SCHEMBL3569140

SCHEMBL3569140

COC(=O)c1ccc(CN2CCNCC2)cc1

nearest known ligand 0.71

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CHKA P35790 1/20 0.60
KDM4E B2RXH2 1/20 0.59
SMN1; SMN2 Q16637 2/20 0.57
MAPK1 P28482 1/20 0.57
MEN1 O00255 4/20 0.55
KMT2A Q03164 4/20 0.55
MAPT P10636 3/20 0.55
GAA P10253 2/20 0.55
ALDH1A1 P00352 2/20 0.55
HPGD P15428 1/20 0.55
CHRM3 P20309 1/20 0.55
SYK P43405 1/20 0.54
OPRD1 P41143 1/20 0.52
ATM Q13315 1/20 0.52
L3MBTL1 Q9Y468 1/20 0.52
SIGMAR1 Q99720 1/20 0.51
CHRM2 P08172 1/20 0.51
CHRM1 P11229 1/20 0.51
ADRA2C P18825 1/20 0.51
CCR2 P41597 1/20 0.51

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
Hydrochloric Acid SCHEMBL19585072 0.98 CHKA (0.59) CHKAKDM4ESMN1; SMN2MAPK1MEN1
Hydrochloric Acid SCHEMBL10900610 0.98 CHKA (0.59) CHKAKDM4ESMN1; SMN2MAPK1MEN1
SCHEMBL5038790 0.98 CHKA (0.59) CHKAKDM4ESMN1; SMN2MAPK1MEN1
SCHEMBL3036998 0.94 CHKA (0.62) CHKAKDM4ESMN1; SMN2MAPK1MEN1
Hydrochloric Acid SCHEMBL20305004 0.93 CXCR4 (0.62) CHKAKDM4ESMN1; SMN2MAPK1MEN1
Tert-Butyl Formate SCHEMBL28272976 0.89 CHKA (0.50) CHKAKDM4ESMN1; SMN2MAPK1MEN1
SCHEMBL5026403 0.87 KDM4E (0.50) CHKAKDM4ESMN1; SMN2MAPK1MEN1
SCHEMBL2873979 0.86 CHKA (0.72) CHKAKDM4ESMN1; SMN2MAPK1MEN1
SCHEMBL20210248 0.86 CHKA (0.77) CHKAKDM4ESMN1; SMN2MAPK1MEN1
SCHEMBL10568920 0.85 LMNA (0.58) KDM4ESMN1; SMN2MAPK1MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105001205-A Preparation method of imatinib impurity D QILU TIANHE PHARMACEUTICAL CO LTD 2015-10-28 CN claimed
US-12629371-B2 Compositions and methods for inhibiting kinases INHIBIKASE THERAPEUTICS, INC. (US) 2026-05-19 US disclosed
US-20250250266-A1 COMPOSITIONS AND METHODS FOR INHIBITING KINASES INHIBIKASE THERAPEUTICS, INC. 2025-08-07 US disclosed
US-20250136614-A1 2,7-SUBSTITUTED PYRROLO[2,1-F][1,2,4]TRIAZINE COMPOUND HAVING PROTEIN KINASE INHIBITORY ACTIVITY MAGICBULLETTHERAPEUTICS CO., LTD. (KR) 2025-05-01 US disclosed
EP-4442691-A1 2,7-SUBSTITUTED PYRROLO[2,1-F][1,2,4]TRIAZINE COMPOUND HAVING PROTEIN KINASE INHIBITORY ACTIVITY Magicbullettherapeutics Co., Ltd. (KR) 2024-10-09 EP disclosed
CN-113072542-B ROR gamma t inhibitor and preparation method and application thereof 广东东阳光药业股份有限公司 2024-04-05 CN disclosed
US-11725005-B2 Compositions and methods for inhibiting kinases INHIBIKASE THERAPEUTICS, INC. (US) 2023-08-15 US disclosed
CN-116535343-A Hydroxamic acid compound and application thereof 温州医科大学 2023-08-04 CN disclosed
WO-2023140629-A1 2,7-SUBSTITUTED PYRROLO[2,1-F][1,2,4]TRIAZINE COMPOUND HAVING PROTEIN KINASE INHIBITORY ACTIVITY 닥터아이앤비(주) 2023-07-27 WO disclosed
WO-2023101387-A1 2,7-SUBSTITUTED PYRROLO[2,1-F][1,2,4]TRIAZINE COMPOUND HAVING PROTEIN KINASE INHIBITORY ACTIVITY 연세대학교 산학협력단 2023-06-08 WO disclosed
EP-1874315-A2 COMPOSITIONS OF NOVEL OPIOID COMPOUNDS AND METHOD OF USE THEREOF Mount Cook Biosciences, Inc. (US) 2008-01-09 EP disclosed
EP-1685094-A4 ACYLUREA CONNECTED AND SULFONYLUREA CONNECTED HYDROXAMATES S BIO PTE LTD (SG) 2007-08-22 EP disclosed
CN-1310911-C Piperazine benzothiazoles as therapeutics for cerebral ischemic and CNS disorders APPLIED RESEARCH SYSTEMS (AN) 2007-04-18 CN disclosed
US-20070043028-A1 Compositions of novel opioid compounds and method of use thereof DMK PHARMACEUTICALS CORPORATION 2007-02-22 US disclosed
WO-2006113468-A2 COMPOSITIONS OF NOVEL OPIOID COMPOUNDS AND METHOD OF USE THEREOF MOUNT COOK BIOSCIENCES, INC. (US) 2006-10-26 WO disclosed
EP-1685094-A1 ACYLUREA CONNECTED AND SULFONYLUREA CONNECTED HYDROXAMATES S*Bio Pte Ltd (SG) 2006-08-02 EP disclosed
CN-1662528-A Piperazine benzothiazoles as therapeutics for cerebral ischemic and CNS disorders APPLIED RESEARCH SYSTEMS (AN) 2005-08-31 CN disclosed
WO-2005040101-A1 ACYLUREA CONNECTED AND SULFONYLUREA CONNECTED HYDROXAMATES S*BIO PTE LTD (SG) 2005-05-06 WO disclosed
WO-2005040101-A1 ACYLUREA CONNECTED AND SULFONYLUREA CONNECTED HYDROXAMATES S*BIO PTE LTD (SG) 2005-05-06 WO disclosed
US-4616086-A ANTICOAGULANTS BOEHRINGER MANNHEIM GMBH (DE) 1986-10-07 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 (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-20250136614-A1 2,7-SUBSTITUTED PYRROLO[2,1-F][1,2,4]TRIAZINE COMPOUND HAVING PROTEIN KINASE INHIBITORY ACTIVITY STK25, MAP3K15, MAP3K5 CHKA 1403/4885KDM4E 2242/4885SMN1; SMN2 3150/4885
US-12629371-B2 Compositions and methods for inhibiting kinases PTK2, HCK, PTK2B CHKA 11/4885KDM4E 2732/4885SMN1; SMN2 1120/4885
US-20070043028-A1 Compositions of novel opioid compounds and method of use thereof OPRL1, OPRD1, OPRK1 CHKA 1366/4885KDM4E 3019/4885SMN1; SMN2 1087/4885
US-20250250266-A1 COMPOSITIONS AND METHODS FOR INHIBITING KINASES MAP3K1, PACSIN2, MAP3K3 CHKA 180/4885KDM4E 1589/4885SMN1; SMN2 4333/4885
US-11725005-B2 Compositions and methods for inhibiting kinases MAP3K1, PACSIN2, MAP3K3 CHKA 180/4885KDM4E 1589/4885SMN1; SMN2 4333/4885

“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.