Azd-8797

Azd-8797

SCHEMBL213194

CC(C)C[C@H](CO)Nc1nc(S[C@@H](C)c2ccccc2)nc2nc(N)sc12

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
CX3CR1 P49238 20/20 1.00
CXCR2 P25025 18/20 1.00
ADORA1 P30542 1/20 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
Azd-8797 SCHEMBL29473543 1.00 CX3CR1 (1.00) CX3CR1CXCR2ADORA1
Azd-8797 SCHEMBL30914115 1.00 CX3CR1 (1.00) CX3CR1CXCR2ADORA1
Azd-8797 SCHEMBL212862 1.00 CX3CR1 (1.00) CX3CR1CXCR2ADORA1
Azd-8797 SCHEMBL212398 1.00 CX3CR1 (1.00) CX3CR1CXCR2ADORA1
Azd-8797 SCHEMBL30914151 1.00 CX3CR1 (1.00) CX3CR1CXCR2ADORA1
Azd-8797 SCHEMBL23528828 1.00 CX3CR1 (1.00) CX3CR1CXCR2ADORA1
Azd-8797 SCHEMBL31643602 1.00 CX3CR1 (1.00) CX3CR1CXCR2ADORA1
Azd-8797 SCHEMBL23828002 0.99 CX3CR1 (0.98) CX3CR1CXCR2ADORA1
Azd-8797 SCHEMBL23828005 0.99 CX3CR1 (0.98) CX3CR1CXCR2ADORA1
Azd-8797 SCHEMBL30288320 0.99 CX3CR1 (0.98) CX3CR1CXCR2ADORA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250195549-A1 NEW USE KANCERA AB (SE) 2025-06-19 US claimed
US-20250195548-A1 NEW USE KANCERA AB (SE) 2025-06-19 US claimed
US-20230068240-A1 A Process for the Steroselective Preparation of Chiral 2-[(Hetero)Arylalkylsulfanyl]Pyrimidines and Products Obtainable Therefrom KANCERA AB (SE) 2023-03-02 US claimed
US-20210188873-A1 A Process for the Steroselective Preparation of Chiral 2-[(Hetero)Arylalkylsulfanyl]Pyrimidines and Products Obtainable Therefrom KANCERA AB (SE) 2021-06-24 US claimed
US-9440992-B2 5,7-disubstituted thiazolo[4,5-D]pyrimidines as chemokine inhibitors Acturum Life Science AB (SE) 2016-09-13 US claimed
US-7947693-B2 2R)-2-[(2-amino-5-{[(1S)-1-(2-fluorophenyl)ethyl]thio}[1,3]thiazolo[4,5-d]pyrimidin-7-yl)amino]pentan-1-ol; neurodegenerative disorders, demyelinating disease, cardio- and cerebrovascular atherosclerotic disorders, peripheral artery disease, rheumatoid arthritis, pulmonary diseases su COPD, asthma ASTRAZENECA AB (SE) 2011-05-24 US claimed
US-20110092519-A1 5,7-DISUBSTITUTED THIAZOLO[4,5-D]PYRIMIDINES AS CHEMOKINE INHIBITORS ASTRAZENECA AB (SE) 2011-04-21 US claimed
EP-1869056-B1 NOVEL 5-SUBSTITUTED 7-AMINO-Ý1,3¨THIAZOLOÝ4,5-D¨PYRIMIDINE DERIVATIVES ASTRAZENECA AB (SE) 2010-11-10 EP claimed
US-20080214578-A1 Novel 5-Substituted 7-Amino-[1,3]Thiazolo[4,5-D]Pyrimidine Derivatives 793 ACTURUM REAL ESTATE AB (SE) 2008-09-04 US claimed
US-20250230170-A1 Process for the Steroselective Preparation of Chiral 2-[(Hetero)Arylalkylsulfanyl]Pyrimidines and Products Obtainable Therefrom KANCERA AB (SE) 2025-07-17 US disclosed
US-20250195548-A1 NEW USE KANCERA AB (SE) 2025-06-19 US disclosed
US-20250195549-A1 NEW USE KANCERA AB (SE) 2025-06-19 US disclosed
US-12264165-B2 Process for the stereoselective preparation of chiral 2-[(hetero) arylalkylsulfanyl]pyrimidines and products obtainable therefrom KANCERA AB (SE) 2025-04-01 US disclosed
US-12060380-B2 Phosphate and phosphonate derivatives of 7-amino-5-thio-thiazolo[4,5-d]pyrimidines and their use in treating conditions associated with elevated levels of CX3CR1 and/or CX3CL1 KANCERA AB (SE) 2024-08-13 US disclosed
US-8088780-B2 5,7-disubstituted thiazolo[4,5-D]pyrimidines for the selective inhibition of chemokine receptors ASTRAZENECA AB (SE) 2012-01-03 US disclosed
US-7947693-B2 2R)-2-[(2-amino-5-{[(1S)-1-(2-fluorophenyl)ethyl]thio}[1,3]thiazolo[4,5-d]pyrimidin-7-yl)amino]pentan-1-ol; neurodegenerative disorders, demyelinating disease, cardio- and cerebrovascular atherosclerotic disorders, peripheral artery disease, rheumatoid arthritis, pulmonary diseases su COPD, asthma ASTRAZENECA AB (SE) 2011-05-24 US disclosed
US-20110092519-A1 5,7-DISUBSTITUTED THIAZOLO[4,5-D]PYRIMIDINES AS CHEMOKINE INHIBITORS ASTRAZENECA AB (SE) 2011-04-21 US disclosed
EP-1869056-B1 NOVEL 5-SUBSTITUTED 7-AMINO-Ý1,3¨THIAZOLOÝ4,5-D¨PYRIMIDINE DERIVATIVES ASTRAZENECA AB (SE) 2010-11-10 EP disclosed
US-20090124637-A1 Novel 5,7-Disubstituted [1,3]Thiazolo[4,5-D]Pyrimidin-2(3H)-One Derivatives 794 ASTRAZENECA AB (SE) 2009-05-14 US disclosed
US-20080214578-A1 Novel 5-Substituted 7-Amino-[1,3]Thiazolo[4,5-D]Pyrimidine Derivatives 793 ACTURUM REAL ESTATE AB (SE) 2008-09-04 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 (10 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-20110092519-A1 5,7-DISUBSTITUTED THIAZOLO[4,5-D]PYRIMIDINES AS CHEMOKINE INHIBITORS CX3CR1, CCR2, CXCR3 CX3CR1 1/4885CXCR2 6/4885ADORA1 60/4885
US-12264165-B2 Process for the stereoselective preparation of chiral 2-[(hetero) arylalkylsulfanyl]pyrimidines and products obtainable therefrom CYP2B6, CYP2S1, CYP2D6 CX3CR1 1795/4885CXCR2 430/4885ADORA1 170/4885
US-20210188873-A1 A Process for the Steroselective Preparation of Chiral 2-[(Hetero)Arylalkylsulfanyl]Pyrimidines and Products Obtainable Therefrom CYP2S1, CYP2B6, TYMS CX3CR1 3509/4885CXCR2 1602/4885ADORA1 278/4885
US-12060380-B2 Phosphate and phosphonate derivatives of 7-amino-5-thio-thiazolo[4,5-d]pyrimidines and their use in treating conditions associated with elevated levels of CX3CR1 and/or CX3CL1 CX3CR1, CXCR3, CXCR1 CX3CR1 1/4885CXCR2 16/4885ADORA1 49/4885
US-20230068240-A1 A Process for the Steroselective Preparation of Chiral 2-[(Hetero)Arylalkylsulfanyl]Pyrimidines and Products Obtainable Therefrom CYP2S1, CYP2B6, TYMS CX3CR1 3509/4885CXCR2 1602/4885ADORA1 278/4885
US-20080214578-A1 Novel 5-Substituted 7-Amino-[1,3]Thiazolo[4,5-D]Pyrimidine Derivatives 793 CX3CR1, CCR2, CXCR3 CX3CR1 1/4885CXCR2 11/4885ADORA1 69/4885
US-20250230170-A1 Process for the Steroselective Preparation of Chiral 2-[(Hetero)Arylalkylsulfanyl]Pyrimidines and Products Obtainable Therefrom CYP2S1, CYP2B6, CYP2F1 CX3CR1 3602/4885CXCR2 1814/4885ADORA1 367/4885
US-20250195548-A1 NEW USE F12, TNNI3, SERPINC1 CX3CR1 703/4885CXCR2 441/4885ADORA1 868/4885
US-20250195549-A1 NEW USE F12, TNNI3, SERPINC1 CX3CR1 703/4885CXCR2 441/4885ADORA1 868/4885
US-20090124637-A1 Novel 5,7-Disubstituted [1,3]Thiazolo[4,5-D]Pyrimidin-2(3H)-One Derivatives 794 CX3CR1, CCR2, CCR5 CX3CR1 1/4885CXCR2 5/4885ADORA1 85/4885

“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.