SCHEMBL21584052

SCHEMBL21584052

CC(=O)Oc1cc(Br)c2c(c1)CC2

nearest known ligand 0.40

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 3/20 0.40
LMNA P02545 3/20 0.40
MEN1 O00255 2/20 0.40
KMT2A Q03164 2/20 0.40
CYP3A4 P08684 2/20 0.40
KDM4E B2RXH2 1/20 0.40
TTR P02766 1/20 0.40
TP53 P04637 1/20 0.40
SMN1; SMN2 Q16637 1/20 0.40
PGR P06401 3/20 0.40
CYP19A1 P11511 1/20 0.37
PKM P14618 2/20 0.37
POLB P06746 1/20 0.37
ESR1 P03372 2/20 0.36
CA2 P00918 1/20 0.36
CA5A P35218 1/20 0.36
ALDH1A1 P00352 1/20 0.36
CYP4F2 P78329 1/20 0.36
CYP4A11 Q02928 1/20 0.36
BACE1 P56817 1/20 0.36

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
SCHEMBL2999085 0.90 PGR (0.47) MAPTLMNAMEN1KMT2ACYP3A4
SCHEMBL13864993 0.74 BACE1 (0.50) MAPTLMNAMEN1KMT2ACYP3A4
SCHEMBL7114628 0.74 CYP3A4 (0.47) MAPTLMNAMEN1KMT2ACYP3A4
SCHEMBL21584054 0.73 NPC1 (0.40) MAPTLMNATTRSMN1; SMN2CA5A
SCHEMBL7225909 0.72 MAPT (0.47) MAPTLMNAMEN1KMT2ACYP3A4
SCHEMBL2010436 0.70 LMNA (0.59) MAPTLMNAMEN1KMT2ACYP3A4
SCHEMBL28118605 0.69 CYP3A4 (0.47) MAPTLMNAMEN1KMT2ACYP3A4
SCHEMBL3453107 0.69 LMNA (0.50) MAPTLMNAMEN1KMT2ACYP3A4
SCHEMBL14710190 0.69 LMNA (0.46) MAPTLMNAMEN1KMT2ACYP3A4
SCHEMBL34461299 0.68 PGR (0.43) MAPTLMNAMEN1KMT2ACYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12630561-B2 Tricyclic derivatives inhibitor, preparation method, and applications thereof JIANGSU HANSOH PHARMACEUTICAL GROUP CO., LTD. (CN) 2026-05-19 US disclosed
EP-3805231-B1 INHIBITOR CONTAINING TRICYCLIC DERIVATIVE, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF JIANGSU HANSOH PHARMACEUTICAL GROUP CO LTD (CN) 2024-10-16 EP disclosed
CN-113227101-B Salt or crystal form containing tricyclic derivative and pharmaceutical composition thereof 上海翰森生物医药科技有限公司 2024-10-11 CN disclosed
CN-114835729-B Inhibitor containing tricyclic derivatives, preparation method and application thereof 江苏豪森药业集团有限公司 2024-05-31 CN disclosed
CN-112830935-B Crystal form containing tricyclic derivative free alkali and pharmaceutical composition thereof 上海翰森生物医药科技有限公司 2023-12-22 CN disclosed
US-20230014383-A1 THREE FUSED RING DERIVATIVE-CONTAINING SALT OR CRYSTAL FORM AND PHARMACEUTICAL COMPOSITION THEREOF JIANGSU HANSOH PHARMACEUTICAL GROUP CO., LTD. (CN) 2023-01-19 US disclosed
CN-114835729-A Tricyclic derivative inhibitor, preparation method and application thereof 江苏豪森药业集团有限公司 2022-08-02 CN disclosed
CN-110785423-B Tricyclic derivative inhibitor, preparation method and application thereof 江苏豪森药业集团有限公司 2022-07-26 CN disclosed
US-20210221822-A1 TRICYCLIC DERIVATIVES INHIBITOR, PREPARATION METHOD, AND APPLICATIONS THEREOF SHANGHAI HANSOH BIOMEDICAL CO., LTD. (CN) 2021-07-22 US disclosed
US-20210221822-A1 TRICYCLIC DERIVATIVES INHIBITOR, PREPARATION METHOD, AND APPLICATIONS THEREOF SHANGHAI HANSOH BIOMEDICAL CO., LTD. (CN) 2021-07-22 US disclosed
WO-2021104146-A1 THREE FUSED RING DERIVATIVE-CONTAINING SALT OR CRYSTAL FORM AND PHARMACEUTICAL COMPOSITION THEREOF 上海翰森生物医药科技有限公司 2021-06-03 WO disclosed
EP-3805231-A1 INHIBITOR CONTAINING TRICYCLIC DERIVATIVE, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF Jiangsu Hansoh Pharmaceutical Group Co., Ltd. (CN) 2021-04-14 EP disclosed
EP-3805231-A1 INHIBITOR CONTAINING TRICYCLIC DERIVATIVE, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF Jiangsu Hansoh Pharmaceutical Group Co., Ltd. (CN) 2021-04-14 EP disclosed
WO-2019228341-A1 INHIBITOR CONTAINING TRICYCLIC DERIVATIVE, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF 江苏豪森药业集团有限公司 (CN) 2019-12-05 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 (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-20210221822-A1 TRICYCLIC DERIVATIVES INHIBITOR, PREPARATION METHOD, AND APPLICATIONS THEREOF PIK3CA, PIK3CD, PIK3CB MAPT 2360/4885LMNA 1526/4885MEN1 2569/4885
US-20230014383-A1 THREE FUSED RING DERIVATIVE-CONTAINING SALT OR CRYSTAL FORM AND PHARMACEUTICAL COMPOSITION THEREOF AKT2, AKT3, PIK3R5 MAPT 944/4885LMNA 4011/4885MEN1 1659/4885
US-12630561-B2 Tricyclic derivatives inhibitor, preparation method, and applications thereof PIK3CA, PIK3R1, PIK3CD MAPT 4878/4885LMNA 2893/4885MEN1 3825/4885

“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.