SCHEMBL1249700

SCHEMBL1249700

CC(=O)Nc1cc(Cl)ccc1O

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KCNMA1 Q12791 13/20 0.64
POLB P06746 2/20 0.64
KDM4E B2RXH2 3/20 0.59
HSD17B10 Q99714 1/20 0.59
LMNA P02545 2/20 0.57
SMN1; SMN2 Q16637 2/20 0.57
APOBEC3A P31941 1/20 0.57
GFER P55789 1/20 0.57
HDAC1 Q13547 1/20 0.57
APOBEC3G Q9HC16 1/20 0.57
PHPT1 Q9NRX4 1/20 0.57
MEN1 O00255 2/20 0.56
HPGD P15428 2/20 0.56
KMT2A Q03164 2/20 0.56
HIF1A Q16665 1/20 0.54
NPC1 O15118 1/20 0.54
TP53 P04637 1/20 0.54
MAPT P10636 1/20 0.54
HTT P42858 1/20 0.54
RAB9A P51151 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
SCHEMBL1952367 0.85 POLB (0.67) KCNMA1POLBKDM4EHSD17B10LMNA
SCHEMBL3782005 0.84 KDM4E (0.68) POLBKDM4EHSD17B10SMN1; SMN2HDAC1
SCHEMBL28295632 0.84 KCNMA1 (0.68) KCNMA1POLBMEN1HPGDKMT2A
SCHEMBL6814424 0.83 ALDH1A1 (0.56) KCNMA1POLBKDM4ELMNAHDAC1
SCHEMBL2388970 0.82 EPHX1 (0.70) POLBKDM4EHSD17B10LMNASMN1; SMN2
SCHEMBL9170975 0.82 POLB (0.71) KCNMA1POLBMEN1HPGDKMT2A
SCHEMBL8983170 0.82 KCNMA1 (0.57) KCNMA1POLBKDM4ELMNASMN1; SMN2
SCHEMBL7254163 0.81 KCNMA1 (0.60) KCNMA1POLBKDM4ELMNASMN1; SMN2
SCHEMBL7254652 0.81 KCNMA1 (0.61) KCNMA1POLBKDM4ELMNASMN1; SMN2
SCHEMBL9403860 0.81 KDM4E (0.59) KCNMA1POLBKDM4EHSD17B10HDAC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5149858-A Reacting with chlorine gas in presence of organic cation catalysts RHONE-POULENC CHIMIE (FR) 1992-09-22 US claimed
EP-0299891-B1 PROCESS FOR THE SELECTIVE CHLORINATION OF PHENOLIC COMPOUNDS RHONE-POULENC CHIMIE (FR) 1991-12-11 EP claimed
CN-105753730-A Method for preparing 2-amino-4-chloro-5-nitrophenol 宜兴市新宇化工有限公司 2016-07-13 CN disclosed
EP-1246792-B1 COMPOUNDS AND COMPOSITIONS FOR DELIVERING ACTIVE AGENTS EMISPHERE TECH INC (US) 2014-08-13 EP disclosed
US-20110200687-A1 BIFEPRUNOX MESYLATE MAINTENANCE DOSE COMPOSITIONS AND METHODS FOR USING THE SAME SOLVAY PHARMACEUTICALS B.V. 2011-08-18 US disclosed
US-7977506-B2 Amino acid for delivering active materials; bioavailability EMISPHERE TECHNOLOGIES, INC. (US) 2011-07-12 US disclosed
US-7964604-B2 Bifeprunox mesylate maintenance dose compositions and methods for using the same SOLVAY PHARMACEUTICALS B.V. (NL) 2011-06-21 US disclosed
EP-1656358-B1 STABLE POLYMORPH OF BIFEPRUNOX MESILATE ABBOTT HEALTHCARE PRODUCTS BV (NL) 2011-02-23 EP disclosed
EP-1891064-B1 N-AMIDE DERIVATIVES OF 8-AZABICYCLO[3.2.1]OCT-3-YL AS CCR1 ANTAGONISTS ALMIRALL SA (ES) 2009-09-02 EP disclosed
EP-1891064-B1 N-AMIDE DERIVATIVES OF 8-AZABICYCLO[3.2.1]OCT-3-YL AS CCR1 ANTAGONISTS ALMIRALL SA (ES) 2009-09-02 EP disclosed
EP-1853232-B1 STABLE CRYSTALLINE FORM OF BIFEPRUNOX MESYLATE, DOSAGE FORMS THEREOF ADN METHODS FOR USING THEM SOLVAY PHARM BV (NL) 2009-08-19 EP disclosed
WO-1998007724-A1 PROCESS FOR THE PREPARATION OF 7-ALKOXYALKYL-1,2,4-TRIAZOLO[1,5-A] PYRIMIDINE DERIVATIVES KNOLL AKTIENGESELLSCHAFT (DE) 1998-02-26 WO disclosed
US-5149858-A Reacting with chlorine gas in presence of organic cation catalysts RHONE-POULENC CHIMIE (FR) 1992-09-22 US disclosed
EP-0006220-B1 PROCESS FOR THE PREPARATION OF 3-ACYL-2-ALKYL(ARYL)-1.3.2-BENZOXAZAPHOSPHOLANES HOECHST AKTIENGESELLSCHAFT (DE) 1981-08-19 EP disclosed
EP-0006195-B1 PROCESS FOR PREPARING DELTA-3 1-OXOPHOSPHOLENES HOECHST AKTIENGESELLSCHAFT (DE) 1981-05-13 EP disclosed
US-4263231-A REACTING DICHLOROPHOSPHANES AND 2-N-ACYLAMINOPHENOLS HOECHST AKTIENGESELLSCHAFT (DE) 1981-04-21 US disclosed
US-4247488-A Process for the preparation of 1-oxophosphol-Δ3 -enes HOECHST AKTIENGESELLSCHAFT (DE) 1981-01-27 US disclosed
EP-0006195-A1 Process for preparing delta-3 1-oxophospholenes HOECHST AKTIENGESELLSCHAFT (DE) 1980-01-09 EP disclosed
EP-0006220-A1 Process for the preparation of 3-Acyl-2-alkyl(aryl)-1.3.2-benzoxazaphospholanes HOECHST AKTIENGESELLSCHAFT (DE) 1980-01-09 EP disclosed
US-4112117-A HYPOLIPIDEMIC SANDOZ, INC. (US) 1978-09-05 US 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-20110200687-A1 BIFEPRUNOX MESYLATE MAINTENANCE DOSE COMPOSITIONS AND METHODS FOR USING THE SAME LPXN, TPMT, MC2R KCNMA1 2895/4885POLB 3419/4885KDM4E 1392/4885

“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.