SCHEMBL165789

SCHEMBL165789

C1CCN(C2CCC2)CC1

nearest known ligand 0.71

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
L3MBTL3 Q96JM7 7/20 0.48
L3MBTL1 Q9Y468 6/20 0.48
HTR6 P50406 1/20 0.48
MBTD1 Q05BQ5 4/20 0.43
CYP2D6 P10635 1/20 0.43
CYP2C19 P33261 1/20 0.43
PHGDH O43175 1/20 0.43
MGLL Q99685 1/20 0.43
SLC18A3 Q16572 1/20 0.41
MEN1 O00255 1/20 0.41
KMT2A Q03164 1/20 0.41

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
SCHEMBL17619719 1.00 L3MBTL3 (0.48) L3MBTL3L3MBTL1HTR6MBTD1CYP2D6
SCHEMBL14098366 0.97
SCHEMBL29058882 0.94 HTR6 (0.50) L3MBTL3L3MBTL1HTR6MBTD1CYP2D6
SCHEMBL60131 0.93 HTR6 (0.54) L3MBTL3L3MBTL1HTR6MBTD1CYP2D6
SCHEMBL22216666 0.93 HTR6 (0.54) L3MBTL3L3MBTL1HTR6MBTD1CYP2D6
SCHEMBL24782761 0.93 HTR6 (0.54) L3MBTL3L3MBTL1HTR6MBTD1CYP2D6
SCHEMBL21057384 0.93 HTR6 (0.54) L3MBTL3L3MBTL1HTR6MBTD1CYP2D6
SCHEMBL21057351 0.93 HTR6 (0.54) L3MBTL3L3MBTL1HTR6MBTD1CYP2D6
SCHEMBL1828721 0.93 HTR6 (0.54) L3MBTL3L3MBTL1HTR6MBTD1CYP2D6
SCHEMBL728754 0.93 HTR6 (0.54) L3MBTL3L3MBTL1HTR6MBTD1CYP2D6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025124516-A1 COMPOUND HAVING AKT KINASE-DEGRADING ACTIVITY, PREPARATION METHOD THEREFOR, AND PHARMACEUTICAL USE THEREOF 南京正大天晴制药有限公司 2025-06-19 WO claimed
CN-118525026-A Compound for inhibiting or degrading HPK1 kinase and application thereof in medicine 西藏海思科制药有限公司 2024-08-20 CN claimed
US-11787785-B2 Pyrazolopyridine derivatives and uses thereof NOVARTIS AG (CH) 2023-10-17 US claimed
WO-2023166349-A2 PHENYLUREA DERIVATIVE AND PHARMACEUTICAL USE THEREOF 杭州百诚医药科技股份有限公司 2023-09-07 WO claimed
CN-116554147-A Pyrazole derivative, composition and pharmaceutical application thereof 四川海思科制药有限公司 2023-08-08 CN claimed
WO-2023143384-A1 COMPOUND FOR INHIBITING OR DEGRADING HPK1 KINASE AND MEDICAL USE THEREOF 四川海思科制药有限公司 2023-08-03 WO claimed
CN-116375742-A Azaaromatic ring derivative, composition and pharmaceutical application thereof 海思科医药集团股份有限公司 2023-07-04 CN claimed
WO-2023109892-A1 COMPOUND FOR INHIBITING OR DEGRADING BRD9, AND COMPOSITION AND PHARMACEUTICAL USE THEREOF 海思科医药集团股份有限公司 2023-06-22 WO claimed
CN-116134028-A Compound capable of degrading BTK kinase, preparation method and pharmaceutical application thereof 四川海思科制药有限公司 2023-05-16 CN claimed
US-20230108325-A1 Pyrazolopyridine Derivatives and Uses thereof NOVARTIS AG (CH) 2023-04-06 US claimed
CN-114874286-A Compound for degrading BTK kinase, pharmaceutical composition and pharmaceutical application thereof 四川海思科制药有限公司 2022-08-09 CN claimed
CN-114805199-A Benzene ring derivative and application thereof in medicine 海思科医药集团股份有限公司 2022-07-29 CN claimed
CN-114507235-A Compound capable of degrading BTK kinase, preparation method and pharmaceutical application thereof 海思科医药集团股份有限公司 2022-05-17 CN claimed
CN-114437035-A Compound for inhibiting and degrading IRAK4, pharmaceutical composition and pharmaceutical application thereof 海思科医药集团股份有限公司 2022-05-06 CN claimed
CN-113387931-A Compound capable of inhibiting or degrading protein kinase, preparation method and pharmaceutical application thereof 四川海思科制药有限公司 2021-09-14 CN claimed
CN-113292536-A Compound capable of degrading Bcr-Abl or PARP and preparation method and pharmaceutical application thereof 四川海思科制药有限公司 2021-08-24 CN claimed
CN-112390785-A BET family bromodomain inhibitor ring derivative, preparation method and pharmaceutical application thereof 四川海思科制药有限公司 2021-02-23 CN claimed
WO-2025124516-A1 COMPOUND HAVING AKT KINASE-DEGRADING ACTIVITY, PREPARATION METHOD THEREFOR, AND PHARMACEUTICAL USE THEREOF 南京正大天晴制药有限公司 2025-06-19 WO disclosed
US-20090149438-A1 Pyrimidines as PLK inhibitors BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2009-06-11 US disclosed
WO-2009047264-A1 SPIROPYRROLIDINES AND THEIR USE AGAINST HCV AND HIV INFECTION NOVARTIS AG (CH) 2009-04-16 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-11787785-B2 Pyrazolopyridine derivatives and uses thereof HBZ, ZFX, WIZ L3MBTL3 1423/4885L3MBTL1 1501/4885HTR6 3197/4885
US-20090149438-A1 Pyrimidines as PLK inhibitors PLK2, PLK3, TYMP L3MBTL3 1217/4885L3MBTL1 849/4885HTR6 3425/4885
US-20230108325-A1 Pyrazolopyridine Derivatives and Uses thereof HBZ, ZFX, WIZ L3MBTL3 1423/4885L3MBTL1 1501/4885HTR6 3197/4885

“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.