SCHEMBL184087

SCHEMBL184087

B.c1ccc(N2CCOCC2)cc1

nearest known ligand 0.91

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.91
AKR1C3 P42330 2/20 0.60
PKM P14618 1/20 0.60
TSHR P16473 1/20 0.60
CYP2C9 P11712 1/20 0.60
CYP2C19 P33261 1/20 0.60
ALDH1A1 P00352 5/20 0.59
MAPT P10636 4/20 0.59
MEN1 O00255 2/20 0.59
HTT P42858 2/20 0.59
KMT2A Q03164 2/20 0.59
NPC1 O15118 2/20 0.59
RAB9A P51151 2/20 0.59
CYP1A2 P05177 1/20 0.59
POLB P06746 1/20 0.57
KMO O15229 1/20 0.56
AR P10275 2/20 0.55
SMN1; SMN2 Q16637 3/20 0.54
HTR3E A5X5Y0 1/20 0.54
HTR3B O95264 1/20 0.54

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
SCHEMBL254812 0.97 LMNA (0.95) LMNAAKR1C3PKMTSHRCYP2C9
SCHEMBL3948094 0.97 LMNA (0.95) LMNAAKR1C3PKMTSHRCYP2C9
SCHEMBL2555823 0.97 LMNA (0.95) LMNAAKR1C3PKMTSHRCYP2C9
SCHEMBL11203977 0.95 LMNA (1.00) LMNAAKR1C3PKMTSHRCYP2C9
Hydrochloric Acid SCHEMBL9131024 0.95 LMNA (0.91) LMNAAKR1C3PKMTSHRCYP2C9
SCHEMBL13809379 0.95 LMNA (1.00) LMNAAKR1C3PKMTSHRCYP2C9
Ammonia Solution, Strong SCHEMBL4262260 0.95 LMNA (0.91) LMNAAKR1C3PKMTSHRCYP2C9
SCHEMBL4408839 0.95 LMNA (0.91) LMNAAKR1C3PKMTSHRCYP2C9
SCHEMBL10070835 0.95 LMNA (1.00) LMNAAKR1C3PKMTSHRCYP2C9
SCHEMBL10070687 0.95 LMNA (1.00) LMNAAKR1C3PKMTSHRCYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2868659-B1 Method for producing optically active naphthalene compound MITSUBISHI TANABE PHARMA CORP (JP) 2016-05-04 EP claimed
US-9181217-B2 Method for producing optically active naphthalene compound MITSUBISHI TANABE PHARMA CORPORATION (JP) 2015-11-10 US claimed
US-20150152082-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE NAPHTHALENE COMPOUND MITSUBISHI TANABE PHARMA CORPORATION (JP) 2015-06-04 US claimed
EP-2868659-A1 Method for producing optically active naphthalene compound Mitsubishi Tanabe Pharma Corporation (JP) 2015-05-06 EP claimed
EP-2749558-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE NAPHTHALENE COMPOUND Mitsubishi Tanabe Pharma Corporation (JP) 2014-07-02 EP claimed
US-8637703-B2 Methods for synthesizing ammonia borane THE OHIO STATE UNIVERSITY (US) 2014-01-28 US claimed
US-20130237708-A1 Optically Active Cyclic Alcohol Compound And Method For Preparing The Same MITSUBISHI TANABE PHARMA CORPORATION (JP) 2013-09-12 US claimed
EP-2007743-B1 METHODS FOR SYNTHESIZING AMMONIA BORANE UNIV OHIO STATE (US) 2013-06-12 EP claimed
EP-1944291-B1 Optically active cyclic alcohol compound and method for producing same MITSUBISHI TANABE PHARMA CORP (JP) 2012-06-13 EP claimed
US-20120014857-A1 METHODS FOR SYNTHESIZING AMMONIA BORANE THE OHIO STATE UNIVERSITY (US) 2012-01-19 US claimed
US-7977508-B2 Methods for synthesizing ammonia borane THE OHIO STATE UNIVERSITY (US) 2011-07-12 US claimed
US-20100152451-A1 OPTICALLY ACTIVE CYCLIC ALCOHOL COMPOUND AND METHOD FOR PREPARING THE SAME MITSUBISHI TANABE PHARMA CORPORATION (JP) 2010-06-17 US claimed
US-20090104102-A1 METHODS FOR SYNTHESIZING AMMONIA BORANE THE OHIO STATE UNIVERSITY 2009-04-23 US claimed
EP-2007743-A2 METHODS FOR SYNTHESIZING AMMONIA BORANE The Ohio State University (US) 2008-12-31 EP claimed
EP-1944291-A1 OPTICALLY ACTIVE CYCLIC ALCOHOL COMPOUND AND METHOD FOR PRODUCING SAME Mitsubishi Tanabe Pharma Corporation (JP) 2008-07-16 EP claimed
WO-2007120511-A2 METHODS FOR SYNTHESIZING AMMONIA BORANE THE OHIO STATE UNIVERSITY (US) 2007-10-25 WO claimed
US-20050173254-A1 Nickel cobalt boron ternary alloys TASKEM, INC. 2005-08-11 US claimed
US-6875866-B2 Process for synthesis of D1 receptor antagonists SCHERING CORPORATION (US) 2005-04-05 US claimed
US-20030199690-A1 Process for synthesis of D1 receptor antagonists SCHERING CORPORATION 2003-10-23 US claimed
US-4243803-A Production of 7-(2-aminomethylphenylacetamido)-3-(1-carboxymethyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid BRISTOL-MYERS COMPANY (US) 1981-01-06 US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 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-20030199690-A1 Process for synthesis of D1 receptor antagonists OPRL1, AVPR1A, AVPR1B LMNA 3842/4885AKR1C3 432/4885PKM 1574/4885
US-20150152082-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE NAPHTHALENE COMPOUND HRH1, HRH4, RB1 LMNA 4020/4885AKR1C3 253/4885PKM 3525/4885
US-20100152451-A1 OPTICALLY ACTIVE CYCLIC ALCOHOL COMPOUND AND METHOD FOR PREPARING THE SAME ADH1C, ADH1A, ADH5 LMNA 1803/4885AKR1C3 23/4885PKM 393/4885
US-20130237708-A1 Optically Active Cyclic Alcohol Compound And Method For Preparing The Same ADH1C, ADH1A, ADH5 LMNA 1803/4885AKR1C3 23/4885PKM 393/4885

“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.