SCHEMBL20875014

SCHEMBL20875014

COC(=O)c1cc(Cl)c2cc[nH]c2c1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NR4A2 P43354 3/20 0.46
NPC1 O15118 1/20 0.45
AURKA O14965 2/20 0.43
TPX2 Q9ULW0 2/20 0.43
KIF11 P52732 1/20 0.43
CREBBP Q92793 1/20 0.43
RHEB Q15382 2/20 0.41
ALDH1A1 P00352 1/20 0.41
CA12 O43570 1/20 0.41
CA1 P00915 1/20 0.41
CA2 P00918 1/20 0.41
CA7 P43166 1/20 0.41
CA9 Q16790 1/20 0.41
CA14 Q9ULX7 1/20 0.41
PARP1 P09874 1/20 0.40
BCL6 P41182 1/20 0.40
BCOR Q6W2J9 1/20 0.40
PIM1 P11309 1/20 0.40
PIM3 Q86V86 1/20 0.40
MAP2K4 P45985 1/20 0.40

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
SCHEMBL6418376 0.83 NR4A2 (0.51) NR4A2NPC1KIF11CREBBPALDH1A1
SCHEMBL3578858 0.83 NPC1 (0.46) NR4A2NPC1KIF11CREBBPALDH1A1
SCHEMBL3578888 0.83 LMNA (0.53) NR4A2NPC1KIF11CREBBPALDH1A1
SCHEMBL31396294 0.81 NPC1 (0.45) NR4A2NPC1KIF11CREBBPALDH1A1
SCHEMBL3349808 0.81 KDM4E (0.49) NR4A2NPC1KIF11CREBBPALDH1A1
SCHEMBL3350847 0.81 NPC1 (0.45) NR4A2NPC1KIF11CREBBPALDH1A1
SCHEMBL3546474 0.81 NPC1 (0.45) NR4A2NPC1KIF11CREBBPRHEB
SCHEMBL29507057 0.81 NPC1 (0.45) NR4A2NPC1KIF11CREBBPRHEB
SCHEMBL3567460 0.81 TUBB4A (0.49) NR4A2NPC1KIF11CREBBPALDH1A1
SCHEMBL3548319 0.80 AURKA (0.63) AURKATPX2RHEBALDH1A1FTO

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-4739684-A1 1,6-NAPHTHRIDINE COMPOUNDS AS SMARCA2 INHIBITORS USEFUL FOR THE TREATMENT OF SMARCA4 DEFICIENT CANCERS Janssen Pharmaceutica NV (BE) 2026-05-13 EP disclosed
US-20250236624-A1 Heterocyclic Compounds as RET Kinase Inhibitors CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2025-07-24 US disclosed
WO-2025008060-A1 1,6-NAPHTHRIDINE COMPOUNDS AS SMARCA2 INHIBITORS USEFUL FOR THE TREATMENT OF SMARCA4 DEFICIENT CANCERS JANSSEN PHARMACEUTICA NV (BE) 2025-01-09 WO disclosed
CN-115650985-B Heterocyclic compounds as RET kinase inhibitors 癌症研究科技有限公司 2024-08-02 CN disclosed
US-20230339954-A1 Heterocyclic Compounds as RET Kinase Inhibitors CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2023-10-26 US disclosed
US-20230092163-A1 COMPOUNDS AND COMPOSITIONS FOR TREATING CONDITIONS ASSOCIATED WITH STING ACTIVITY NOVARTIS PHARMA AG (CH) 2023-03-23 US disclosed
CN-115650985-A Heterocyclic compounds as RET kinase inhibitors 癌症研究科技有限公司 2023-01-31 CN disclosed
US-11548896-B2 Heterocyclic compounds as RET kinase inhibitors CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2023-01-10 US disclosed
CN-109195972-B Heterocyclic compounds as RET kinase inhibitors 癌症研究科技有限公司 2022-10-28 CN disclosed
EP-3983383-A1 COMPOUNDS AND COMPOSITIONS FOR TREATING CONDITIONS ASSOCIATED WITH STING ACTIVITY IFM Due, Inc. (US) 2022-04-20 EP disclosed
EP-3960180-A1 HETEROCYCLIC COMPOUNDS AS RET KINASE INHIBITORS Cancer Research Technology Limited (GB) 2022-03-02 EP disclosed
EP-3442980-B1 HETEROCYCLIC COMPOUNDS AS RET KINASE INHIBITORS CANCER RESEARCH TECH LTD (GB) 2021-06-09 EP disclosed
US-20210155628-A1 Heterocyclic Compounds as RET Kinase Inhibitors CANCER RESEARCH TECH LTD (GB) 2021-05-27 US disclosed
US-10954241-B2 Heterocyclic compounds as ret kinase inhibitors CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2021-03-23 US disclosed
WO-2020252240-A1 COMPOUNDS AND COMPOSITIONS FOR TREATING CONDITIONS ASSOCIATED WITH STING ACTIVITY IFM DUE, INC. (US) 2020-12-17 WO disclosed
WO-2020252240-A1 COMPOUNDS AND COMPOSITIONS FOR TREATING CONDITIONS ASSOCIATED WITH STING ACTIVITY IFM DUE, INC. (US) 2020-12-17 WO disclosed
US-20190106425-A1 HETEROCYCLIC COMPOUNDS AS RET KINASE INHIBITORS CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2019-04-11 US disclosed
US-20160122321-A1 Carboxamide Compounds and Methods for Using the Same MIDCAP FINANCIAL TRUST 2016-05-05 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 (8 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-20210155628-A1 Heterocyclic Compounds as RET Kinase Inhibitors RET, REL, BCR NR4A2 284/4885NPC1 3915/4885AURKA 1929/4885
US-20160122321-A1 Carboxamide Compounds and Methods for Using the Same PC, AK2, PRKAA2 NR4A2 1362/4885NPC1 3209/4885AURKA 1424/4885
US-20250236624-A1 Heterocyclic Compounds as RET Kinase Inhibitors RET, REL, BCR NR4A2 284/4885NPC1 3915/4885AURKA 1929/4885
US-20190106425-A1 HETEROCYCLIC COMPOUNDS AS RET KINASE INHIBITORS RET, REL, BCR NR4A2 284/4885NPC1 3915/4885AURKA 1929/4885
US-20230092163-A1 COMPOUNDS AND COMPOSITIONS FOR TREATING CONDITIONS ASSOCIATED WITH STING ACTIVITY STING1, CGAS, IRF3 NR4A2 2019/4885NPC1 830/4885AURKA 3474/4885
US-11548896-B2 Heterocyclic compounds as RET kinase inhibitors RET, REL, BCR NR4A2 284/4885NPC1 3915/4885AURKA 1929/4885
US-20230339954-A1 Heterocyclic Compounds as RET Kinase Inhibitors RET, REL, BCR NR4A2 284/4885NPC1 3915/4885AURKA 1929/4885
US-10954241-B2 Heterocyclic compounds as ret kinase inhibitors RET, REL, BCR NR4A2 284/4885NPC1 3915/4885AURKA 1929/4885

“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.