SCHEMBL376394

SCHEMBL376394

N#Cc1ncc(Cl)nc1Cl

nearest known ligand 0.42

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.42
KDM4E B2RXH2 2/20 0.42
POLB P06746 1/20 0.42
CSNK1A1 P48729 1/20 0.35
CLK4 Q9HAZ1 1/20 0.35
SYK P43405 1/20 0.35
GAA P10253 1/20 0.34
JAK3 P52333 2/20 0.34
BTK Q06187 1/20 0.34
SMN1; SMN2 Q16637 1/20 0.32
NPSR1 Q6W5P4 1/20 0.32
TDP1 Q9NUW8 1/20 0.32
PIK3CD O00329 1/20 0.31
CYP11B2 P19099 1/20 0.30

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
SCHEMBL29420836 1.00 ALDH1A1 (0.42) ALDH1A1KDM4EPOLBCSNK1A1CLK4
SCHEMBL25503292 0.84 KDM4E (0.41) ALDH1A1KDM4EPOLBCSNK1A1CLK4
SCHEMBL11086636 0.84 ALDH1A1 (0.44) ALDH1A1KDM4EPOLBCSNK1A1CLK4
SCHEMBL29380304 0.82 ALDH1A1 (0.38) ALDH1A1KDM4EPOLBCSNK1A1CLK4
SCHEMBL1338461 0.82 ALDH1A1 (0.38) ALDH1A1KDM4EPOLBCSNK1A1CLK4
SCHEMBL620246 0.78 CSNK1A1 (0.41) ALDH1A1KDM4EPOLBCSNK1A1CLK4
SCHEMBL31511514 0.78 CSNK1A1 (0.41) ALDH1A1KDM4EPOLBCSNK1A1CLK4
SCHEMBL8139272 0.78 KDM4E (0.40) ALDH1A1KDM4EPOLBCSNK1A1CLK4
SCHEMBL4424103 0.78 CSNK1A1 (0.46) ALDH1A1KDM4EPOLBCSNK1A1CLK4
SCHEMBL30826009 0.78 ALDH1A1 (0.40) ALDH1A1KDM4EPOLBCSNK1A1CLK4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117208902-A Preparation method and application of triazine-pyrazinyl nitrogen-rich nitrogen-doped porous carbon material 常州大学 2023-12-12 CN claimed
CN-113252800-A HPLC (high performance liquid chromatography) detection method for Pilarvir and related substances thereof and application of method 北京四环制药有限公司 2021-08-13 CN claimed
CN-112062728-A Synthetic method of 3, 5-dichloro-6-ethylpyrazine formamide 上海鑫凯化学科技有限公司 2020-12-11 CN claimed
US-12600732-B2 Bifunctional compounds for degrading BTK via ubiquitin proteosome pathway NURIX THERAPEUTICS, INC. (US) 2026-04-14 US disclosed
EP-4234030-B1 PD-1/PD-L1 INHIBITORS GILEAD SCIENCES INC (US) 2026-04-08 EP disclosed
US-12582722-B2 Bifunctional compounds for degrading BTK via ubiquitin proteosome pathway NURIX THERAPEUTICS, INC. (US) 2026-03-24 US disclosed
US-12583862-B2 Bifunctional compounds for degrading BTK via ubiquitin proteosome pathway NURIX THERAPEUTICS, INC. (US) 2026-03-24 US disclosed
US-12583852-B2 Heterocycle derivative JW PHARMACEUTICAL CORPORATION (KR) 2026-03-24 US disclosed
EP-4695238-A1 CDK2 INHIBITORS Blueprint Medicines Corporation (US) 2026-02-18 EP disclosed
US-20260035378-A1 BIFUNCTIONAL COMPOUNDS FOR DEGRADING BTK VIA UBIQUITIN PROTEOSOME PATHWAY NURIX THERAPEUTICS INC (US) 2026-02-05 US disclosed
US-20260001892-A1 COMPOUND FOR REGULATING AND CONTROLLING ACTIVITY OF 15-PGDH AND PREPARATION METHOD THEREFOR SCINNOHUB PHARMACEUTICAL CO LTD (CN) 2026-01-01 US disclosed
EP-2570415-A1 N-[4-(1h-pyrazolo[3,4-b]pyrazin-6-yl)-phenyl]-sulfonamides and their use as pharmaceuticals SANOFI (FR) 2013-03-20 EP disclosed
EP-2328890-B1 6 SUBSTITUTED 2-HETEROCYCLYLAMINO PYRAZINE COMPOUNDS AS CHK-1 INHIBITORS PFIZER (US) 2012-01-25 EP disclosed
EP-2328890-B1 6 SUBSTITUTED 2-HETEROCYCLYLAMINO PYRAZINE COMPOUNDS AS CHK-1 INHIBITORS PFIZER (US) 2012-01-25 EP disclosed
US-20110144084-A1 6 SUBSTITUTED 2- HETEROCYCLYLAMINO PYRAZINE COMPOUNDS AS CHK-1 INHIBITORS PFIZER INC (US) 2011-06-16 US disclosed
US-20110144084-A1 6 SUBSTITUTED 2- HETEROCYCLYLAMINO PYRAZINE COMPOUNDS AS CHK-1 INHIBITORS PFIZER INC (US) 2011-06-16 US disclosed
US-20110144084-A1 6 SUBSTITUTED 2- HETEROCYCLYLAMINO PYRAZINE COMPOUNDS AS CHK-1 INHIBITORS PFIZER INC (US) 2011-06-16 US disclosed
EP-2328890-A1 6 SUBSTITUTED 2-HETEROCYCLYLAMINO PYRAZINE COMPOUNDS AS CHK-1 INHIBITORS Pfizer Inc. (US) 2011-06-08 EP disclosed
WO-2010016005-A1 6 SUBSTITUTED 2-HETEROCYCLYLAMINO PYRAZINE COMPOUNDS AS CHK-1 INHIBITORS PFIZER INC. (US) 2010-02-11 WO disclosed
WO-2010016005-A1 6 SUBSTITUTED 2-HETEROCYCLYLAMINO PYRAZINE COMPOUNDS AS CHK-1 INHIBITORS PFIZER INC. (US) 2010-02-11 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 (7 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-12582722-B2 Bifunctional compounds for degrading BTK via ubiquitin proteosome pathway PSMB2, PSME3, PSMB3 ALDH1A1 4614/4885KDM4E 1543/4885POLB 1902/4885
US-20260001892-A1 COMPOUND FOR REGULATING AND CONTROLLING ACTIVITY OF 15-PGDH AND PREPARATION METHOD THEREFOR CYP11B1, HSD11B1, CYP11B2 ALDH1A1 114/4885KDM4E 3341/4885POLB 1275/4885
US-12583852-B2 Heterocycle derivative AR, SRD5A1, NR5A1 ALDH1A1 1733/4885KDM4E 413/4885POLB 4201/4885
US-20260035378-A1 BIFUNCTIONAL COMPOUNDS FOR DEGRADING BTK VIA UBIQUITIN PROTEOSOME PATHWAY BTK, PSMB2, PSMB1 ALDH1A1 4621/4885KDM4E 999/4885POLB 2338/4885
US-12583862-B2 Bifunctional compounds for degrading BTK via ubiquitin proteosome pathway BTK, PSMB2, PSME3 ALDH1A1 4714/4885KDM4E 810/4885POLB 2490/4885
US-12600732-B2 Bifunctional compounds for degrading BTK via ubiquitin proteosome pathway BTK, BCL9, BCL9L ALDH1A1 4642/4885KDM4E 530/4885POLB 3718/4885
US-20110144084-A1 6 SUBSTITUTED 2- HETEROCYCLYLAMINO PYRAZINE COMPOUNDS AS CHK-1 INHIBITORS CHKA, CSNK1A1, CHKB ALDH1A1 2651/4885KDM4E 1159/4885POLB 4595/4885

“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.