SCHEMBL319105

SCHEMBL319105

O=C(O)c1ccnc(Cl)n1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 7/20 0.53
KDM5A P29375 2/20 0.53
KDM3A Q9Y4C1 2/20 0.53
JMJD1C Q15652 1/20 0.53
ALOX15 P16050 2/20 0.48
TSHR P16473 1/20 0.48
ACMSD Q8TDX5 1/20 0.48
TDP1 Q9NUW8 1/20 0.48
KMO O15229 3/20 0.46
ALDH1A1 P00352 4/20 0.45
KDM6B O15054 1/20 0.45
TET3 O43151 1/20 0.45
KDM4A O75164 1/20 0.45
BBOX1 O75936 1/20 0.45
MAPT P10636 1/20 0.45
KDM5C P41229 1/20 0.45
ASPH Q12797 1/20 0.45
KDM4D Q6B0I6 1/20 0.45
TET2 Q6N021 1/20 0.45
ALKBH5 Q6P6C2 1/20 0.45

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 SCHEMBL8880890 0.98 KDM4E (0.52) KDM4EKDM5AKDM3AJMJD1CALOX15
(Chloromethyl)Benzene SCHEMBL27882366 0.85 KDM4E (0.41) KDM4EKDM5AKDM3AJMJD1CALOX15
SCHEMBL2046174 0.83 KDM4E (0.38) KDM4EKDM5AKDM3AJMJD1CALOX15
SCHEMBL3053770 0.83 LMNA (0.39) KDM4EKDM5AKDM3AJMJD1CKMO
SCHEMBL2012751 0.81 ALDH1A1 (0.45) KDM4EKDM5AKDM3AJMJD1CKMO
SCHEMBL2894784 0.81 LMNA (0.57) KDM4EKDM5AKDM3AJMJD1CTSHR
SCHEMBL1505808 0.77 KDM4E (0.57) KDM4EKDM5AKDM3AJMJD1CALOX15
SCHEMBL24369081 0.76 MAPT (0.39) KDM4EKDM5AKDM3AJMJD1CTDP1
SCHEMBL18824618 0.76 ALDH1A1 (0.39) KDM4EALOX15ALDH1A1KDM4AMAPT
SCHEMBL1427770 0.76 RAB9A (0.43) MAPTLMNASMN1; SMN2HPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119775207-A Morpholine-containing amide compound and preparation method and application thereof 山东农业大学 2025-04-08 CN claimed
CN-111393376-B Synthetic method of 2-chloropyrimidine-4-formic acid 安徽赛迪生物科技有限公司 2022-05-13 CN claimed
CN-112979559-A 2-phenyl pyrimidine formic acid derivative and preparation method and application thereof 沈阳药科大学 2021-06-18 CN claimed
WO-2021103256-A1 CONTINUOUS SYNTHESIS METHOD FOR 2-CHLOROPYRIMIDINE-4-FORMIC ACID COMPOUND 天津凯莱英制药有限公司 2021-06-03 WO claimed
CN-111393376-A Synthetic method of 2-chloropyrimidine-4-formic acid 安徽赛迪生物科技有限公司 2020-07-10 CN claimed
CN-110642789-B Continuous synthesis method of 2-chloropyrimidine-4-formic acid compound 天津凯莱英制药有限公司 2020-05-26 CN claimed
CN-110642789-A Continuous synthesis method of 2-chloropyrimidine-4-formic acid compound 天津凯莱英制药有限公司 2020-01-03 CN claimed
CN-106083734-A A kind of method preparing 2 chloropyrimide 4 formic acid 安徽赛迪生物科技有限公司 2016-11-09 CN claimed
US-5591853-A CHEMICAL INTERMEDIATE PRODUCTS FOR PHARMACEUTICALS LONZA LTD. (CH) 1997-01-07 US claimed
EP-0552760-A1 Microbiological process for the preparation of 2-halopyrimidine-4-carboxylic acids LONZA AG (CH) 1993-07-28 EP claimed
JP-5306273-A None JP disclosed
US-20260098044-A1 TRICYCLIC HETEROARYL COMPOUNDS AS INHIBITORS OF TYK2 AND/OR JAK1 INCYTE CORP (US) 2026-04-09 US disclosed
US-20260078113-A1 HETEROCYCLIC COMPOUNDS AS IMMUNOMODULATORS INCYTE CORP (US) 2026-03-19 US disclosed
US-12577229-B2 Substituted {5-methoxy-6-[(5-methoxypyridin-2-yl)methoxy]pyridin-3-yl} methyl compounds as CSF-1R inhibitors ELI LILLY AND COMPANY (US) 2026-03-17 US disclosed
WO-2026047630-A1 HETEROCYCLIC COMPOUNDS AS EGFR INHIBITORS HETERO LABS LIMITED (IN) 2026-03-05 WO disclosed
WO-1999002501-A1 NOVEL COMPOUNDS ASTRA PHARMACEUTICALS LTD. (GB) 1999-01-21 WO disclosed
US-5591853-A CHEMICAL INTERMEDIATE PRODUCTS FOR PHARMACEUTICALS LONZA LTD. (CH) 1997-01-07 US disclosed
US-5591853-A CHEMICAL INTERMEDIATE PRODUCTS FOR PHARMACEUTICALS LONZA LTD. (CH) 1997-01-07 US disclosed
JP-H05306273-A MICROBIOLOGICAL PRODUCTION OF 2-HALO-PYRIMIDINE-4-CARBOXYLIC ACID LONZA AG 1993-11-19 JP disclosed
EP-0552760-A1 Microbiological process for the preparation of 2-halopyrimidine-4-carboxylic acids LONZA AG (CH) 1993-07-28 EP 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 (3 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-12577229-B2 Substituted {5-methoxy-6-[(5-methoxypyridin-2-yl)methoxy]pyridin-3-yl} methyl compounds as CSF-1R inhibitors CSF1R, CSF3R, AGER KDM4E 348/4885KDM5A 191/4885KDM3A 295/4885
US-20260078113-A1 HETEROCYCLIC COMPOUNDS AS IMMUNOMODULATORS MSR1, NR3C1, CCR1 KDM4E 4270/4885KDM5A 4023/4885KDM3A 3750/4885
US-20260098044-A1 TRICYCLIC HETEROARYL COMPOUNDS AS INHIBITORS OF TYK2 AND/OR JAK1 JAK1, TYK2, JAK2 KDM4E 1764/4885KDM5A 2020/4885KDM3A 1049/4885

“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.