SCHEMBL10189678

SCHEMBL10189678

COC(=O)C1CCc2nccc(=O)n21

nearest known ligand 0.41

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
ADRB3 P13945 1/20 0.41
KMT2A Q03164 3/20 0.39
KDM4E B2RXH2 1/20 0.35
SMN1; SMN2 Q16637 2/20 0.34
MEN1 O00255 2/20 0.34
FKBP1A P62942 1/20 0.34
MMP2 P08253 4/20 0.33
ANPEP P15144 4/20 0.33
F2 P00734 1/20 0.33
F7 P08709 1/20 0.33
F3 P13726 1/20 0.33
OPRM1 P35372 2/20 0.33
OPRD1 P41143 2/20 0.33
OPRK1 P41145 2/20 0.33
OGFRL1 Q5TC84 2/20 0.33
PORCN Q9H237 1/20 0.33
ALDH1A1 P00352 1/20 0.32

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
SCHEMBL11964111 1.00 ADRB3 (0.41) ADRB3KMT2AKDM4ESMN1; SMN2MEN1
SCHEMBL11964114 0.82 ADRB3 (0.44) ADRB3KMT2AKDM4ESMN1; SMN2MEN1
SCHEMBL10189486 0.82 ADRB3 (0.44) ADRB3KMT2AKDM4ESMN1; SMN2MEN1
SCHEMBL29143357 0.82 ADRB3 (0.42) ADRB3SMN1; SMN2F2F7F3
SCHEMBL29143356 0.82 ADRB3 (0.42) ADRB3SMN1; SMN2F2F7F3
SCHEMBL30148124 0.81 ADRB3 (0.41) ADRB3KMT2AKDM4EMEN1F2
SCHEMBL31264968 0.81 ADRB3 (0.43) ADRB3KMT2AKDM4ESMN1; SMN2MEN1
SCHEMBL16188164 0.80 ADRB3 (0.41) ADRB3SMN1; SMN2F2F7F3
SCHEMBL31119161 0.79 ADRB3 (0.40) ADRB3
SCHEMBL30715263 0.76 LMNA (0.41) KMT2ASMN1; SMN2MEN1OPRM1OPRD1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117756809-A Synthesis method of (6S) 4,6,7, 8-tetrahydro-4-oxo pyrrolo [1,2-A ] pyrimidine-6-carboxylic acid methyl ester 苏州莱克施德药业有限公司 2024-03-26 CN claimed
CN-117756809-A Synthesis method of (6S) 4,6,7, 8-tetrahydro-4-oxo pyrrolo [1,2-A ] pyrimidine-6-carboxylic acid methyl ester 苏州莱克施德药业有限公司 2024-03-26 CN disclosed
CN-117756809-A Synthesis method of (6S) 4,6,7, 8-tetrahydro-4-oxo pyrrolo [1,2-A ] pyrimidine-6-carboxylic acid methyl ester 苏州莱克施德药业有限公司 2024-03-26 CN disclosed
CN-117756809-A Synthesis method of (6S) 4,6,7, 8-tetrahydro-4-oxo pyrrolo [1,2-A ] pyrimidine-6-carboxylic acid methyl ester 苏州莱克施德药业有限公司 2024-03-26 CN disclosed
US-11091493-B2 Process for preparing beta 3 agonists and intermediates MERCK SHARP & DOHME CORP. (US) 2021-08-17 US disclosed
US-20200392141-A1 PROCESS FOR PREPARING BETA 3 AGONISTS AND INTERMEDIATES MERCK SHARP & DOHME CORP. 2020-12-17 US disclosed
EP-2968269-B1 PROCESS FOR PREPARING BETA 3 AGONISTS AND INTERMEDIATES MERCK SHARP & DOHME (US) 2019-07-10 EP disclosed
US-10287289-B2 Process for preparing beta 3 agonists and intermediates MERCK SHARP & DOHME CORP. (US) 2019-05-14 US disclosed
US-20170145014-A1 PROCESS FOR PREPARING BETA 3 AGONISTS AND INTERMEDIATES MERCK SHARP & DOHME CORP. (US) 2017-05-25 US disclosed
US-20120258963-A1 HYDROXYMETHYL PYRROLIDINES AS BETA 3 ADRENERGIC RECEPTOR AGONISTS MERCK SHARP & DOHME CORP. 2012-10-11 US disclosed
US-20120202819-A1 COMBINATION THERAPY USING A BETA 3 ADRENERGIC RECEPTOR AGONISTS AND AN ANTIMUSCARINIC AGENT MERCK SHARP & DOHME CORPORATION (US) 2012-08-09 US disclosed
WO-2012012314-A1 NOVEL PYRROLIDINE DERIVED BETA 3 ADRENERGIC RECEPTOR AGONISTS MERCK SHARP & DOHME CORP. (US) 2012-01-26 WO disclosed
WO-2011043942-A1 COMBINATION THERAPY USING A BETA 3 ADRENERGIC RECEPTOR AGONIST AND AN ANTIMUSCARINIC AGENT MERCK SHARP & DOHME CORP. (US) 2011-04-14 WO disclosed
US-20110028481-A1 HYDROXYMETHYL PYRROLIDINES AS BETA 3 ADRENERGIC RECEPTOR AGONISTS MERCK SHARP & DOHME CORP. 2011-02-03 US disclosed
WO-2009124166-A1 HYDROXYMETHYL PYRROLIDINES AS BETA 3 ADRENERGIC RECEPTOR AGONISTS MERCK & CO., INC. (US) 2009-10-08 WO disclosed
US-20090253705-A1 HYDROXYMETHYL PYRROLIDINES AS BETA 3 ADRENERGIC RECEPTOR AGONISTS MERCK SHARP & DOHME LLC 2009-10-08 US disclosed
WO-2009124167-A1 HYDROXYMETHYL PYRROLIDINES AS BETA 3 ADRENERGIC RECEPTOR AGONISTS MERCK & CO., INC. (US) 2009-10-08 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 (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-20110028481-A1 HYDROXYMETHYL PYRROLIDINES AS BETA 3 ADRENERGIC RECEPTOR AGONISTS ADRB3, ADRB1, ADRB2 ADRB3 1/4885KMT2A 2315/4885KDM4E 1791/4885
US-20120258963-A1 HYDROXYMETHYL PYRROLIDINES AS BETA 3 ADRENERGIC RECEPTOR AGONISTS ADRB3, ADRB1, ADRB2 ADRB3 1/4885KMT2A 2315/4885KDM4E 1791/4885
US-20090253705-A1 HYDROXYMETHYL PYRROLIDINES AS BETA 3 ADRENERGIC RECEPTOR AGONISTS ADRB3, ADRB1, ADRB2 ADRB3 1/4885KMT2A 2315/4885KDM4E 1791/4885
US-11091493-B2 Process for preparing beta 3 agonists and intermediates ADRB3, ADRA1D, ADRB1 ADRB3 1/4885KMT2A 3639/4885KDM4E 2348/4885
US-20200392141-A1 PROCESS FOR PREPARING BETA 3 AGONISTS AND INTERMEDIATES ADRB3, ADRA1D, ADRB1 ADRB3 1/4885KMT2A 3769/4885KDM4E 2488/4885
US-20120202819-A1 COMBINATION THERAPY USING A BETA 3 ADRENERGIC RECEPTOR AGONISTS AND AN ANTIMUSCARINIC AGENT ADRB2, ADRB3, ADRA2A ADRB3 2/4885KMT2A 2088/4885KDM4E 4364/4885
US-10287289-B2 Process for preparing beta 3 agonists and intermediates ADRB3, ADRA1D, ADRB1 ADRB3 1/4885KMT2A 3769/4885KDM4E 2488/4885
US-20170145014-A1 PROCESS FOR PREPARING BETA 3 AGONISTS AND INTERMEDIATES ADRB3, ADRA1D, ADRB1 ADRB3 1/4885KMT2A 3449/4885KDM4E 2273/4885

“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.