SCHEMBL3494048

SCHEMBL3494048

CCC(C(=O)O)C(=O)c1ccccn1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GSK3B P49841 1/20 0.56
LMNA P02545 4/20 0.53
L3MBTL1 Q9Y468 3/20 0.53
NAPRT Q6XQN6 1/20 0.53
P4HTM Q9NXG6 1/20 0.53
ALDH1A1 P00352 3/20 0.52
CES2 O00748 1/20 0.50
CES1 P23141 1/20 0.50
KMT2A Q03164 2/20 0.49
EPHX2 P34913 1/20 0.44
KDM4E B2RXH2 5/20 0.44
HTT P42858 3/20 0.44
PTPRA P18433 1/20 0.44
NPC1 O15118 3/20 0.43
PKM P14618 3/20 0.43
RAB9A P51151 3/20 0.43
SMN1; SMN2 Q16637 2/20 0.43
MITF O75030 1/20 0.43
CYP1A2 P05177 1/20 0.43
CTNNB1 P35222 1/20 0.43

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
SCHEMBL17433591 0.85 GSK3B (0.51) GSK3BLMNAL3MBTL1NAPRTP4HTM
SCHEMBL27580793 0.83 GSK3B (0.49) GSK3BLMNAL3MBTL1NAPRTP4HTM
SCHEMBL19333994 0.82 GSK3B (0.59) GSK3BLMNAL3MBTL1NAPRTP4HTM
SCHEMBL11620332 0.81 ALDH1A1 (0.50) GSK3BLMNAL3MBTL1NAPRTP4HTM
SCHEMBL27983113 0.81 CES2 (0.53) GSK3BLMNAL3MBTL1NAPRTP4HTM
SCHEMBL27983115 0.81 CES2 (0.53) GSK3BLMNAL3MBTL1NAPRTP4HTM
SCHEMBL7277861 0.81 GSK3B (0.58) GSK3BLMNAL3MBTL1NAPRTP4HTM
SCHEMBL19578168 0.81 GSK3B (0.58) GSK3BLMNAL3MBTL1NAPRTP4HTM
SCHEMBL6197746 0.81 GSK3B (0.62) GSK3BLMNAL3MBTL1NAPRTP4HTM
SCHEMBL5158739 0.80 GSK3B (0.43) GSK3BLMNAL3MBTL1NAPRTP4HTM

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
EP-1405917-B1 Process for the production of 3-Heteroaryl-3-hydroxy-propionic acid derivatives by enantioselective microbial reduction SALTIGO GMBH (DE) 2013-08-14 EP claimed
EP-1405917-A2 Process for the production of 3-Heteroaryl-3-hydroxy-propionic acid derivatives by enantioselective microbial reduction Bayer Chemicals AG (DE) 2004-04-07 EP claimed
CN-107431096-B Rectifier element, method for manufacturing the same, and wireless communication device 东丽株式会社 2021-01-15 CN disclosed
US-10490748-B2 Rectifying element, method for producing same, and wireless communication device TORAY INDUSTRIES, INC. (JP) 2019-11-26 US disclosed
CN-105190901-B Field effect transistor 东丽株式会社 2018-12-04 CN disclosed
US-20180026197-A1 RECTIFYING ELEMENT, METHOD FOR PRODUCING SAME, AND WIRELESS COMMUNICATION DEVICE TORAY INDUSTRIES, INC. (JP) 2018-01-25 US disclosed
CN-107431096-A Rectifier cell, its manufacture method and radio communication device 东丽株式会社 2017-12-01 CN disclosed
US-20160035457-A1 FIELD EFFECT TRANSISTOR TORAY INDUSTRIES, INC. (JP) 2016-02-04 US disclosed
EP-2975649-A1 FIELD EFFECT TRANSISTOR Toray Industries, Inc. (JP) 2016-01-20 EP disclosed
CN-105190901-A Field effect transistor TORAY INDUSTRIES 2015-12-23 CN disclosed
CN-103957908-A Substituted aminothiazoles as inhibitors of cancer including hepatocellular carcinoma and as inhibitors of hepatitis virus replication INST HEPATITIS & VIRUS RES 2014-07-30 CN disclosed
EP-1405917-B1 Process for the production of 3-Heteroaryl-3-hydroxy-propionic acid derivatives by enantioselective microbial reduction SALTIGO GMBH (DE) 2013-08-14 EP disclosed
US-20100121048-A1 Cyclic Amine Compound and Use Thereof for the Prophylaxis or Treatment of Hypertension TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2010-05-13 US disclosed
EP-1340746-B1 Process for the reduction of 3-heteroaryl-3-oxo-propanoic acid derivatives SALTIGO GMBH (DE) 2007-02-28 EP disclosed
EP-1405917-A2 Process for the production of 3-Heteroaryl-3-hydroxy-propionic acid derivatives by enantioselective microbial reduction Bayer Chemicals AG (DE) 2004-04-07 EP disclosed
EP-1340746-A1 Process for the reduction of 3-heteroaryl-3-oxo-propanoic acid derivatives BAYER AG (DE) 2003-09-03 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 (1 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-20100121048-A1 Cyclic Amine Compound and Use Thereof for the Prophylaxis or Treatment of Hypertension REN, AGTR1, AGTR2 GSK3B 4123/4885LMNA 201/4885L3MBTL1 3870/4885

“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.