SCHEMBL3571209

SCHEMBL3571209

COC(=O)c1ccc2c(c1)N(C(=O)OC(C)(C)C)CC2

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HDAC1 Q13547 1/20 0.53
HDAC6 Q9UBN7 1/20 0.53
XIAP P98170 1/20 0.52
BIRC2 Q13490 1/20 0.52
CHRM4 P08173 1/20 0.51
DRD2 P14416 1/20 0.51
HTR7 P34969 1/20 0.51
UCHL1 P09936 1/20 0.47
USP30 Q70CQ3 1/20 0.47
ESR2 Q92731 1/20 0.44
NR1H2 P55055 2/20 0.43
KDM4E B2RXH2 3/20 0.43
NPC1 O15118 3/20 0.43
RAB9A P51151 2/20 0.43
SMN1; SMN2 Q16637 1/20 0.43
NPSR1 Q6W5P4 1/20 0.43
MEN1 O00255 1/20 0.43
KMT2A Q03164 1/20 0.43
ALDH1A1 P00352 2/20 0.42
ALOX15 P16050 1/20 0.42

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
SCHEMBL29940282 1.00 HDAC1 (0.53) HDAC1HDAC6XIAPBIRC2CHRM4
SCHEMBL3565263 0.93 HDAC6 (0.51) HDAC1HDAC6XIAPBIRC2CHRM4
SCHEMBL846218 0.90 HDAC1 (0.53) HDAC1HDAC6CHRM4DRD2HTR7
SCHEMBL1270523 0.87 CHRM4 (0.50) HDAC1HDAC6XIAPBIRC2CHRM4
SCHEMBL29939759 0.87 CHRM4 (0.50) HDAC1HDAC6XIAPBIRC2CHRM4
SCHEMBL23063853 0.83 HDAC1 (0.52) HDAC1HDAC6UCHL1USP30KDM4E
SCHEMBL1271119 0.83 CHRM4 (0.48) HDAC1HDAC6XIAPBIRC2CHRM4
SCHEMBL28834900 0.82 NOTUM (0.60) HDAC1HDAC6XIAPBIRC2KDM4E
SCHEMBL14230676 0.82 DRD2 (0.55) BIRC2CHRM4DRD2HTR7ESR2
SCHEMBL28320901 0.81 XIAP (0.56) XIAPBIRC2KDM4ENPC1RAB9A

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 18 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4313292-B1 INDOLINE DERIVATIVES AS DDR1 AND DDR2 INHIBITORS CHIESI FARM SPA (IT) 2026-02-18 EP disclosed
EP-4313972-B1 INDOLINE DERIVATIVES AS DDRS INHIBITORS CHIESI FARM SPA (IT) 2025-01-29 EP disclosed
US-20240217967-A1 INDOLINE DERIVATIVES AS DDRS INHIBITORS CHIESI FARMACEUTICI S.P.A. (IT) 2024-07-04 US disclosed
US-20240217967-A1 INDOLINE DERIVATIVES AS DDRS INHIBITORS CHIESI FARMACEUTICI S.P.A. (IT) 2024-07-04 US disclosed
US-20240190847-A1 INDOLINE DERIVATIVES AS DDR1 AND DDR2 INHIBITORS CHIESI FARMACEUTICI S.P.A. (IT) 2024-06-13 US disclosed
EP-4313972-A1 INDOLINE DERIVATIVES AS DDRS INHIBITORS Chiesi Farmaceutici S.p.A. (IT) 2024-02-07 EP disclosed
EP-4313292-A1 INDOLINE DERIVATIVES AS DDR1 AND DDR2 INHIBITORS Chiesi Farmaceutici S.p.A. (IT) 2024-02-07 EP disclosed
CN-117120434-A Indoline derivatives as DDR1 and DDR2 inhibitors 奇斯药制品公司 2023-11-24 CN disclosed
CN-117062812-A Indoline derivatives as DDR inhibitors 奇斯药制品公司 2023-11-14 CN disclosed
WO-2022200576-A1 INDOLINE DERIVATIVES AS DDR1 AND DDR2 INHIBITORS CHIESI FARMACEUTICI S.P.A. (IT) 2022-09-29 WO disclosed
WO-2022200577-A1 INDOLINE DERIVATIVES AS DDRS INHIBITORS CHIESI FARMACEUTICI S.P.A. (IT) 2022-09-29 WO disclosed
EP-1926711-B1 NOVEL HETEROBICYCLIC DERIVATIVES USEFUL AS INHIBITORS OF LIVER CARNITINE PALMITOYL TRANSFERASE HOFFMANN LA ROCHE (CH) 2012-11-07 EP disclosed
CN-101263116-B Novel heterobicyclic derivatives useful as liver carnitine palmitoyl transferase inhibitors HOFFMAN-LA ROCHE LTD. (CH) 2011-12-07 CN disclosed
US-7713996-B2 Indolyl derivatives which are L-CPT1 inhibitors HOFFMANN-LA ROCHE INC. (US) 2010-05-11 US disclosed
CN-101263116-A Novel heterobicyclic derivatives useful as liver carnitine palmitoyl transferase inhibitors HOFFMANN LA ROCHE (CH) 2008-09-10 CN disclosed
EP-1926711-A1 NOVEL HETEROBICYCLIC DERIVATIVES USEFUL AS INHIBITORS OF LIVER CARNITINE PALMITOYL TRANSFERASE F.HOFFMANN-LA ROCHE AG (CH) 2008-06-04 EP disclosed
WO-2007031429-A1 NOVEL HETEROBICYCLIC DERIVATIVES USEFUL AS INHIBITORS OF LIVER CARNITINE PALMITOYL TRANSFERASE F. HOFFMANN-LA ROCHE AG (CH) 2007-03-22 WO disclosed
US-20070060567-A1 Novel indolyl derivatives which are L-CPT1 inhibitors F. HOFFMANN-LA ROCHE AG, A SWISS COMPANY (CH) 2007-03-15 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 (3 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-20070060567-A1 Novel indolyl derivatives which are L-CPT1 inhibitors CPT1A, CPT1B, CPT2 HDAC1 580/4885HDAC6 1522/4885XIAP 2285/4885
US-20240190847-A1 INDOLINE DERIVATIVES AS DDR1 AND DDR2 INHIBITORS DDR1, DDR2, DDRGK1 HDAC1 1463/4885HDAC6 1532/4885XIAP 1804/4885
US-20240217967-A1 INDOLINE DERIVATIVES AS DDRS INHIBITORS DDR1, DDR2, DDRGK1 HDAC1 1625/4885HDAC6 1289/4885XIAP 1730/4885

“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.