SCHEMBL2118007

SCHEMBL2118007

CCOc1nc(O)cc(O)n1

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 3/20 0.41
KMT2A Q03164 3/20 0.41
CYP1A2 P05177 1/20 0.41
POLB P06746 1/20 0.38
PDE4B Q07343 1/20 0.37
PDE4D Q08499 1/20 0.37
MAT2A P31153 1/20 0.36
MAPK1 P28482 1/20 0.36
SMN1; SMN2 Q16637 1/20 0.36
ALDH1A1 P00352 2/20 0.35
TSHR P16473 1/20 0.35
L3MBTL1 Q9Y468 1/20 0.35
MAPT P10636 2/20 0.35
LMNA P02545 1/20 0.35
NQO1 P15559 1/20 0.35
LTA4H P09960 1/20 0.34
HSD17B10 Q99714 1/20 0.34
PTGS1 P23219 1/20 0.34
PTGS2 P35354 1/20 0.34
HPGD P15428 1/20 0.33

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
SCHEMBL7776188 0.98 MEN1 (0.39) MEN1KMT2ACYP1A2POLBPDE4B
SCHEMBL11789798 0.87 SMN1; SMN2 (0.37) MEN1KMT2ACYP1A2POLBPDE4B
SCHEMBL11304283 0.86 MEN1 (0.35) MEN1KMT2ACYP1A2POLBPDE4B
SCHEMBL10852041 0.84 SMN1; SMN2 (0.39) MEN1KMT2ACYP1A2POLBPDE4B
SCHEMBL11728875 0.84 LMNA (0.40) MEN1KMT2ACYP1A2PDE4BPDE4D
SCHEMBL17584792 0.80 LTA4H (0.41) MEN1KMT2ASMN1; SMN2ALDH1A1L3MBTL1
SCHEMBL11443302 0.80 MEN1 (0.39) MEN1KMT2ACYP1A2POLBSMN1; SMN2
SCHEMBL582039 0.76 MEN1 (0.52) MEN1KMT2ACYP1A2POLBPDE4B
SCHEMBL10969660 0.76 MAPK8 (0.43) MEN1KMT2ACYP1A2POLBPDE4B
SCHEMBL11737692 0.76 LMNA (0.40) CYP1A2MAPK1SMN1; SMN2ALDH1A1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114262300-A Preparation method of 2-ethoxy-4, 6-difluoropyrimidine 浙江伟锋药业有限公司 2022-04-01 CN claimed
CN-111303045-A Production process of 2-ethoxy-4, 6-difluoropyrimidine 温州大学 2020-06-19 CN claimed
EP-1042303-B1 CHLOROPYRIMIDINE PROCESS DOW AGROSCIENCES LLC (US) 2003-02-05 EP claimed
EP-0603893-B1 Process for the preparation of 2-ethoxy-4,6-dihydroxy pyrimidin or their alkaline salts SUEDDEUTSCHE KALKSTICKSTOFF (DE) 2001-08-08 EP claimed
US-6066734-A Chloropyrimidine process DOW AGROSCIENCES LLC (US) 2000-05-23 US claimed
US-5552546-A Process for the preparation of 2-ethoxy-4,6-dihydroxypyrimidine DOWELANCO (US) 1996-09-03 US claimed
US-5463055-A Reacting O-ethylisourea (or salt) with an alcoholate and/or a malonic acid dialkyl ester derivative, then acidification, desalting SKW TROSTBERG AKTIENGESELLSCHAFT (DE) 1995-10-31 US claimed
EP-0603893-A1 Process for the preparation of 2-ethoxy-4,6-dihydroxy pyrimidin or their alkaline salts SKW Trostberg Aktiengesellschaft (DE) 1994-06-29 EP claimed
CN-114262300-A Preparation method of 2-ethoxy-4, 6-difluoropyrimidine 浙江伟锋药业有限公司 2022-04-01 CN disclosed
CN-114262300-A Preparation method of 2-ethoxy-4, 6-difluoropyrimidine 浙江伟锋药业有限公司 2022-04-01 CN disclosed
CN-106866547-B Synthesis method of 2-ethoxy-4, 6-dichloropyrimidine 江苏省农用激素工程技术研究中心有限公司 2020-11-10 CN disclosed
CN-111303045-A Production process of 2-ethoxy-4, 6-difluoropyrimidine 温州大学 2020-06-19 CN disclosed
US-8158787-B2 Process for producing trichloropyrimidine compound SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2012-04-17 US disclosed
US-20100160630-A1 PROCESS FOR PRODUCING TRICHLOROPYRIMIDINE COMPOUND SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2010-06-24 US disclosed
US-5463055-A Reacting O-ethylisourea (or salt) with an alcoholate and/or a malonic acid dialkyl ester derivative, then acidification, desalting SKW TROSTBERG AKTIENGESELLSCHAFT (DE) 1995-10-31 US disclosed
EP-0603893-A1 Process for the preparation of 2-ethoxy-4,6-dihydroxy pyrimidin or their alkaline salts SKW Trostberg Aktiengesellschaft (DE) 1994-06-29 EP disclosed
EP-0603893-A1 Process for the preparation of 2-ethoxy-4,6-dihydroxy pyrimidin or their alkaline salts SKW Trostberg Aktiengesellschaft (DE) 1994-06-29 EP disclosed
EP-0603893-A1 Process for the preparation of 2-ethoxy-4,6-dihydroxy pyrimidin or their alkaline salts SKW Trostberg Aktiengesellschaft (DE) 1994-06-29 EP disclosed
US-4059696-A INSECTICIDE, MITICIDE BAYER AKTIENGESELLSCHAFT (DT) 1977-11-22 US disclosed
US-4045561-A Pesticidal pyrimidinyl phosphorus esters SANDOZ LTD. (CH) 1977-08-30 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-20100160630-A1 PROCESS FOR PRODUCING TRICHLOROPYRIMIDINE COMPOUND DPYD, TYMP, TST MEN1 4481/4885KMT2A 3104/4885CYP1A2 777/4885

“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.