SCHEMBL7759502

SCHEMBL7759502

O=C(CC1CCCCC1)c1ccccn1

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HPGD P15428 2/20 0.57
RECQL P46063 1/20 0.57
ALDH1A1 P00352 2/20 0.53
KDM4E B2RXH2 1/20 0.53
HSD17B10 Q99714 1/20 0.53
SMN1; SMN2 Q16637 2/20 0.53
MEN1 O00255 2/20 0.53
KMT2A Q03164 2/20 0.53
NPC1 O15118 2/20 0.53
RAB9A P51151 2/20 0.53
PKM P14618 1/20 0.49
CYP1A2 P05177 1/20 0.49
GAA P10253 1/20 0.49
CES2 O00748 1/20 0.48
CES1 P23141 1/20 0.48
GRM5 P41594 1/20 0.48
EPHX2 P34913 2/20 0.47
LMNA P02545 1/20 0.47
NAPRT Q6XQN6 1/20 0.47
P4HTM Q9NXG6 1/20 0.47

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
SCHEMBL18230248 0.91 CES2 (0.53) HPGDRECQLALDH1A1SMN1; SMN2KMT2A
SCHEMBL18230433 0.84 MAOB (0.51) HPGDRECQLALDH1A1KDM4EHSD17B10
SCHEMBL18230251 0.84 GRM4 (0.47) ALDH1A1CES2CES1LMNANAPRT
SCHEMBL38661644 0.81 CTNNB1 (0.44) HPGDRECQLALDH1A1SMN1; SMN2CES2
SCHEMBL9843696 0.81 HPGD (0.48) HPGDRECQLALDH1A1KDM4EHSD17B10
SCHEMBL5443678 0.78 HTR3E (0.44) ALDH1A1SMN1; SMN2KMT2ACES2CES1
SCHEMBL5443676 0.78 HTR3E (0.44) ALDH1A1SMN1; SMN2KMT2ACES2CES1
SCHEMBL10571875 0.76 HPGD (0.64) HPGDRECQLALDH1A1KDM4EHSD17B10
SCHEMBL31098460 0.76 SMN1; SMN2 (0.47) HPGDRECQLALDH1A1KDM4EHSD17B10
SCHEMBL18236306 0.76 L3MBTL1 (0.46) ALDH1A1KDM4EHSD17B10SMN1; SMN2GAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2026101698-A1 HEPCIDIN MIMETIC COMPOUNDS AND USES THEREOF PROTAGONIST THERAPEUTICS, INC. (US) 2026-05-15 WO disclosed
US-10087173-B2 Substituted aminothiazoles as inhibitors of cancers, including hepatocellular carcinoma, and as inhibitors of hepatitis virus replication BARUCH S. BLUMBERG INSTITUTE 2018-10-02 US disclosed
US-20170066758-A1 SUBSTITUTED AMINOTHIAZOLES AS INHIBITORS OF CANCERS, INCLUDING HEPATOCELLULAR CARCINOMA, AND AS INHIBITORS OF HEPATITIS VIRUS REPLICATION INSTITUTE FOR HEPATITIS AND VIRUS RESEARCH 2017-03-09 US disclosed
US-20170066758-A1 SUBSTITUTED AMINOTHIAZOLES AS INHIBITORS OF CANCERS, INCLUDING HEPATOCELLULAR CARCINOMA, AND AS INHIBITORS OF HEPATITIS VIRUS REPLICATION INSTITUTE FOR HEPATITIS AND VIRUS RESEARCH 2017-03-09 US disclosed
US-20170066758-A1 SUBSTITUTED AMINOTHIAZOLES AS INHIBITORS OF CANCERS, INCLUDING HEPATOCELLULAR CARCINOMA, AND AS INHIBITORS OF HEPATITIS VIRUS REPLICATION INSTITUTE FOR HEPATITIS AND VIRUS RESEARCH 2017-03-09 US disclosed
US-20140249154-A1 SUBSTITUTED AMINOTHIAZOLES AS INHIBITORS OF CANCERS, INCLUDING HEPATOCELLULAR CARCINOMA, AND AS INHIBITORS OF HEPATITIS VIRUS REPLICATION BARUCH S. BLUMBERG INSTITUTE 2014-09-04 US disclosed
US-20140249154-A1 SUBSTITUTED AMINOTHIAZOLES AS INHIBITORS OF CANCERS, INCLUDING HEPATOCELLULAR CARCINOMA, AND AS INHIBITORS OF HEPATITIS VIRUS REPLICATION BARUCH S. BLUMBERG INSTITUTE 2014-09-04 US disclosed
US-20140249154-A1 SUBSTITUTED AMINOTHIAZOLES AS INHIBITORS OF CANCERS, INCLUDING HEPATOCELLULAR CARCINOMA, AND AS INHIBITORS OF HEPATITIS VIRUS REPLICATION BARUCH S. BLUMBERG INSTITUTE 2014-09-04 US disclosed
EP-0697404-B1 New enantiomerically pure pyridyl cycloalkylethyl amines and their salts as well as process for their production BOEHRINGER INGELHEIM PHARMA (DE) 2001-04-18 EP disclosed
US-5767279-A Enantiomerically pure pyridylcycloalkylethylamines and the salts thereof and processes for preparing them BOEHRINGER INGELHEIM GMBH (DE) 1998-06-16 US disclosed
EP-0697404-A1 New enantiomerically pure pyridyl cycloalkylethyl amines and their salts as well as process for their production BOEHRINGER INGELHEIM KG (DE) 1996-02-21 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 (3 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-10087173-B2 Substituted aminothiazoles as inhibitors of cancers, including hepatocellular carcinoma, and as inhibitors of hepatitis virus replication HDGF, HCCS, BCAT1 HPGD 2172/4885RECQL 2346/4885ALDH1A1 951/4885
US-20140249154-A1 SUBSTITUTED AMINOTHIAZOLES AS INHIBITORS OF CANCERS, INCLUDING HEPATOCELLULAR CARCINOMA, AND AS INHIBITORS OF HEPATITIS VIRUS REPLICATION HCCS, BCAT1, AADAT HPGD 1961/4885RECQL 1484/4885ALDH1A1 1067/4885
US-20170066758-A1 SUBSTITUTED AMINOTHIAZOLES AS INHIBITORS OF CANCERS, INCLUDING HEPATOCELLULAR CARCINOMA, AND AS INHIBITORS OF HEPATITIS VIRUS REPLICATION HDGF, HCCS, BCAT1 HPGD 2172/4885RECQL 2346/4885ALDH1A1 951/4885

“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.