SCHEMBL670824

SCHEMBL670824

O=Cc1c[nH]c2c(Cl)cccc12

nearest known ligand 0.64

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
TRIM24 O15164 1/20 0.64
TRIM33 Q9UPN9 1/20 0.64
PIM1 P11309 6/20 0.54
PIM3 Q86V86 6/20 0.54
PIM2 Q9P1W9 2/20 0.53
TDO2 P48775 1/20 0.52
CYP2A6 P11509 1/20 0.52
IMPDH2 P12268 1/20 0.52
DYRK1A Q13627 1/20 0.50
AHR P35869 1/20 0.48
NR4A2 P43354 1/20 0.47
HTR2A P28223 1/20 0.47
KMT2A Q03164 2/20 0.46
DAO P14920 1/20 0.43
MEN1 O00255 1/20 0.42
ALDH1A1 P00352 1/20 0.42
TDP1 Q9NUW8 1/20 0.42
AR P10275 1/20 0.42
SLC6A4 P31645 1/20 0.42

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
SCHEMBL27868506 0.91 TRIM24 (0.54) TRIM24TRIM33PIM1PIM3PIM2
SCHEMBL29954763 0.82 TRIM24 (0.70) TRIM24TRIM33PIM1PIM3PIM2
SCHEMBL29955386 0.79 TRIM24 (0.66) TRIM24TRIM33PIM1PIM3PIM2
SCHEMBL27640740 0.79 TDO2 (0.50) TRIM24TRIM33PIM1PIM3TDO2
SCHEMBL16067373 0.78 PIM3 (0.77) TRIM24TRIM33PIM1PIM3PIM2
SCHEMBL17829692 0.78 CSNK2A2 (0.50) TRIM24TRIM33PIM1PIM3PIM2
SCHEMBL29954012 0.78 TRIM24 (0.64) TRIM24TRIM33PIM1PIM3PIM2
SCHEMBL29953184 0.78 PIM3 (0.77) TRIM24TRIM33PIM1PIM3PIM2
SCHEMBL672635 0.78 TRIM24 (1.00) TRIM24TRIM33PIM1PIM3PIM2
SCHEMBL1092989 0.78 TRIM24 (0.64) TRIM24TRIM33PIM1PIM3PIM2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102584670-B Indole-3-formaldehyde shrinkage phenylenediamine bis-schiff base and preparation method thereof SHANDONG INST LIGHT INDUSTRY 2014-04-02 CN claimed
CN-102584796-B Bis-Schiff bases synthesized by condensing indole-3-carboxaldehyde and pyridine diamine and preparation method thereof SHANDONG INST LIGHT INDUSTRY 2013-12-11 CN claimed
CN-102584671-B Bis-Schiff bases synthesized by condensing indole-3-carboxaldehyde and benzidine and preparation method thereof SHANDONG INST LIGHT INDUSTRY 2013-08-07 CN claimed
CN-102584796-A Bis-Schiff bases synthesized by condensing indole-3-carboxaldehyde and pyridine diamine and preparation method thereof SHANDONG INST LIGHT INDUSTRY 2012-07-18 CN claimed
CN-102584671-A Bis-Schiff bases synthesized by condensing indole-3-carboxaldehyde and benzidine and preparation method thereof SHANDONG INST LIGHT INDUSTRY 2012-07-18 CN claimed
CN-102584670-A Indole-3-formaldehyde shrinkage phenylenediamine bis-schiff base and preparation method thereof SHANDONG INST LIGHT INDUSTRY 2012-07-18 CN claimed
US-20250177538-A1 Methods for synthesizing deuterated formylindoles ARIZONA BOARD OF REGENTS ON BEHALF OF THE UNIVERSITY OF ARIZONA 2025-06-05 US disclosed
US-12012411-B2 Viral replication inhibitors KATHOLIEKE UNIVERSITEIT LEUVEN (BE) 2024-06-18 US disclosed
WO-2023250348-A2 METHODS FOR SYNTHESIZING DEUTERATED FORMYLINDOLES ARIZONA BOARD OF REGENTS ON BEHALF OF THE UNIVERSITY OF ARIZONA (US) 2023-12-28 WO disclosed
WO-2023183394-A1 ALPHA 1A-ADRENERGIC RECEPTOR AGONISTS AND METHODS OF USE CURASEN THERAPEUTICS, INC. (US) 2023-09-28 WO disclosed
US-20220340893-A1 BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES NUEVOLUTION A/S (DK) 2022-10-27 US disclosed
US-20220106321-A1 VIRAL REPLICATION INHIBITORS KATHOLIEKE UNIVERSITEIT LEUVEN (BE) 2022-04-07 US disclosed
US-11279704-B2 Viral replication inhibitors KATHOLIEKE UNIVERSITEIT LEUVEN (BE) 2022-03-22 US disclosed
EP-1560584-A4 FAB I INHIBITORS AFFINIUM PHARM INC (CA) 2005-10-12 EP disclosed
EP-1560584-A2 FAB I INHIBITORS Affinium Pharmaceuticals, Inc. (CA) 2005-08-10 EP disclosed
WO-2004082586-A2 PHAMACEUTICAL COMPOSITIONS COMPRISING INHIBITORS OF FAB I AND FURTHER ANTIBIOTICS AFFINIUM PHARMACEUTICALS, INC. (US) 2004-09-30 WO disclosed
US-20040147580-A1 Fab I inhibitors DEBIOPHARM INTERNATIONAL SA (CH) 2004-07-29 US disclosed
EP-1379239-A2 N-(2-ARYLETHYL) BENZYLAMINES AS ANTAGONISTS OF THE 5-HT6 RECEPTOR ELI LILLY AND COMPANY (US) 2004-01-14 EP disclosed
WO-2003088897-A2 FAB I INHIBITORS AFFINIUM PHARMACEUTICALS, INC. (CA) 2003-10-30 WO disclosed
WO-2002078693-A2 N-(2-ARYLETHYL)BENZYLAMINES AS ANTAGONISTS OF THE 5-HT6 RECEPTOR ELI LILLY AND COMPANY (US) 2002-10-10 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 (5 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-20250177538-A1 Methods for synthesizing deuterated formylindoles TDO2, CISD2, ALAD TRIM24 3946/4885TRIM33 2641/4885PIM1 4839/4885
US-11279704-B2 Viral replication inhibitors EIF2AK2, MAVS, ZC3HAV1 TRIM24 462/4885TRIM33 448/4885PIM1 1237/4885
US-20040147580-A1 Fab I inhibitors SERPINB1, TMBIM6, GDI1 TRIM24 3167/4885TRIM33 3809/4885PIM1 113/4885
US-20220106321-A1 VIRAL REPLICATION INHIBITORS EIF2AK2, MAVS, ZC3HAV1 TRIM24 462/4885TRIM33 448/4885PIM1 1237/4885
US-12012411-B2 Viral replication inhibitors EIF2AK2, MAVS, ZC3HAV1 TRIM24 462/4885TRIM33 448/4885PIM1 1237/4885

“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.