SCHEMBL485160

SCHEMBL485160

CC(C)(C)OC(=O)N1CCC2(CCCNC2)CC1

nearest known ligand 0.48

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
USP2 O75604 3/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
ALDH1A1 P00352 2/20 0.44
HSD17B10 Q99714 1/20 0.42
HPGD P15428 1/20 0.41
EPHX1 P07099 1/20 0.40
ACACB O00763 2/20 0.39
GPR119 Q8TDV5 3/20 0.38
EPHX2 P34913 1/20 0.38
CYP3A4 P08684 1/20 0.38
CYP11B2 P19099 1/20 0.37

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
Hydrochloric Acid SCHEMBL15378006 0.99 USP2 (0.43) USP2SMN1; SMN2ALDH1A1HSD17B10HPGD
SCHEMBL484745 0.92 ALDH1A1 (0.50) USP2SMN1; SMN2ALDH1A1HSD17B10ACACB
SCHEMBL484585 0.91 USP2 (0.46) USP2SMN1; SMN2HPGDACACBGPR119
Hydrochloric Acid SCHEMBL5322449 0.90 ALDH1A1 (0.49) USP2SMN1; SMN2ALDH1A1HSD17B10ACACB
Hydrochloric Acid SCHEMBL896891 0.90 USP2 (0.45) USP2SMN1; SMN2HPGDACACBGPR119
Oxalic Acid SCHEMBL29782913 0.88 HSD17B10 (0.49) USP2ALDH1A1HSD17B10ACACBCYP3A4
SCHEMBL21801899 0.87 HPGD (0.46) USP2SMN1; SMN2ALDH1A1HPGDEPHX1
SCHEMBL14801521 0.87 ALDH1A1 (0.42) USP2SMN1; SMN2ALDH1A1HSD17B10HPGD
SCHEMBL994268 0.86 USP2 (0.50) USP2SMN1; SMN2HPGDEPHX1ACACB
SCHEMBL484938 0.86 ALDH1A1 (0.45) USP2SMN1; SMN2ALDH1A1HSD17B10HPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2569304-A1 SUBSTITUTED N-HETEROARYL SPIROLACTAM BIPYRROLIDINES, PREPARATION AND THERAPEUTIC USE THEREOF SANOFI (FR) 2013-03-20 EP claimed
WO-2011143148-A1 SUBSTITUTED N-HETEROARYL SPIROLACTAM BIPYRROLIDINES, PREPARATION AND THERAPEUTIC USE THEREOF SANOFI (FR) 2011-11-17 WO claimed
US-12448389-B2 BRM targeting compounds and associated methods of use PRELUDE THERAPEUTICS INCORPORATED (US) 2025-10-21 US disclosed
US-20250136611-A1 HETEROBIFUNCTIONAL COMPOUNDS AND METHODS OF TREATING DISEASE HALDA THERAPEUTICS OPCO, INC. 2025-05-01 US disclosed
WO-2025085738-A1 HETEROBIFUNCTIONAL COMPOUNDS AND METHODS OF TREATING DISEASE HALDA THERAPEUTICS OPCO, INC. (US) 2025-04-24 WO disclosed
CN-119301132-A Halogenated indole macrocyclic compounds for the treatment of cancer 豪夫迈·罗氏有限公司 2025-01-10 CN disclosed
CN-118027003-B PROTAC compound, preparation method thereof and application of PROTAC compound as estrogen receptor degradation agent 山东大学 2024-10-29 CN disclosed
CN-118812521-A Benzo heterocyclic compound and application thereof 中科中山药物创新研究院 2024-10-22 CN disclosed
US-20240269298-A1 PHOSPHONYL DERIVATIVE, AND COMPOSITION AND PHARMACEUTICAL APPLICATION THEREOF XIZANG HAISCO PHARMACEUTICAL CO., LTD. (CN) 2024-08-15 US disclosed
US-20240270739-A1 Heteroaryl Fluoroalkenes As DGK Inhibitors INCYTE CORPORATION 2024-08-15 US disclosed
US-20240254115-A1 New Pyridine-Sulfonamide Derivatives as Sigma Ligands ACONDICIONAMIENTO TARRASENSE (ES) 2024-08-01 US disclosed
WO-2011034907-A2 PROTEIN KINASE CONJUGATES AND INHIBITORS AVILA THERAPEUTICS, INC. (US) 2011-03-24 WO disclosed
WO-2011034741-A1 IMIDAZOPYRIDIN-2-ONE DERIVATIVES MERCK SHARP & DOHME CORP. (US) 2011-03-24 WO disclosed
US-20100249095-A1 Substituted Spiro-amide Compounds GRUENENTHAL GMBH (DE) 2010-09-30 US disclosed
WO-2010108651-A1 SUBSTITUTED SPIRO-AMIDE COMPOUNDS Grünenthal GmbH (DE) 2010-09-30 WO disclosed
EP-2215085-A2 PYRIDINE AND PYRAZINE DERIVATIVES USEFUL IN THE TREATMENT OF CELL PROLIFERATIVE DISORDERS AstraZeneca AB (SE) 2010-08-11 EP disclosed
US-20090118305-A1 PYRIDINE AND PYRAZINE DERIVATIVES - 083 ASTRAZENECA AB (SE) 2009-05-07 US disclosed
WO-2009053737-A2 PYRIDINE AND PYRAZINE DERIVATIVES USEFUL IN THE TREATMENT OF CELL PROLIFERATIVE DISORDERS ASTRAZENECA AB (SE) 2009-04-30 WO disclosed
US-20080247964-A1 SUBSTITUTED AZASPIRO DERIVATIVES NEUROGEN CORPORATION 2008-10-09 US disclosed
US-20080247964-A1 SUBSTITUTED AZASPIRO DERIVATIVES NEUROGEN CORPORATION 2008-10-09 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-20240269298-A1 PHOSPHONYL DERIVATIVE, AND COMPOSITION AND PHARMACEUTICAL APPLICATION THEREOF EGFR, BLK, CSNK1A1L USP2 4695/4885SMN1; SMN2 4694/4885ALDH1A1 4631/4885
US-20250136611-A1 HETEROBIFUNCTIONAL COMPOUNDS AND METHODS OF TREATING DISEASE VHL, BRCA1, TP53 USP2 3195/4885SMN1; SMN2 1670/4885ALDH1A1 246/4885
US-20240254115-A1 New Pyridine-Sulfonamide Derivatives as Sigma Ligands SIGMAR1, TMEM97, OPRD1 USP2 2065/4885SMN1; SMN2 3118/4885ALDH1A1 1011/4885
US-20080247964-A1 SUBSTITUTED AZASPIRO DERIVATIVES HRH3, HRH4, HRH1 USP2 3600/4885SMN1; SMN2 838/4885ALDH1A1 734/4885
US-20100249095-A1 Substituted Spiro-amide Compounds BDKRB1, BDKRB2, REN USP2 4864/4885SMN1; SMN2 3545/4885ALDH1A1 2086/4885
US-20240270739-A1 Heteroaryl Fluoroalkenes As DGK Inhibitors DGKA, DGKG, DGKK USP2 2393/4885SMN1; SMN2 4771/4885ALDH1A1 2923/4885
US-12448389-B2 BRM targeting compounds and associated methods of use ADRM1, BRDT, RBX1 USP2 55/4885SMN1; SMN2 2559/4885ALDH1A1 4038/4885
US-20090118305-A1 PYRIDINE AND PYRAZINE DERIVATIVES - 083 MKI67, CCND3, CCND1 USP2 4497/4885SMN1; SMN2 2234/4885ALDH1A1 802/4885

“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.