SCHEMBL1648260

SCHEMBL1648260

COc1c(Br)ccc(C)c1C(=O)O

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.46
HSD17B10 Q99714 2/20 0.46
KDM4E B2RXH2 1/20 0.46
PTPN1 P18031 2/20 0.42
TPMT P51580 1/20 0.42
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
MEN1 O00255 3/20 0.40
KMT2A Q03164 3/20 0.40
USP2 O75604 1/20 0.40
MAPT P10636 1/20 0.40
ALOX15 P16050 1/20 0.40
CYP2C9 P11712 2/20 0.38
LCK P06239 1/20 0.38
FYN P06241 1/20 0.38
L3MBTL1 Q9Y468 1/20 0.38

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
SCHEMBL30003496 1.00 ALDH1A1 (0.46) ALDH1A1HSD17B10KDM4EPTPN1TPMT
SCHEMBL31643643 0.84 ALDH1A1 (0.52) ALDH1A1HSD17B10KDM4EPTPN1CA12
SCHEMBL30004188 0.84 MAPT (0.43) ALDH1A1KDM4EPTPN1CA12CA1
SCHEMBL434100 0.84 MAPT (0.43) ALDH1A1KDM4EPTPN1CA12CA1
SCHEMBL24165077 0.81 HSD17B10 (0.51) ALDH1A1HSD17B10KDM4EPTPN1TPMT
SCHEMBL1323122 0.81 CA12 (0.55) ALDH1A1HSD17B10KDM4EPTPN1TPMT
SCHEMBL29693892 0.80 TDP1 (0.39) ALDH1A1HSD17B10KDM4ECA12CA1
SCHEMBL1085313 0.80 TDP1 (0.39) ALDH1A1HSD17B10KDM4ECA12CA1
SCHEMBL14720094 0.80 HSD17B10 (0.44) ALDH1A1HSD17B10KDM4EPTPN1TPMT
SCHEMBL31522091 0.80 NR1H4 (0.38) ALDH1A1MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120842067-A Synthesis method of 3-bromo-2-methoxy-6-methylbenzoic acid 青岛科技大学 2025-10-28 CN disclosed
CN-120842067-A Synthesis method of 3-bromo-2-methoxy-6-methylbenzoic acid 青岛科技大学 2025-10-28 CN disclosed
US-20250084056-A1 SUBSTITUTED OXOISOINDOLINYL PIPERIDINE-2,6-DIONE COMPOUNDS BRISTOL-MYERS SQUIBB COMPANY (US) 2025-03-13 US disclosed
WO-2025043225-A2 DEGRADERS OF CYCLIN-DEPENDENT KINASE 2 GENENTECH, INC. (US) 2025-02-27 WO disclosed
US-20240317706-A1 COMPOUNDS THAT MEDIATE PROTEIN DEGRADATION AND METHODS OF USE THEREOF MONTE ROSA THERAPEUTICS AG (CH) 2024-09-26 US disclosed
US-20240124459-A9 PRPK INHIBITORS DANA-FARBER CANCER INSTITUTE, INC. 2024-04-18 US disclosed
EP-4323350-A1 ISOINDOLINONE COMPOUNDS Monte Rosa Therapeutics AG (CH) 2024-02-21 EP disclosed
US-20240051936-A1 ISOINDOLINONE COMPOUNDS MONTE ROSA THERAPEUTICS AG (CH) 2024-02-15 US disclosed
US-20230271966-A1 PRPK INHIBITORS DANA FARBER CANCER INST INC (US) 2023-08-31 US disclosed
US-20230271966-A1 PRPK INHIBITORS DANA FARBER CANCER INST INC (US) 2023-08-31 US disclosed
CN-114450274-A Indazoles and azaindazoles as LRRK2 inhibitors 伊斯凯普生物公司 2022-05-06 CN disclosed
WO-2022005961-A1 PRPK INHIBITORS DANA-FARBER CANCER INSTITUTE, INC. (US) 2022-01-06 WO disclosed
WO-2022005961-A1 PRPK INHIBITORS DANA-FARBER CANCER INSTITUTE, INC. (US) 2022-01-06 WO disclosed
WO-2021007477-A1 INDAZOLES AND AZAINDAZOLES AS LRRK2 INHIBITORS E-SCAPE BIO, INC. (US) 2021-01-14 WO disclosed
EP-2486004-B1 SULPHONE COMPOUNDS FOR USE IN THE TREATMENT OF OBESITY ZAFGEN INC (US) 2017-05-03 EP disclosed
CN-105218329-B Intermediate of liflozin analogues and preparation method of intermediate 上海应用技术学院 2017-05-03 CN disclosed
WO-2017063327-A1 NOVEL C-SPIRO-O-GLYCOSIDE COMPOUND INTERMEDIATE AND PREPARATION METHOD THEREFOR 上海应用技术学院 2017-04-20 WO disclosed
EP-2486004-A2 SULPHONE COMPOUNDS AND METHODS OF MAKING AND USING SAME Zafgen Corporation (US) 2012-08-15 EP disclosed
WO-2011044506-A2 SULPHONE COMPOUNDS AND METHODS OF MAKING AND USING SAME ZAFGEN CORPORATION (US) 2011-04-14 WO disclosed
WO-2011044506-A2 SULPHONE COMPOUNDS AND METHODS OF MAKING AND USING SAME ZAFGEN CORPORATION (US) 2011-04-14 WO 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-20250084056-A1 SUBSTITUTED OXOISOINDOLINYL PIPERIDINE-2,6-DIONE COMPOUNDS CCNA1, CCNI, CCNE1 ALDH1A1 431/4885HSD17B10 3304/4885KDM4E 1389/4885
US-20230271966-A1 PRPK INHIBITORS PRP4K, PRPS1, PRPF6 ALDH1A1 1333/4885HSD17B10 1392/4885KDM4E 2930/4885
US-20240317706-A1 COMPOUNDS THAT MEDIATE PROTEIN DEGRADATION AND METHODS OF USE THEREOF CDK2, SKP2, CDK1 ALDH1A1 3818/4885HSD17B10 3090/4885KDM4E 2198/4885
US-20240051936-A1 ISOINDOLINONE COMPOUNDS CRBN, CDR2, POU2F2 ALDH1A1 1907/4885HSD17B10 2431/4885KDM4E 2644/4885
US-20240124459-A9 PRPK INHIBITORS PRP4K, PRPS1, PRPF6 ALDH1A1 1333/4885HSD17B10 1392/4885KDM4E 2930/4885

“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.