SCHEMBL63857

SCHEMBL63857

O=C(O)c1cnc(Cl)nc1

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NAPRT Q6XQN6 1/20 0.58
ALDH1A1 P00352 2/20 0.52
HSD17B10 Q99714 2/20 0.52
ALOX15 P16050 2/20 0.52
KDM4E B2RXH2 1/20 0.52
P4HA1 P13674 2/20 0.50
P4HTM Q9NXG6 2/20 0.50
HCAR2 Q8TDS4 2/20 0.50
MIF P14174 1/20 0.48
GABRP O00591 1/20 0.46
GABRD O14764 1/20 0.46
GABRA1 P14867 1/20 0.46
GABRB1 P18505 1/20 0.46
GABRG2 P18507 1/20 0.46
GABRB3 P28472 1/20 0.46
GABRA5 P31644 1/20 0.46
GABRA3 P34903 1/20 0.46
GABRA2 P47869 1/20 0.46
GABRB2 P47870 1/20 0.46
GABRA4 P48169 1/20 0.46

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
SCHEMBL4886683 0.80 ALDH1A1 (0.58) NAPRTALDH1A1HSD17B10ALOX15KDM4E
SCHEMBL6987829 0.79 NAPRT (0.46) NAPRTP4HA1P4HTMMIFTP53
SCHEMBL1735166 0.78 RXRA (0.55) NAPRTALOX15TSHRTP53
SCHEMBL1968189 0.77 NNMT (0.50) NAPRTHSD17B10KDM4ECYP2C19TSHR
SCHEMBL600134 0.77 NAPRT (0.40) NAPRTALDH1A1HSD17B10ALOX15KDM4E
SCHEMBL27962218 0.77 NAPRT (0.41) NAPRTALDH1A1HSD17B10ALOX15KDM4E
SCHEMBL665987 0.77 JUN (0.47) ALDH1A1HPGDTSHRJUNNFKB1
SCHEMBL185448 0.76 ALDH1A1 (0.54) NAPRTALDH1A1HSD17B10ALOX15KDM4E
SCHEMBL3705899 0.76 ALDH1A1 (0.54) NAPRTALDH1A1HSD17B10ALOX15KDM4E
SCHEMBL26987992 0.75 ALDH1A1 (0.58) ALDH1A1ALOX15HPGDNFKB1NFKB2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117700369-A Preparation method of 2- (2-chloropyrimidine-5-yl) acetic acid/ester 上海彩迩文生化科技有限公司 2024-03-15 CN claimed
CN-109467536-B Synthesis method of 2-chloro/hydroxypyrimidine-5-carboxylic acid 沧州普瑞东方科技有限公司 2020-06-05 CN claimed
CN-105683202-B Boric acid compound SYNTRIX生物系统公司 2019-05-10 CN claimed
CN-109467536-A 2- chlorine/hydroxy pyrimidine -5- carboxylic acid synthetic method 沧州普瑞东方科技有限公司 2019-03-15 CN claimed
CN-105683202-A 2- [5- [ N- (4-fluorophenyl) carbamoyl ] pyrimidin-2-ylmethylsulfanylmethyl ] -4- (trifluoromethoxy) phenyl ] boronic acid SYNTRIX生物系统公司 2016-06-15 CN claimed
EP-3027627-A1 2- [5- [N- (4 -FLUOROPHENYL) CARBAMOYL]PYRIMIDIN- 2 - YLSULFANYLMETHYL]-4- (TRIFLUOROMET HOXY) PHENYL]BORONIC ACID Syntrix Biosystems, Inc. (US) 2016-06-08 EP claimed
CN-104844573-A Miazines BTK inhibitor, preparation method and medical application thereof UNIV CHINA PHARMA 2015-08-19 CN claimed
US-8969365-B2 Thiopyrimidinecarboxamides as CXCR1/2 modulators SYNTRIX BIOSYSTEMS, INC. (US) 2015-03-03 US claimed
US-20150038461-A1 THIOPYRIMIDINECARBOXAMIDES AS CXCR1/2 MODULATORS SYNTRIX BIOSYSTEMS, INC. (US) 2015-02-05 US claimed
WO-2015016938-A1 2- [5- [N- (4 -FLUOROPHENYL) CARBAMOYL] PYRIMIDIN- 2 - YLSULFANYLMETHYL] -4- (TRIFLUOROMET HOXY) PHENYL] BORONIC ACID SYNTRIX BIOSYSTEMS, INC. (US) 2015-02-05 WO claimed
CN-103664796-A Synthesis method of 5-[2-(5-carboxyl-pyrimidyl)]-1,3-benzene dicarboxylic acid UNIV LIAONING NORMAL 2014-03-26 CN claimed
CN-116406355-B P38 alpha mitogen-activated protein kinase inhibitors GEN1E生命科学公司 2026-05-15 CN disclosed
WO-2026087442-A1 AMINO-IMIDAZOLE ANTIBACTERIAL COMPOUNDS F. HOFFMANN-LA ROCHE AG (CH) 2026-04-30 WO disclosed
EP-4100410-B1 MUSCARINIC RECEPTOR 4 ANTAGONISTS AND METHODS OF USE NEUROCRINE BIOSCIENCES INC (US) 2026-04-22 EP disclosed
EP-4540267-B1 CYCLIC PEPTIDES FOR TRAPPING INTERLEUKIN-1 BETA MERCK SHARP & DOHME LLC (US) 2026-04-15 EP disclosed
WO-2006049681-A2 SELECTIVE NEUROPEPTIDE Y2 RECEPTOR AGONISTS BAYER PHARMACEUTICALS CORPORATION (US) 2006-05-11 WO disclosed
WO-2006048297-A1 PROCESS FOR THE PRODUCTION OF PYRIMIDINE-5-CARBOXYLATES LONZA AG (CH) 2006-05-11 WO disclosed
WO-2006018284-A1 COMPOUNDS AND COMPOSITIONS USEFUL AS CATHEPSIN S INHIBITORS NOVARTIS AG (CH) 2006-02-23 WO disclosed
WO-2006010750-A1 SUBSTITUTED INDOLYL ALKYL AMINO DERIVATIVES AS NOVEL INHIBITORS OF HISTONE DEACETYLASE JANSSEN PHARMACEUTICA N.V. (BE) 2006-02-02 WO disclosed
CN-1549717-A Cysteine protease inhibitors having 2-cyano-4-aminopyrimidine structure and cathepsin K inhibitory activity for the treatment of inflammation and other diseases ��˹��ŵ�� 2004-11-24 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-20150038461-A1 THIOPYRIMIDINECARBOXAMIDES AS CXCR1/2 MODULATORS CXCR1, CXCR5, CXCR2 NAPRT 491/4885ALDH1A1 1648/4885HSD17B10 3653/4885

“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.