SCHEMBL154164

SCHEMBL154164

CC(C)(C)OC(=O)N1CCC(O)(CN)CC1

nearest known ligand 0.49

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
USP2 O75604 1/20 0.49
SMN1; SMN2 Q16637 1/20 0.49
HPGD P15428 1/20 0.42
EPHX2 P34913 1/20 0.41
OPRD1 P41143 1/20 0.40
OPRK1 P41145 1/20 0.40
RECQL P46063 1/20 0.40
EPHX1 P07099 1/20 0.40
DPP4 P27487 1/20 0.40
NR1H2 P55055 1/20 0.40
DDB1 Q16531 1/20 0.39
CRBN Q96SW2 1/20 0.39
ALOX15 P16050 1/20 0.38
TSHR P16473 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
Hydrochloric Acid SCHEMBL17714540 0.98 USP2 (0.47) USP2SMN1; SMN2HPGDEPHX2OPRD1
SCHEMBL22319499 0.94 HPGD (0.44) USP2SMN1; SMN2HPGDEPHX2OPRD1
SCHEMBL9773945 0.90 USP2 (0.42) USP2SMN1; SMN2HPGDEPHX2OPRD1
SCHEMBL2140971 0.87 USP2 (0.46) USP2SMN1; SMN2HPGDEPHX2OPRD1
SCHEMBL25845775 0.85 USP2 (0.47) USP2SMN1; SMN2HPGDEPHX2OPRD1
SCHEMBL18418212 0.85 USP2 (0.50) USP2SMN1; SMN2HPGDEPHX2OPRD1
SCHEMBL2349423 0.85 USP2 (0.50) USP2SMN1; SMN2HPGDEPHX2RECQL
SCHEMBL2945193 0.85 USP2 (0.50) USP2SMN1; SMN2HPGDEPHX2RECQL
SCHEMBL18669304 0.84 USP2 (0.44) USP2SMN1; SMN2HPGDEPHX2OPRD1
SCHEMBL12691337 0.84 USP2 (0.46) USP2SMN1; SMN2HPGDEPHX2OPRD1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12624053-B2 Ras inhibitors Revolution Medicines, Inc. (US) 2026-05-12 US disclosed
US-20260070930-A1 RAS INHIBITORS WILMINGTON TRUST, NATIONAL ASSOCIATION, AS ADMINISTRATIVE AGENT 2026-03-12 US disclosed
EP-4674484-A2 THIENOPYRROLE COMPOUNDS Gilead Sciences, Inc. (US) 2026-01-07 EP disclosed
US-20250388608-A1 RAS INHIBITORS WILMINGTON TRUST, NATIONAL ASSOCIATION, AS AGENT 2025-12-25 US disclosed
US-20250353854-A1 FUSED PYRIMIDINE COMPOUNDS AS INHIBITORS OF MENIN BIOMEA FUSION INC (US) 2025-11-20 US disclosed
EP-4291562-B1 THIENOPYRROLE COMPOUNDS GILEAD SCIENCES INC (US) 2025-09-10 EP disclosed
EP-4608839-A1 SPIROCYCLE CONTAINING BICYCLIC HETEROARYL COMPOUNDS Protego Biopharma, Inc. (US) 2025-09-03 EP disclosed
US-20250197423-A1 RAS INHIBITORS WILMINGTON TRUST, NATIONAL ASSOCIATION, AS AGENT 2025-06-19 US disclosed
EP-3321268-B1 BICYCLIC HETEROARYL DERIVATIVES AS MNK1 AND MNK2 MODULATORS AND USES THEREOF AGENCY SCIENCE TECH & RES (SG) 2025-06-04 EP disclosed
US-20250145643-A1 RAS INHIBITORS WILMINGTON TRUST, NATIONAL ASSOCIATION, AS AGENT 2025-05-08 US disclosed
US-20050165058-A1 Oxybenzamide derivatives useful for inhibiting factor Xa or Vlla AVENTIS PHARMA DEUTSCHLAND GMBH (DE) 2005-07-28 US disclosed
EP-1349847-B1 OXYBENZAMIDES DERIVATIVES AS FACTOR XA INHIBITORS AVENTIS PHARMA GMBH (DE) 2005-04-20 EP disclosed
WO-2005016346-A1 QUINAZOLINE ANALOGS AS RECEPTOR TYROSINE KINASE INHIBITORS ARRAY BIOPHARMA INC. (US) 2005-02-24 WO disclosed
US-20050043334-A1 Quinazoline analogs as receptor tyrosine kinase inhibitors ARRAY BIOPHARMA INC. 2005-02-24 US disclosed
CN-1481376-A HYDROXYBENZAMIDE DERIVATIVES AS FACTOR XA INHIBITORS ���ĵ�˹ҩ��¹����޹�˾ 2004-03-10 CN disclosed
EP-1349847-A1 OXYBENZAMIDES DERIVATIVES AS FACTOR XA INHIBITORS Aventis Pharma Deutschland GmbH (DE) 2003-10-08 EP disclosed
US-20030187023-A1 Sulfone derivatives, process for their production and use thereof TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2003-10-02 US disclosed
EP-1302462-A1 SULFONE DERIVATIVES, PROCESS FOR THEIR PRODUCTION AND USE THEREOF Takeda Chemical Industries, Ltd. (JP) 2003-04-16 EP disclosed
US-20020198195-A1 New oxybenzamide derivatives useful for inhibiting factor Xa or VIIa SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2002-12-26 US disclosed
WO-2002051831-A1 OXYBENZAMIDES DERIVATIVES AS FACTOR XA INHIBITORS AVENTIS PHARMA DEUTSCHLAND GMBH (DE) 2002-07-04 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 (10 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-20260070930-A1 RAS INHIBITORS KRAS, NRAS, RIN1 USP2 2484/4885SMN1; SMN2 4241/4885HPGD 1566/4885
US-20250145643-A1 RAS INHIBITORS KRAS, NRAS, HRAS USP2 1149/4885SMN1; SMN2 3728/4885HPGD 3002/4885
US-12624053-B2 Ras inhibitors KRAS, NRAS, HMGCR USP2 2102/4885SMN1; SMN2 4495/4885HPGD 1695/4885
US-20250197423-A1 RAS INHIBITORS KRAS, NRAS, HRAS USP2 1149/4885SMN1; SMN2 3728/4885HPGD 3002/4885
US-20050165058-A1 Oxybenzamide derivatives useful for inhibiting factor Xa or Vlla F12, F11, F5 USP2 1131/4885SMN1; SMN2 2054/4885HPGD 1042/4885
US-20020198195-A1 New oxybenzamide derivatives useful for inhibiting factor Xa or VIIa F9, F11, F5 USP2 2509/4885SMN1; SMN2 3360/4885HPGD 427/4885
US-20030187023-A1 Sulfone derivatives, process for their production and use thereof SULT1E1, RRS1, SHH USP2 3336/4885SMN1; SMN2 3830/4885HPGD 2397/4885
US-20250353854-A1 FUSED PYRIMIDINE COMPOUNDS AS INHIBITORS OF MENIN MEN1, MLLT1, MSI2 USP2 3835/4885SMN1; SMN2 2354/4885HPGD 2181/4885
US-20250388608-A1 RAS INHIBITORS KRAS, NRAS, HMGCR USP2 2102/4885SMN1; SMN2 4495/4885HPGD 1695/4885
US-20050043334-A1 Quinazoline analogs as receptor tyrosine kinase inhibitors ABL1, ERBB2, FLT3 USP2 3543/4885SMN1; SMN2 4722/4885HPGD 1957/4885

“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.