SCHEMBL2947368

SCHEMBL2947368

C=CCOC1(CC=C)CCN(C(=O)OC(C)(C)C)CC1

nearest known ligand 0.55

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
USP2 O75604 1/20 0.41
SMN1; SMN2 Q16637 1/20 0.41
DDB1 Q16531 1/20 0.37
CRBN Q96SW2 1/20 0.37
NR1H2 P55055 1/20 0.37
HPGD P15428 1/20 0.36
GPR119 Q8TDV5 5/20 0.36
OPRD1 P41143 1/20 0.36
OPRK1 P41145 1/20 0.36
EPHX2 P34913 1/20 0.36
CTSK P43235 1/20 0.35
RECQL P46063 1/20 0.35

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
SCHEMBL16049737 0.84 USP2 (0.41) USP2SMN1; SMN2DDB1CRBNNR1H2
SCHEMBL15475694 0.83 USP2 (0.43) USP2SMN1; SMN2DDB1CRBNNR1H2
SCHEMBL26104381 0.82 USP2 (0.35) USP2SMN1; SMN2DDB1CRBNNR1H2
SCHEMBL23123884 0.81 CTSK (0.34) NR1H2CTSK
SCHEMBL31574926 0.81 USP2 (0.37) USP2SMN1; SMN2DDB1CRBNGPR119
SCHEMBL13531077 0.81 USP2 (0.43) USP2SMN1; SMN2DDB1CRBNNR1H2
SCHEMBL1224512 0.80 USP2 (0.45) USP2SMN1; SMN2DDB1CRBNNR1H2
SCHEMBL31511515 0.80 USP2 (0.45) USP2SMN1; SMN2DDB1CRBNNR1H2
SCHEMBL16433062 0.80 USP2 (0.40) USP2SMN1; SMN2DDB1CRBNNR1H2
SCHEMBL2129847 0.79 USP2 (0.44) USP2SMN1; SMN2DDB1CRBNNR1H2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11649245-B2 Cyclopropylamine compound as LSD1 inhibitor and use thereof HELIOEAST PHARMACEUTICAL CO., LTD. (CN) 2023-05-16 US disclosed
US-11649245-B2 Cyclopropylamine compound as LSD1 inhibitor and use thereof HELIOEAST PHARMACEUTICAL CO., LTD. (CN) 2023-05-16 US disclosed
WO-2022267495-A1 NITROGEN-CONTAINING OXA-SPIROCYCLIC COMPOUND AND USE THEREOF 南昌弘益药业有限公司 2022-12-29 WO disclosed
US-20220119401-A1 CYCLOPROPYLAMINE COMPOUND AS LSD1 INHIBITOR AND USE THEREOF HELIOEAST SCIENCE & TECHNOLOGY CO., LTD. (CN) 2022-04-21 US disclosed
EP-3851440-A1 CYCLOPROPYLAMINE COMPOUND AS LSD1 INHIBITOR AND USE THEREOF Medshine Discovery Inc. (CN) 2021-07-21 EP disclosed
WO-2020052649-A1 CYCLOPROPYLAMINE COMPOUND AS LSD1 INHIBITOR AND USE THEREOF 南京明德新药研发有限公司 2020-03-19 WO disclosed
US-7754886-B2 N-acylsulfonamide apoptosis promoters ABBOTT LABORATORIES (US) 2010-07-13 US disclosed
US-20090137585-A1 N-ACYLSULFONAMIDE APOPTOSIS PROMOTERS ABBOTT LABORATORIES (US) 2009-05-28 US disclosed
US-7504512-B2 N-acylsulfonamide apoptosis promoters ABBOTT LABORATORIES (US) 2009-03-17 US disclosed
EP-1286967-B1 CYCLOHEXANE DERIVATIVES AND THEIR USE AS THERAPEUTIC AGENTS MERCK SHARP & DOHME (GB) 2006-09-27 EP disclosed
US-7105507-B2 Cyclohexane derivatives and their use as therapeutic agents MERCK SHARP & DOHME LIMITED (GB) 2006-09-12 US disclosed
EP-1318978-B1 N-ACYLSULFONAMIDE APOPTOSIS PROMOTERS ABBOTT LAB (US) 2006-02-08 EP disclosed
US-20040192681-A1 N-acylsulfonamide apoptosis promoters ABBVIE INC. 2004-09-30 US disclosed
US-6720338-B2 BCL-X1 INHIBITING COMPOSITIONS AND METHODS OF PROMOTING APOPTOSIS IN A MAMMAL ABBOTT LABORATORIES 2004-04-13 US disclosed
US-20030236250-A1 Cyclohexane derivatives and their use as therapeutic agents MERCK SHARP & DOHME LTD. (GB) 2003-12-25 US disclosed
EP-1286967-A1 CYCLOHEXANE DERIVATIVES AND THEIR USE AS THERAPEUTIC AGENTS MERCK SHARP & DOHME LTD. (GB) 2003-03-05 EP disclosed
US-20020086887-A1 N-Acylsulfonamide apoptosis promoters ABBVIE INC. 2002-07-04 US disclosed
US-20020055631-A1 N-acylsulfonamide apoptosis promoters ABBOTT LABORATORIES 2002-05-09 US disclosed
WO-2001087838-A1 CYCLOHEXANE DERIVATIVES AND THEIR USE AS THERAPEUTIC AGENTS MERCK SHARP & DOHME LIMITED (GB) 2001-11-22 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 (7 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-20020086887-A1 N-Acylsulfonamide apoptosis promoters BAX, BCLAF1, BCL2 USP2 1839/4885SMN1; SMN2 1440/4885DDB1 116/4885
US-20030236250-A1 Cyclohexane derivatives and their use as therapeutic agents CNR2, CNR1, HTR1A USP2 4091/4885SMN1; SMN2 3052/4885DDB1 1737/4885
US-20020055631-A1 N-acylsulfonamide apoptosis promoters BAX, BCLAF1, BCL2 USP2 1819/4885SMN1; SMN2 1656/4885DDB1 133/4885
US-20040192681-A1 N-acylsulfonamide apoptosis promoters BAX, BCLAF1, BCL2 USP2 1839/4885SMN1; SMN2 1440/4885DDB1 116/4885
US-20220119401-A1 CYCLOPROPYLAMINE COMPOUND AS LSD1 INHIBITOR AND USE THEREOF KDM1B, KDM1A, KDM7A USP2 516/4885SMN1; SMN2 1937/4885DDB1 1865/4885
US-20090137585-A1 N-ACYLSULFONAMIDE APOPTOSIS PROMOTERS BAX, BCL2, BCOR USP2 1610/4885SMN1; SMN2 1713/4885DDB1 246/4885
US-11649245-B2 Cyclopropylamine compound as LSD1 inhibitor and use thereof KDM1B, KDM1A, KDM7A USP2 516/4885SMN1; SMN2 1937/4885DDB1 1865/4885

“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.