SCHEMBL4067918

SCHEMBL4067918

Brc1c[nH]c2cncnc12

nearest known ligand 0.41

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
MAPK1 P28482 1/20 0.41
CCNT1 O60563 1/20 0.35
PIM1 P11309 1/20 0.35
CDK9 P50750 1/20 0.35
HASPIN Q8TF76 1/20 0.35
MAPK14 Q16539 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
SCHEMBL8820853 0.75 AURKA (0.34) MAPK14
SCHEMBL28103741 0.75 GRM4 (0.36) MAPK14
SCHEMBL2619212 0.75 PIM1 (0.34) PIM1MAPK14
SCHEMBL16652137 0.73 GSK3B (0.37) MAPK1PIM1
SCHEMBL11947207 0.71 DGAT1 (0.30)
SCHEMBL4325438 0.71 CCNT1 (0.40) CCNT1CDK9HASPIN
SCHEMBL13153053 0.71 HTR6 (0.31)
SCHEMBL2611062 0.71 FFAR1 (0.30)
SCHEMBL13725532 0.71 CCNT1 (0.40) CCNT1CDK9HASPIN
Hydrochloric Acid SCHEMBL5047877 0.69 CCNT1 (0.39) CCNT1CDK9HASPIN

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025119184-A1 SUBSTITUTED POLYCYCLIC COMPOUND 首药控股(北京)股份有限公司 2025-06-12 WO disclosed
WO-2021083438-A1 INHIBITORS OF PURINE NUCLEOSIDE PHOSPHORYLASE - SYNTHESIS AND USE THEREOF FOR TREATMENT OF T-CELL ACUTE LYMPHOBLASTIC LEUKEMIA AND LYMPHOMA USTAV ORGANICKE CHEMIE A BIOCHEMIE AV CR, V. V. I. (CZ) 2021-05-06 WO disclosed
CN-103958510-B For treating the Pyrrolopyrimidine compounds of cancer 北卡罗来纳大学教堂山分校 2016-10-19 CN disclosed
CN-103958510-A Pyrrolopyrimidine compounds for the treatment of cancer UNIV NORTH CAROLINA 2014-07-30 CN disclosed
CN-101062928-B Process for preparing 2-pyrrolidinyl-1h-pyrrolo[3,2-d]pyrimidine inhibitors of nucleoside metabolism IND RES LTD 2010-10-06 CN disclosed
EP-2077268-A1 Process for preparing inhibitors of nucleoside metabolism Industrial Research Limited (NZ) 2009-07-08 EP disclosed
EP-1165564-B1 PROCESS FOR PREPARING INHIBITORS OF NUCLEOSIDE METABOLISM IND RES LTD (NZ) 2009-03-11 EP disclosed
US-7405297-B2 Process for preparing inhibitors of nucleoside metabolism INDUSTRIAL RESEARCH LIMITED (NZ) 2008-07-29 US disclosed
CN-101062928-A Process for preparing 2-pyrrolidinyl-1h-pyrrolo[3,2-d]pyrimidine inhibitors of nucleoside metabolism IND RES LTD (NZ) 2007-10-31 CN disclosed
CN-100344630-C 3H, 5H-pyrrolo [3, 2-d ] pyrimidin-4-one derivatives and process for producing the same IND RES LTD (NZ) 2007-10-24 CN disclosed
US-20060089498-A1 Process for preparing inhibitors of nucleoside metabolism BIOCRYST PHARMACEUTICALS, INC. 2006-04-27 US disclosed
US-7022852-B2 Process for preparing inhibitors of nucleoside metabolism INDUSTRIAL RESEARCH LIMITED (NZ) 2006-04-04 US disclosed
CN-1727341-A 3H, 5H-pyrrolo [3, 2-d ] pyrimidin-4-one derivatives and process for producing the same IND RES LTD (NZ) 2006-02-01 CN disclosed
CN-1196704-C Process for preparing nucleoside metabolism inhibitor and intermediate compound IND RES LTD (NZ) 2005-04-13 CN disclosed
US-20040181063-A1 Process for preparing inhibitors of nucleoside metabolism BIOCRYST PHARMACEUTICALS, INC. 2004-09-16 US disclosed
US-6693193-B1 COUPLING AN N- AND O-PROTECTED 2,3-DIHYDROXY-PYRROLIDINE TO THE 2-POSITION AND DEPROTECTING INDUSTRIAL RESEARCH LIMITED (NZ) 2004-02-17 US disclosed
EP-1165564-A4 PROCESS FOR PREPARING INHIBITORS OF NUCLEOSIDE METABOLISM IND RES LTD (NZ) 2003-01-22 EP disclosed
CN-1370171-A Process for preparing nucleoside metabolism inhibitors IND RES LTD (NZ) 2002-09-18 CN disclosed
EP-1165564-A2 PROCESS FOR PREPARING INHIBITORS OF NUCLEOSIDE METABOLISM INDUSTRIAL RESEARCH LIMITED (NZ) 2002-01-02 EP disclosed
WO-2000061783-A2 PROCESS FOR PREPARING INHIBITORS OF NUCLEOSIDE METABOLISM INDUSTRIAL RESEARCH LIMITED (NZ) 2000-10-19 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 (2 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-20060089498-A1 Process for preparing inhibitors of nucleoside metabolism UGT1A3, AGL, PNP MAPK1 2046/4885CCNT1 879/4885PIM1 4647/4885
US-20040181063-A1 Process for preparing inhibitors of nucleoside metabolism XDH, PNP, AGL MAPK1 1320/4885CCNT1 715/4885PIM1 4705/4885

“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.