Ce-224535

Ce-224535

SCHEMBL3475321

COC[C@H](O)Cn1c(=O)cnn(-c2ccc(Cl)c(C(=O)NCC3(O)CCCCCC3)c2)c1=O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

P2RX7

The experimentally established mechanism targets of Ce-224535. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 1)

geneUniProtsupporting neighboursconfidence
P2RX7 known ✓ Q99572 20/20 1.00

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Ce-224535 SCHEMBL3473554 1.00 P2RX7 (1.00) P2RX7
SCHEMBL13433834 1.00 P2RX7 (1.00) P2RX7
SCHEMBL3473601 1.00 P2RX7 (1.00) P2RX7
Ce-224535 SCHEMBL3473047 1.00 P2RX7 (1.00) P2RX7
SCHEMBL13433833 1.00 P2RX7 (1.00) P2RX7
Ce-224535 SCHEMBL31722367 1.00 P2RX7 (1.00) P2RX7
SCHEMBL3475207 1.00 P2RX7 (1.00) P2RX7
SCHEMBL3472374 0.99 P2RX7 (0.98) P2RX7
SCHEMBL13433836 0.99 P2RX7 (0.98) P2RX7
SCHEMBL13433835 0.99 P2RX7 (0.98) P2RX7

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 148 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4680203-A1 COMPOSITIONS FOR SUSTAINED RELEASE OF POORLY SOLUBLE ACTIVE INGREDIENTS Prolevi Bio AB (SE) 2026-01-21 EP claimed
WO-2025229484-A1 PURINERGIC P2 RECEPTOR ANTAGONISTS FOR USE IN THE TREATMENT OF CONGENITAL SIDEROBLASTIC ANEMIAS UNIVERSITÀ DEGLI STUDI DI BARI ALDO MORO (IT) 2025-11-06 WO claimed
US-20250129093-A1 COMPOSITIONS AND METHODS RELATING TO ATP/P2X7R SIGNALING INHIBITION THE CHILDREN'S MEDICAL CENTER CORPORATION (US) 2025-04-24 US claimed
EP-4479366-A2 COMPOSITIONS AND METHODS RELATING TO ATP/P2X7R SIGNALING INHIBITION The Children's Medical Center Corporation (US) 2024-12-25 EP claimed
WO-2024189127-A1 COMPOSITIONS FOR SUSTAINED RELEASE OF POORLY SOLUBLE ACTIVE INGREDIENTS PROLEVI BIO AB (SE) 2024-09-19 WO claimed
WO-2023158601-A2 COMPOSITIONS AND METHODS RELATING TO ATP/P2X7R SIGNALING INHIBITION THE CHILDREN'S MEDICAL CENTER CORPORATION (US) 2023-08-24 WO claimed
EP-4157288-A2 MODULATORS OF PURINERGIC RECEPTORS AND RELATED IMMUNE CHECKPOINT FOR TREATING ACUTE RESPIRATORY DISTRESS SYNDROM Institut Gustave-Roussy (FR) 2023-04-05 EP claimed
US-7671053-B2 Benzamide inhibitors of the P2X7 receptor PFIZER, INC. (US) 2010-03-02 US claimed
EP-1776352-A1 METHOD FOR PREPARING 5-[4-(2-HYDROXY-PROPYL)-3,5-DIOXO-4,5-DIHYDRO-3H[1,2,4]TRIAZIN-2-YL]-BENZAMIDE DERIVATIVES BY DEPROTECTING THE HYDROXYL-PROTECTED PRECURSERS Pfizer Products Inc. (US) 2007-04-25 EP claimed
EP-1768965-A1 METHOD FOR PREPARING 5-¬4-(2-HYDROXY-ETHYL)-3,5-DIOXO-4,5-DIHYDRO-3H-¬1,2,4|-TRIAZIN-2-YL|BENZAMIDE DERIVATIVES WITH P2X7 INHIBITING ACTIVITY BY REACTION OF THE DERIVATIVE UNSUBSTITUTED IN 4-POSITION OF THE TRIAZINE WITH AN OXIRAN IN THE PRESENCE OF A LEWIS ACID Pfizer Products Incorporated (US) 2007-04-04 EP claimed
WO-2006003500-A1 METHOD FOR PREPARING 5-`4-(2-HYDROXY-PROPYL)-3,5-DIOXO-4,5-DIHYDRO-3H`1,2,4!TRIAZIN-2-YL!-BENZAMIDE DERIVATIVES BY DEPROTECTING THE HYDROXYL-PROTECTED PRECURSERS PFIZER PRODUCTS INC. (US) 2006-01-12 WO claimed
WO-2006003513-A1 METHOD FOR PREPARING 5-`4-(2-HYDROXY-ETHYL)-3,5-DIOXO-4,5-DIHYDRO-3H-`1,2,4!-TRIAZIN-2-YL!BENZAMIDE DERIVATIVES WITH P2X7 INHIBITING ACTIVITY BY REACTION OF THE DERIVATIVE UNSUBSTITUTED IN 4-POSITION OF THE TRIAZINE WITH AN OXIRAN IN THE PRESENCE OF A LEWIS ACID PFIZER PRODUCTS INC. (US) 2006-01-12 WO claimed
US-20050288256-A1 Methods for preparing P2X7 inhibitors PFIZER INC. 2005-12-29 US claimed
US-20050288288-A1 Methods for preparing P2X7 inhibitors PFIZER INC. 2005-12-29 US claimed
US-6974812-B2 Benzamide inhibitors of the P2X7 Ereceptor PFIZER INC. (US) 2005-12-13 US claimed
US-20260144674-A1 Apparatus and Methods for Drug Delivery Using Microneedles CLEARSIDE BIOMEDICAL, INC. (US) 2026-05-28 US disclosed
US-12599664-B2 Pharmaceutical products and stable liquid compositions of IL-17 antibodies NOVARTIS AG (CH) 2026-04-14 US disclosed
US-20050288256-A1 Methods for preparing P2X7 inhibitors PFIZER INC. 2005-12-29 US disclosed
US-20050288288-A1 Methods for preparing P2X7 inhibitors PFIZER INC. 2005-12-29 US disclosed
US-20050288288-A1 Methods for preparing P2X7 inhibitors PFIZER INC. 2005-12-29 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (5 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-12599664-B2 Pharmaceutical products and stable liquid compositions of IL-17 antibodies IL17A, IL15, IL5 P2RX7 313/4885
US-20260144674-A1 Apparatus and Methods for Drug Delivery Using Microneedles PROKR2, SLC10A2, GLP1R P2RX7 2434/4885
US-20250129093-A1 COMPOSITIONS AND METHODS RELATING TO ATP/P2X7R SIGNALING INHIBITION P2RY1, P2RX3, P2RX1 P2RX7 4/4885
US-20050288256-A1 Methods for preparing P2X7 inhibitors P2RX7, P2RX1, P2RX3 P2RX7 1/4885
US-20050288288-A1 Methods for preparing P2X7 inhibitors P2RX7, P2RX1, P2RX2 P2RX7 1/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.