SCHEMBL3434993

SCHEMBL3434993

Nc1nnc(-c2ccc(Cl)cc2Cl)s1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 7/20 1.00
KDM4E B2RXH2 6/20 1.00
MGAM O43451 4/20 1.00
GAA P10253 4/20 1.00
SI P14410 4/20 1.00
MGAM2 Q2M2H8 4/20 1.00
RAB9A P51151 1/20 1.00
HPGD P15428 1/20 0.64
HSD17B10 Q99714 1/20 0.64
NOTUM Q6P988 1/20 0.58
MAPT P10636 2/20 0.53
L3MBTL1 Q9Y468 1/20 0.53
HSP90AA1 P07900 1/20 0.44
HSP90AB1 P08238 1/20 0.44
HSD11B1 P28845 1/20 0.43
MEN1 O00255 1/20 0.43
KMT2A Q03164 1/20 0.43

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
SCHEMBL11329336 0.84 ALDH1A1 (0.73) ALDH1A1KDM4EMGAMGAASI
SCHEMBL11334906 0.83 ALDH1A1 (0.71) ALDH1A1KDM4EMGAMGAASI
SCHEMBL15877021 0.83 KDM4E (0.71) ALDH1A1KDM4EMGAMGAASI
SCHEMBL12225775 0.83 KDM4E (0.71) ALDH1A1KDM4EMGAMGAASI
SCHEMBL15876804 0.83 KDM4E (0.71) ALDH1A1KDM4EMGAMGAASI
SCHEMBL11341817 0.79 ALDH1A1 (0.66) ALDH1A1KDM4EMGAMGAASI
SCHEMBL11324163 0.79 KDM4E (0.65) ALDH1A1KDM4EMGAMGAASI
SCHEMBL8045944 0.79 ALDH1A1 (0.65) ALDH1A1KDM4EMGAMGAASI
SCHEMBL29678599 0.79 ALDH1A1 (0.65) ALDH1A1KDM4EMGAMGAASI
SCHEMBL11326692 0.78 KDM4E (1.00) ALDH1A1KDM4EMGAMGAASI

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105384736-A IV type collagenase inhibitor and synthesis method thereof UNIV NANCHANG 2016-03-09 CN claimed
CN-119371374-A Green synthesis method of 2-amino-5-aryl-1, 3, 4-thiadiazole 陕西科技大学 2025-01-28 CN disclosed
EP-2594555-B1 HETEROCYCLIC COMPOUND, AND p27 KIP1 DEGRADATION INHIBITOR ASKA PHARM CO LTD (JP) 2018-03-07 EP disclosed
EP-2594555-B1 HETEROCYCLIC COMPOUND, AND p27 KIP1 DEGRADATION INHIBITOR ASKA PHARM CO LTD (JP) 2018-03-07 EP disclosed
CN-105384736-A IV type collagenase inhibitor and synthesis method thereof UNIV NANCHANG 2016-03-09 CN disclosed
US-9200008-B2 Heterocyclic compound and p27Kip1 degradation inhibitor ASKA PHARMACEUTICAL CO., LTD. (JP) 2015-12-01 US disclosed
US-9200008-B2 Heterocyclic compound and p27Kip1 degradation inhibitor ASKA PHARMACEUTICAL CO., LTD. (JP) 2015-12-01 US disclosed
US-9200008-B2 Heterocyclic compound and p27Kip1 degradation inhibitor ASKA PHARMACEUTICAL CO., LTD. (JP) 2015-12-01 US disclosed
EP-2594555-A1 HETEROCYCLIC COMPOUND, AND p27 KIP1 DEGRADATION INHIBITOR ASKA Pharmaceutical Co., Ltd. (JP) 2013-05-22 EP disclosed
EP-2594555-A1 HETEROCYCLIC COMPOUND, AND p27 KIP1 DEGRADATION INHIBITOR ASKA Pharmaceutical Co., Ltd. (JP) 2013-05-22 EP disclosed
US-20130079306-A1 HETEROCYCLIC COMPOUND AND p27Kip1 DEGRADATION INHIBITOR ASKA PHARMACEUTICAL CO., LTD. (JP) 2013-03-28 US disclosed
US-20130079306-A1 HETEROCYCLIC COMPOUND AND p27Kip1 DEGRADATION INHIBITOR ASKA PHARMACEUTICAL CO., LTD. (JP) 2013-03-28 US disclosed
US-20130079306-A1 HETEROCYCLIC COMPOUND AND p27Kip1 DEGRADATION INHIBITOR ASKA PHARMACEUTICAL CO., LTD. (JP) 2013-03-28 US disclosed
WO-2012002527-A1 HETEROCYCLIC COMPOUND, AND p27 KIP1 DEGRADATION INHIBITOR あすか製薬株式会社 (JP) 2012-01-05 WO disclosed
EP-0005783-B1 IMIDAZO (2.1-B)-(1.3.4)-THIADIAZOLES, PROCESS FOR THEIR PREPARATION AND THEIR USE IN MEDICAMENTS BAYER AG (DE) 1981-12-30 EP disclosed
US-4265898-A ANTICOAGULANTS BAYER AKTIENGESELLSCHAFT (DE) 1981-05-05 US disclosed
US-4233214-A FOR POLYACRYLONITRILE AND ACID-MODIFIED POLYESTERS OR POLYAMIDES BAYER AKTIENGESELLSCHAFT (DE) 1980-11-11 US disclosed
EP-0005783-A1 Imidazo (2.1-b)-(1.3.4)-thiadiazoles, process for their preparation and their use in medicaments BAYER AG (DE) 1979-12-12 EP disclosed
US-4036826-A Cationic azo dyestuffs with a hydroxyalkylated ammonium group BAYER AKTIENGESELLSCHAFT (DT) 1977-07-19 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-20130079306-A1 HETEROCYCLIC COMPOUND AND p27Kip1 DEGRADATION INHIBITOR CDKN1A, SKP2, CCNI ALDH1A1 1594/4885KDM4E 1069/4885MGAM 4520/4885

“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.