SCHEMBL424037

SCHEMBL424037

OC[C@H](NCc1ccccc1)c1ccccc1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 1/20 0.61
ADRB2 P07550 1/20 0.55
ACP3 P15309 3/20 0.51
L3MBTL1 Q9Y468 2/20 0.49
ATM Q13315 1/20 0.49
MAN2A1 Q16706 3/20 0.47
MAN1B1 Q9UKM7 3/20 0.47
EPHX2 P34913 2/20 0.46
MAPT P10636 2/20 0.46
SIGMAR1 Q99720 1/20 0.46
MAN2B1 O00754 2/20 0.45
ALOX12 P18054 2/20 0.45
ALDH1A1 P00352 1/20 0.45
HPGD P15428 1/20 0.45
THRB P10828 1/20 0.45
IDO1 P14902 1/20 0.45
MEN1 O00255 1/20 0.44
POLB P06746 1/20 0.44
GAA P10253 1/20 0.44
KMT2A Q03164 1/20 0.44

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
SCHEMBL1848481 1.00 SMN1; SMN2 (0.61) SMN1; SMN2ADRB2ACP3L3MBTL1ATM
SCHEMBL4853220 1.00 SMN1; SMN2 (0.61) SMN1; SMN2ADRB2ACP3L3MBTL1ATM
SCHEMBL6472595 0.89 ADRB2 (0.50) SMN1; SMN2ADRB2ACP3L3MBTL1ATM
SCHEMBL6514671 0.88 ATM (0.66) SMN1; SMN2ADRB2ACP3L3MBTL1ATM
Hydrochloric Acid SCHEMBL6473470 0.88 ADRB2 (0.52) SMN1; SMN2ADRB2ACP3L3MBTL1ATM
SCHEMBL323957 0.88 ADRB2 (0.56) SMN1; SMN2ADRB2ACP3L3MBTL1ATM
SCHEMBL2602792 0.85 SMN1; SMN2 (0.57) SMN1; SMN2ADRB2ACP3L3MBTL1ATM
SCHEMBL22445577 0.84 TDP1 (0.58) ADRB2L3MBTL1ALDH1A1MEN1KMT2A
SCHEMBL12493466 0.84 TDP1 (0.58) ADRB2L3MBTL1ALDH1A1MEN1KMT2A
SCHEMBL323594 0.82 BCHE (0.55) ATMEPHX2MAPTMEN1POLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260007672-A1 INHIBITORS OF MPTP NRG THERAPEUTICS LTD (GB) 2026-01-08 US disclosed
US-12491185-B2 Inhibitors of mPTP NRG THERAPEUTICS LTD (GB) 2025-12-09 US disclosed
EP-4652162-A1 INHIBITORS OF MPTP NRG Therapeutics LTD (GB) 2025-11-26 EP disclosed
US-20250177397-A1 INHIBITORS OF MPTP NRG THERAPEUTICS LTD (GB) 2025-06-05 US disclosed
WO-2024153946-A1 INHIBITORS OF MPTP NRG THERAPEUTICS LTD (GB) 2024-07-25 WO disclosed
US-8741934-B2 Inhibitors of ion channels PFIZER LIMITED (GB) 2014-06-03 US disclosed
US-8741934-B2 Inhibitors of ion channels PFIZER LIMITED (GB) 2014-06-03 US disclosed
US-20130072471-A1 Inhibitors of Ion Channels MARRON BRIAN EDWARD (US) 2013-03-21 US disclosed
US-20130072471-A1 Inhibitors of Ion Channels MARRON BRIAN EDWARD (US) 2013-03-21 US disclosed
US-8357711-B2 Heterocyclic sulfonamides as inhibitors of ion channels PFIZER LIMITED (GB) 2013-01-22 US disclosed
US-8163944-B2 Allylic oxidations catalyzed by dirhodium catalysts under aqueous conditions UNIVERSITY OF MARYLAND COLLEGE PARK (US) 2012-04-24 US disclosed
EP-2420487-A1 NOVEL METHOD FOR PRODUCING OPTICALLY ACTIVE PYRROLIDINE COMPOUND Astellas Pharma Inc. (JP) 2012-02-22 EP disclosed
US-20120022271-A1 NOVEL METHOD FOR PRODUCING OPTICALLY ACTIVE PYRROLIDINE COMPOUND ASTELLAS PHARMA INC. (JP) 2012-01-26 US disclosed
EP-1995241-B1 Inhibitors of ion channels ICAGEN INC (US) 2010-03-17 EP disclosed
US-20090143358-A1 INHIBITORS OF ION CHANNELS ICAGEN, INC. (US) 2009-06-04 US disclosed
US-20090143358-A1 INHIBITORS OF ION CHANNELS ICAGEN, INC. (US) 2009-06-04 US disclosed
US-20090143358-A1 INHIBITORS OF ION CHANNELS ICAGEN, INC. (US) 2009-06-04 US disclosed
US-20090093638-A1 Allylic Oxidations Catalyzed by Dirhodium Catalysts under Aqueous Conditions UNIVERSITY OF MARYLAND, COLLEGE PARK (US) 2009-04-09 US disclosed
US-20090093638-A1 Allylic Oxidations Catalyzed by Dirhodium Catalysts under Aqueous Conditions UNIVERSITY OF MARYLAND, COLLEGE PARK (US) 2009-04-09 US disclosed
EP-1995241-A1 Inhibitors of ion channels ICAgen, Incorporated (US) 2008-11-26 EP 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-12491185-B2 Inhibitors of mPTP PARK7, PINK1, SNCA SMN1; SMN2 1036/4885ADRB2 424/4885ACP3 1604/4885
US-20130072471-A1 Inhibitors of Ion Channels TRPV1, TRPV5, TRPA1 SMN1; SMN2 445/4885ADRB2 2412/4885ACP3 3118/4885
US-20120022271-A1 NOVEL METHOD FOR PRODUCING OPTICALLY ACTIVE PYRROLIDINE COMPOUND PPOX, CBR3, ALDH18A1 SMN1; SMN2 4498/4885ADRB2 2312/4885ACP3 1467/4885
US-20250177397-A1 INHIBITORS OF MPTP PARK7, PINK1, SNCA SMN1; SMN2 1036/4885ADRB2 424/4885ACP3 1604/4885
US-20090143358-A1 INHIBITORS OF ION CHANNELS TRPV1, TRPV5, TRPA1 SMN1; SMN2 445/4885ADRB2 2412/4885ACP3 3118/4885
US-20260007672-A1 INHIBITORS OF MPTP PARK7, SNCA, CYC1 SMN1; SMN2 995/4885ADRB2 54/4885ACP3 4298/4885
US-20090093638-A1 Allylic Oxidations Catalyzed by Dirhodium Catalysts under Aqueous Conditions CYP11B2, DHCR7, ZDHHC7 SMN1; SMN2 4353/4885ADRB2 1731/4885ACP3 1389/4885

“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.