SCHEMBL5871962

SCHEMBL5871962

[CH2]c1ccc(S(=O)(=O)Cc2c(Cl)cccc2Cl)cc1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
AKR1B1 P15121 3/20 0.45
KMT2A Q03164 1/20 0.40
KDM4E B2RXH2 1/20 0.38
S1PR5 Q9H228 2/20 0.37
RXFP1 Q9HBX9 1/20 0.36
MET P08581 1/20 0.36
ADRA2B P18089 1/20 0.36
SMN1; SMN2 Q16637 2/20 0.35
NPC1 O15118 1/20 0.35
MAPT P10636 1/20 0.35
RAB9A P51151 1/20 0.35
CSNK1E P49674 1/20 0.35
CLK1 P49759 1/20 0.35
DYRK1A Q13627 1/20 0.35
DYRK2 Q92630 1/20 0.35
DYRK1B Q9Y463 1/20 0.35
GRM4 Q14833 1/20 0.35
PSEN1 P49768 1/20 0.35
PSEN2 P49810 1/20 0.35
APH1B Q8WW43 1/20 0.35

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
SCHEMBL8693173 0.83 AKR1B1 (0.49) AKR1B1KMT2ASMN1; SMN2NPC1MAPT
SCHEMBL14601731 0.82 ALDH1A1 (0.48) AKR1B1KMT2ASMN1; SMN2MAPT
SCHEMBL5598431 0.79 AKR1B1 (0.43) AKR1B1KMT2AKDM4ES1PR5RXFP1
SCHEMBL7638364 0.79 AKR1B1 (0.45) AKR1B1KMT2AKDM4ES1PR5RXFP1
SCHEMBL14458213 0.75 ALDH1A1 (0.44) AKR1B1KMT2ASMN1; SMN2MAPT
SCHEMBL14601735 0.75 KDM4E (0.55) AKR1B1KDM4ERXFP1MAPTPSEN1
SCHEMBL1272047 0.72 AKR1B1 (0.45) AKR1B1KMT2AKDM4EADRA2BSMN1; SMN2
SCHEMBL8698751 0.72 AKR1B1 (0.47) AKR1B1KMT2AKDM4EADRA2BSMN1; SMN2
SCHEMBL28336689 0.72 TSHR (0.62) SMN1; SMN2MAPT
SCHEMBL271796 0.71 AKR1B1 (0.44) AKR1B1KMT2AKDM4ERXFP1SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20060270855-A1 Methods of preparing retroviral proteases inhibitor intermediates G.D. SEARLE & CO. (US) 2006-11-30 US disclosed
US-7060851-B2 Method of preparing retroviral protease inhibitor intermediates G.D. SEARLE & CO. (US) 2006-06-13 US disclosed
US-20050131075-A1 Method of preparing retroviral protease inhibitor intermediates G.D. SEARLE & CO. (US) 2005-06-16 US disclosed
CN-1623977-A Method of preparing retroviral protease inhibitor intermediates SEARLE & CO (US) 2005-06-08 CN disclosed
US-6849760-B2 Method of preparing retroviral protease inhibitor intermediates G. D. SEARLE & CO. (US) 2005-02-01 US disclosed
US-20030171612-A1 Method of preparing retroviral protease inhibitor intermediates G.D. SEARLE & CO. 2003-09-11 US disclosed
US-6515162-B2 Precipitating or crystallizing a salt from solution; suitable as intermediates for large scale production of enzyme inhibitors, e.g. hydroxyethylamine, hydroxyethylurea and hydroxyethylsulfonamide G.D. SEARLE & CO. 2003-02-04 US disclosed
US-20010047111-A1 Method of preparing retroviral protease inhibitor intermediates NG JOHN S (US) 2001-11-29 US disclosed
EP-0804410-B1 METHOD OF PREPARING RETROVIRAL PROTEASE INHIBITOR INTERMEDIATES SEARLE & CO (US) 2001-08-29 EP disclosed
US-6201150-B1 DIASTEREOMER PURIFICATION METHOD COMPRISING PREPARING AN ORGANIC ACID OR INORGANIC ACID SALT OF AN AMINO COMPOUND AND PRECIPITATING OR CRYSTALLIZING SAID SALT FROM A SOLUTION G.D. SEARLE & CO. 2001-03-13 US disclosed
US-5831117-A ACID SALTS G. D. SEARLE & CO. (US) 1998-11-03 US disclosed
CN-1177955-A Process for preparing retroviral protease inhibitor intermediates SEARLE & CO (US) 1998-04-01 CN disclosed
EP-0804410-A1 METHOD OF PREPARING RETROVIRAL PROTEASE INHIBITOR INTERMEDIATES G.D. SEARLE & CO. (US) 1997-11-05 EP disclosed
WO-1996022275-A1 METHOD OF PREPARING RETROVIRAL PROTEASE INHIBITOR INTERMEDIATES G.D. SEARLE & CO. (US) 1996-07-25 WO 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 (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-20060270855-A1 Methods of preparing retroviral proteases inhibitor intermediates ACE, REN, MME AKR1B1 1846/4885KMT2A 1425/4885KDM4E 1543/4885
US-20030171612-A1 Method of preparing retroviral protease inhibitor intermediates ACE, REN, MME AKR1B1 1771/4885KMT2A 1342/4885KDM4E 1570/4885
US-20010047111-A1 Method of preparing retroviral protease inhibitor intermediates ACE, REN, MME AKR1B1 1771/4885KMT2A 1342/4885KDM4E 1570/4885
US-20050131075-A1 Method of preparing retroviral protease inhibitor intermediates ACE, REN, MME AKR1B1 1693/4885KMT2A 1286/4885KDM4E 1503/4885

“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.