7, RAFB1 | Good to go | Good to go |
BRAF* | B-RAF1, B-raf, BRAF1, NS7, RAFB1 | Good to go | Good to go |
BTK (activated) | AGMX1, AT, ATK, BPK, IGHD3, IMD1, PSCTK1, XLA | Good to go | Good to go |
BTK (non-activated) | AGMX1, AT, ATK, BPK, IGHD3, IMD1, PSCTK1, XLA | Good to go | Good to go |
CDK1/cyclin B | CDC2, CDC28A, P34CDC2 | Good to go | Good to go |
CDK12/cyclin K | CRK7, CRKR, CRKRS | Good to go | Good to go |
CDK13/cyclin K | CDC2L, CDC2L5, CHDFIDD, CHED, hCDK13 | Good to go | May be possible |
CDK16/cyclin Y | PCTK1, PCTAIRE, PCTAIRE1, PCTGAIRE, | Good to go | May be possible |
CDK7/cyclin H/MNAT | CAK, CAK1, CDKN7, HCAK, MO15, STK1, p39MO15 | Good to go | Good to go |
CDK9/cyclin T1 | C-2k, CDC2L4, CTK1, PITALRE, TAK | Good to go | Good to go |
CHEK2 (CHK2) | CHK2, CDS1, HuCds1, LFS2, PP1425, RAD53, hCds1 | Good to go | May be possible |
CK1e (CSNK1E) | CKIe, CKIepsilon, HCKIE | Good to go | May be possible |
CLK2 | CDC like kinase 2 | Good to go | May be possible |
CRAF (RAF1) | CMD1NN, CRAF, NS5, Raf-1, c-Raf | Good to go | Good to go |
CSF1R (FMS) | FMS, BANDDOS, C-FMS, CD115, CSF-1R, CSFR, FIM2, HDLS, HDLS1, M-CSF-R | Good to go | May be possible |

How can we help?
Our experienced project manager will work with you to identify the best way forward for your project.