Crelosidenib

Crelosidenib

SCHEMBL20289768

C=CC(=O)N1CCN([C@H](CC2CC2)c2ccc([C@H](C)Nc3ncc4c(n3)N(CC)C(=O)OC4)cc2)CC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 2)

geneUniProtsupporting neighboursconfidence
▸ IDH1 O75874 20/20 1.00
▸ IDH2 P48735 16/20 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
Crelosidenib SCHEMBL29765374 1.00 IDH1 (1.00) IDH1IDH2
Crelosidenib SCHEMBL20270338 1.00 IDH1 (1.00) IDH1IDH2
Crelosidenib SCHEMBL20270341 1.00 IDH1 (1.00) IDH1IDH2
Crelosidenib SCHEMBL29427547 1.00 IDH1 (1.00) IDH1IDH2
Crelosidenib SCHEMBL20271764 1.00 IDH1 (1.00) IDH1IDH2
Crelosidenib SCHEMBL21799142 0.97 IDH1 (0.94) IDH1IDH2
SCHEMBL24170447 0.97 IDH1 (0.94) IDH1IDH2
SCHEMBL24170446 0.97 IDH1 (0.94) IDH1IDH2
SCHEMBL24170089 0.97 IDH1 (0.94) IDH1IDH2
SCHEMBL25227127 0.97 IDH1 (0.94) IDH1IDH2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240261294-A1 METHOD FOR TREATING IDH INHIBITOR-RESISTANT SUBJECTS ELI LILLY AND COMPANY 2024-08-08 — — US claimed
EP-4125915-B1 COMBINATION THERAPY WITH A MUTANT IDH INHIBITOR LILLY CO ELI (US) 2024-04-17 — — EP claimed
EP-4125917-B1 COMBINATION THERAPY WITH A MUTANT IDH INHIBITOR AND A BCL-2 INHIBITOR LILLY CO ELI (US) 2024-04-17 — — EP claimed
EP-4125916-B1 METHOD FOR TREATING IDH1 INHIBITOR-RESISTANT SUBJECTS LILLY CO ELI (US) 2024-04-17 — — EP claimed
EP-4337217-A1 METHOD FOR TREATING IDH INHIBITOR-RESISTANT SUBJECTS Eli Lilly and Company (US) 2024-03-20 — — EP claimed
US-20230255973-A1 COMBINATION THERAPY WITH A MUTANT IDH1 INHIBITOR, A DEOXYADENOSINE ANALOG, AND A PLATINUM AGENT ELI LILLY AND COMPANY 2023-08-17 — — US claimed
WO-2023141087-A1 COMBINATION THERAPY WITH A MUTANT IDH INHIBITOR ELI LILLY AND COMPANY (US) 2023-07-27 — — WO claimed
US-20230146387-A1 COMBINATION THERAPY WITH A MUTANT IDH INHIBITOR ELI LILLY AND COMPANY 2023-05-11 — — US claimed
US-20230135992-A1 COMBINATION THERAPY WITH A MUTANT IDH INHIBITOR AND A BCL-2 INHIBITOR ELI LILLY AND COMPANY 2023-05-04 — — US claimed
EP-4125916-A1 METHOD FOR TREATING IDH1 INHIBITOR-RESISTANT SUBJECTS ELI LILLY AND COMPANY (US) 2023-02-08 — — EP claimed
WO-2022261279-A1 METHOD FOR TREATING IDH INHIBITOR-RESISTANT SUBJECTS ELI LILLY AND COMPANY (US) 2022-12-15 — — WO claimed
CN-115443137-A Combination therapy using a mutant IDH inhibitor and a BCL-2 inhibitor 伊莱利利公司 2022-12-06 — — CN claimed
CN-115335060-A Combination therapy with mutant IDH inhibitors 伊莱利利公司 2022-11-11 — — CN claimed
CN-115335059-A Methods for treating IDH1 inhibitor resistant subjects 伊莱利利公司 2022-11-11 — — CN claimed
CN-115109075-A Mutant IDH1 and IDH2 inhibitors 伊莱利利公司 2022-09-27 — — CN claimed
CN-110072867-B 7-phenylethylamino-4H-pyrimido [4,5-D ] [1,3] oxazin-2-one compounds as inhibitors of mutant IDH1 and IDH2 伊莱利利公司 2022-07-08 — — CN claimed
US-11001596-B2 7-phenylethylamino-4H-pyrimido[4,5-d][1,3]oxazin-2-one compounds as mutant IDH1 and IDH2 inhibitors ELI LILLY AND COMPANY (US) 2021-05-11 — — US claimed
EP-3763717-A1 PYRIDO[4,3-D][1,3]OXAZIN-2-ONE AND PYRIMIDO[4,5-D][1,3]OXAZIN-2-ONE COMPOUNDS AS MUTANT IDH1 AND IDH2 INHIBITORS ELI LILLY AND CO. (US) 2021-01-13 — — EP claimed
EP-3555105-B1 7-PHENYLETHYLAMINO-4H-PYRIMIDO[4,5-D][1,3]OXAZIN-2-ONE COMPOUNDS AS MUTANT IDH1 AND IDH2 INHIBITORS LILLY CO ELI (US) 2020-10-28 — — EP claimed
US-20200079791-A1 7-PHENYLETHYLAMINO-4H-PYRIMIDO[4,5-D][1,3]OXAZIN-2-ONE COMPOUNDS AS MUTANT IDH1 AND IDH2 INHIBITORS ELI LILLY AND COMPANY 2020-03-12 — — US claimed

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

For each of this compound's patents that has machine-readable text (6 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-20230135992-A1 COMBINATION THERAPY WITH A MUTANT IDH INHIBITOR AND A BCL-2 INHIBITOR IDH2, IDH3B, IDH3A IDH1 4/4885IDH2 1/4885
US-20240261294-A1 METHOD FOR TREATING IDH INHIBITOR-RESISTANT SUBJECTS IDH3A, IDH2, IDH3B IDH1 4/4885IDH2 2/4885
US-20230255973-A1 COMBINATION THERAPY WITH A MUTANT IDH1 INHIBITOR, A DEOXYADENOSINE ANALOG, AND A PLATINUM AGENT IDH1, IDH3B, IDH3A IDH1 1/4885IDH2 5/4885
US-20200079791-A1 7-PHENYLETHYLAMINO-4H-PYRIMIDO[4,5-D][1,3]OXAZIN-2-ONE COMPOUNDS AS MUTANT IDH1 AND IDH2 INHIBITORS IDH2, IDH1, IDH3B IDH1 2/4885IDH2 1/4885
US-11001596-B2 7-phenylethylamino-4H-pyrimido[4,5-d][1,3]oxazin-2-one compounds as mutant IDH1 and IDH2 inhibitors IDH2, IDH1, IDH3B IDH1 2/4885IDH2 1/4885
US-20230146387-A1 COMBINATION THERAPY WITH A MUTANT IDH INHIBITOR IDH3B, IDH3A, FLT3 IDH1 5/4885IDH2 4/4885

“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.

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