SCHEMBL4921789

SCHEMBL4921789

CCOC(=O)c1ncncn1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 2/20 0.46
TSHR P16473 1/20 0.45
CYP2C9 P11712 1/20 0.44
CYP2C19 P33261 1/20 0.44
CA12 O43570 3/20 0.42
CA1 P00915 3/20 0.42
CA2 P00918 3/20 0.42
CA7 P43166 3/20 0.42
CA9 Q16790 3/20 0.42
CA14 Q9ULX7 3/20 0.42
ESR1 P03372 1/20 0.42
ESR2 Q92731 1/20 0.42
KDM4E B2RXH2 1/20 0.42
CDC7 O00311 1/20 0.41
DBF4 Q9UBU7 1/20 0.41
NR1H2 P55055 1/20 0.41
NR1H3 Q13133 1/20 0.41
LMNA P02545 1/20 0.41
CYP3A4 P08684 1/20 0.41
MAOA P21397 1/20 0.41

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
SCHEMBL28414475 0.82 CES2 (0.50) TSHRKDM4ELMNAKMT2AMEN1
SCHEMBL489524 0.81 TSHR (0.52) CYP1A2TSHRCA12CA1CA2
SCHEMBL12457581 0.79 CYP1A2 (0.46) CYP1A2TSHRCYP2C9CYP2C19CA12
Bromide SCHEMBL28533203 0.79 TSHR (0.50) CYP1A2TSHRCA12CA1CA2
SCHEMBL9271700 0.78 ALDH1A1 (0.45) TSHRCA12CA1CA2CA9
SCHEMBL12523424 0.78 CYP1A2 (0.44) CYP1A2TSHRCYP2C9CYP2C19CA12
SCHEMBL4921787 0.77 CYP1A2 (0.41) CYP1A2TSHRCYP2C9CYP2C19CA12
SCHEMBL31214229 0.76 KMT2A (0.48) CYP1A2TSHRCYP2C9CYP2C19CA12
SCHEMBL15260359 0.76 HTT (0.44) CYP1A2TSHRCYP2C9CYP2C19CA12
SCHEMBL12228825 0.76 CYP1A2 (0.52) CYP1A2TSHRKDM4ELMNACYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117412959-A Substituted 1-aryl-1 '-heteroaryl compounds, substituted 1,1' -biaryl compounds, and methods of use thereof 爱彼特生物制药公司 2024-01-16 CN disclosed
CN-117164499-A Substituted benzofurans, benzopyrroles, benzothiophenes and structurally related complement inhibitors 拜奥克里斯特制药公司 2023-12-05 CN disclosed
CN-116836184-A Preparation and application of Wee1 kinase inhibitor 药雅科技(上海)有限公司 2023-10-03 CN disclosed
CN-112272553-B Substituted benzofurans, benzopyrroles, benzothiophenes and structurally related complement inhibitors 拜奥克里斯特制药公司 2023-09-22 CN disclosed
CN-115413275-A Substituted 1,1 , -biphenyl compounds and methods of use thereof 爱彼特生物制药公司 2022-11-29 CN disclosed
CN-113767100-A Bicyclic heteroaryl compounds and uses thereof 锐新医药公司 2021-12-07 CN disclosed
CN-112272553-A Substituted benzofurans, benzopyrrole, benzothiophenes and structurally related complement inhibitors 拜奥克里斯特制药公司 2021-01-26 CN disclosed
CN-108026105-B TGF-beta receptor antagonists 百时美施贵宝公司 2020-10-16 CN disclosed
CN-109928976-A A kind of method of industrialized production EOC317 泰州亿腾景昂药业有限公司 2019-06-25 CN disclosed
CN-1993130-B Processes and intermediates used for preparing fused heterocyclic kinase inhibitors BRISTOL MYERS SQUIBB CO 2010-06-23 CN disclosed
CN-101723948-A C-6 modified indazolylpyrrolotriazines BRISTOL MYERS SQUIBB CO 2010-06-09 CN disclosed
CN-101365454-A Substituted 4-amino-pyrrolotriazine derivatives for the treatment of hyperproliferative disorders and diseases associated with angiogenesis BAYER HEALTHCARE LLC (US) 2009-02-11 CN disclosed
US-20080200475-A1 4-Piperazinothieno[2,3-D] Pyrimidine Compounds As Platelet Aggregation Inhibitors PFIZER INC. 2008-08-21 US disclosed
EP-1866317-A1 4-PIPERAZINOTHIENO [2, 3-D] PYRIMIDINE COMPOUNDS AS PLATELET AGGREGATION INHIBITORS Pharmacia & Upjohn Company LLC (US) 2007-12-19 EP disclosed
CN-1993130-A Processes and intermediates useful for preparing fused heterocyclic kinase inhibitors BRISTOL MYERS SQUIBB CO (US) 2007-07-04 CN disclosed
WO-2006103555-A1 4-PIPERAZINOTHIENO [2, 3-D] PYRIMIDINE COMPOUNDS AS PLATELET AGGREGATION INHIBITORS PHARMACIA & UPJOHN COMPANY LLC (US) 2006-10-05 WO disclosed
CN-1726216-A C-6 modified indazolylpyrrolotriazines BRISTOL MYERS SQUIBB CO (US) 2006-01-25 CN 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-20080200475-A1 4-Piperazinothieno[2,3-D] Pyrimidine Compounds As Platelet Aggregation Inhibitors PF4, TBXA2R, P2RY4 CYP1A2 578/4885TSHR 337/4885CYP2C9 648/4885

“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.