SCHEMBL6674480

SCHEMBL6674480

CC(C)NCC(O)COc1ccc(CC(=O)O)cc1

nearest known ligand 0.78

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ADRB2 P07550 5/20 0.78
ADRB1 P08588 5/20 0.78
TDP1 Q9NUW8 3/20 0.78
LMNA P02545 2/20 0.78
PMP22 Q01453 2/20 0.78
ADRA1A P35348 2/20 0.78
CYP1A2 P05177 2/20 0.78
TSHR P16473 2/20 0.78
CNR1 P21554 1/20 0.78
ADRA1D P25100 1/20 0.78
ADRA1B P35368 1/20 0.78
KDM4E B2RXH2 1/20 0.78
GLA P06280 1/20 0.78
CYP3A4 P08684 1/20 0.78
NFKB1 P19838 1/20 0.78
THPO P40225 1/20 0.78
BLM P54132 1/20 0.78
CYP2D6 P10635 3/20 0.67
ADRB3 P13945 2/20 0.67
PTGS1 P23219 1/20 0.65

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
SCHEMBL10072155 1.00 ADRB2 (0.78) ADRB2ADRB1TDP1LMNAPMP22
SCHEMBL9628892 1.00 ADRB2 (0.78) ADRB2ADRB1TDP1LMNAPMP22
Hydrochloric Acid SCHEMBL6016823 0.99 ADRB2 (0.76) ADRB2ADRB1TDP1LMNAPMP22
SCHEMBL10961494 0.89 ADRB2 (0.78) ADRB2ADRB1TDP1LMNAPMP22
Atenolol SCHEMBL18120 0.88 ADRB2 (1.00) ADRB2ADRB1TDP1LMNAPMP22
SCHEMBL10737751 0.88 ADRB2 (0.76) ADRB2ADRB1TDP1LMNAPMP22
Atenolol SCHEMBL4362 0.88 ADRB2 (1.00) ADRB2ADRB1TDP1LMNAPMP22
SCHEMBL6016784 0.88 ADRB2 (0.77) ADRB2ADRB1TDP1LMNAPMP22
Atenolol SCHEMBL6509830 0.88 ADRB2 (1.00) ADRB2ADRB1TDP1LMNAPMP22
Esatenolol SCHEMBL4363 0.88 ADRB2 (1.00) ADRB2ADRB1TDP1LMNAPMP22

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111110854-A Composition comprising a histamine release-promoting substance and an inhibitory compound 黄泳华 2020-05-08 CN claimed
EP-0256586-B1 PROCESS FOR THE PREPARATION OF ESTERS OF 4-(2,3-EPOXYPROPOXY)PHENYLACETIC ACID AND 4-(2-HYDROXY-3-ISOPROPYLAMINO-PROPOXY)PHENYLACETIC ACID AND/OR ATENOLOL IN STEREOSPECIFIC FORM GIST-BROCADES N.V. (NL) 1992-05-13 EP claimed
CN-1031397-A The method of the stereospecific form of preparation 4-(2,3 one glycidoxy)-phenylacetate and 4-(different phenylamino one propoxy-of 2-hydroxyl-3-)-phenylacetate and/or 4-(2-hydroxyl-3-isopropylamino propoxy-)-phenylacetamide GIST BROCADES NV (NL) 1989-03-01 CN claimed
EP-0256586-A1 Process for the preparation of esters of 4-(2,3-epoxypropoxy)phenylacetic acid and 4-(2-hydroxy-3-isopropylamino-propoxy)phenylacetic acid and/or atenolol in stereospecific form GIST-BROCADES N.V. (NL) 1988-02-24 EP claimed
CN-111110854-A Composition comprising a histamine release-promoting substance and an inhibitory compound 黄泳华 2020-05-08 CN disclosed
US-7229782-B1 Antibodies specific to multiple beta blockers and methods for their use LABONE, INC. (US) 2007-06-12 US disclosed
US-7229782-B1 Antibodies specific to multiple beta blockers and methods for their use LABONE, INC. (US) 2007-06-12 US disclosed
US-6680047-B2 FOR USE IN ULTRASOUND IMAGING, CONTRAST AGENTS AMERSHAM HEALTH AS (NO) 2004-01-20 US disclosed
US-20020102217-A1 Diagnostic/therapeutic agents NYCOMED IMAGING AS 2002-08-01 US disclosed
EP-1007101-A2 IMPROVEMENTS IN OR RELATING TO DIAGNOSTIC/THERAPEUTIC AGENTS Marsden, John Christopher (GB) 2000-06-14 EP disclosed
WO-1998018500-A2 IMPROVEMENTS IN OR RELATING TO DIAGNOSTIC/THERAPEUTIC AGENTS MARSDEN, JOHN, CHRISTOPHER (GB) 1998-05-07 WO disclosed
EP-0256586-B1 PROCESS FOR THE PREPARATION OF ESTERS OF 4-(2,3-EPOXYPROPOXY)PHENYLACETIC ACID AND 4-(2-HYDROXY-3-ISOPROPYLAMINO-PROPOXY)PHENYLACETIC ACID AND/OR ATENOLOL IN STEREOSPECIFIC FORM GIST-BROCADES N.V. (NL) 1992-05-13 EP disclosed
EP-0256586-B1 PROCESS FOR THE PREPARATION OF ESTERS OF 4-(2,3-EPOXYPROPOXY)PHENYLACETIC ACID AND 4-(2-HYDROXY-3-ISOPROPYLAMINO-PROPOXY)PHENYLACETIC ACID AND/OR ATENOLOL IN STEREOSPECIFIC FORM GIST-BROCADES N.V. (NL) 1992-05-13 EP disclosed
CN-1016074-B PROCESS FOR PREPARING ESTERS OF 4-(2-HYDROXY-3-ISOPROPYLAMINO-PROPOXY) PHENYLACETIC ACID AND/OR ATENOLOL IN STEREOSPECIFIC FORM GIST BROCADES NV (NL) 1992-04-01 CN disclosed
EP-0256586-A1 Process for the preparation of esters of 4-(2,3-epoxypropoxy)phenylacetic acid and 4-(2-hydroxy-3-isopropylamino-propoxy)phenylacetic acid and/or atenolol in stereospecific form GIST-BROCADES N.V. (NL) 1988-02-24 EP disclosed
EP-0256586-A1 Process for the preparation of esters of 4-(2,3-epoxypropoxy)phenylacetic acid and 4-(2-hydroxy-3-isopropylamino-propoxy)phenylacetic acid and/or atenolol in stereospecific form GIST-BROCADES N.V. (NL) 1988-02-24 EP disclosed