SCHEMBL191344

SCHEMBL191344

Cc1cc(O)c(C(=O)O)cn1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GABRP O00591 2/20 0.48
GABRD O14764 2/20 0.48
GABRA1 P14867 2/20 0.48
GABRB1 P18505 2/20 0.48
GABRG2 P18507 2/20 0.48
GABRB3 P28472 2/20 0.48
GABRA5 P31644 2/20 0.48
GABRA3 P34903 2/20 0.48
GABRA2 P47869 2/20 0.48
GABRB2 P47870 2/20 0.48
GABRA4 P48169 2/20 0.48
GABRE P78334 2/20 0.48
GABRA6 Q16445 2/20 0.48
GABRG1 Q8N1C3 2/20 0.48
GABRG3 Q99928 2/20 0.48
GABRQ Q9UN88 2/20 0.48
CSNK2A1 P68400 1/20 0.44
LDHA P00338 1/20 0.43
KDM4E B2RXH2 5/20 0.43
KMT2A Q03164 1/20 0.43

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 SCHEMBL11589303 0.98 GABRP (0.47) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL27724461 0.89 GABRP (0.41) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL7018427 0.83 CSNK2A1 (0.48) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL5782203 0.83 GABRP (0.52) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL15632532 0.82 SPR (0.40) MAPTGAA
SCHEMBL8626851 0.82 NNMT (0.47) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL8626848 0.82 GABRP (0.35) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL6664673 0.82 GABRP (0.35) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL1436086 0.81 GABRP (0.66) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL31043801 0.81 GABRP (0.66) GABRPGABRDGABRA1GABRB1GABRG2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2723882-B1 PROCESS FOR PREPARING 3'-THIOSUBSTITUTED CEPHALOSPORINS EMPLOYING A PENICILLIN G ACYLASE CENTRIENT PHARMACEUTICALS NETHERLANDS B V (NL) 2019-05-01 EP claimed
CN-103497151-B Synthetic method of 4-amidogen-6-methylnicotinicacid SHANDONG BOYUAN PHARMACEUTICAL CO LTD 2015-07-15 CN claimed
CN-103635585-A Process for preparing 3'-thiosubstituted cephalosporins employing a penicillin G acylase DSM SINOCHEM PHARM NL BV 2014-03-12 CN claimed
CN-103497151-A Synthetic method of 4-amidogen-6-methylnicotinicacid SHANDONG BOYUAN PHARMACEUTICAL CO LTD 2014-01-08 CN claimed
CN-101759634-B Composite method for cefpiramide midbody D-alpha-(4-Hydroxy-6-methylnicotinamido) hydroxyphenylacetic acid SHANDONG ZHONGCHENG PHARMACEUTICAL CO LTD 2011-02-16 CN claimed
CN-101293868-B Process for synthesizing D-alpha-(6-methyl-4-hydroxyl nicotinamide base)p-hydroxyphenylacetic acid QILU ANTIBIOTICS PHARMACEUTICA CO LTD 2010-11-10 CN claimed
CN-101759634-A Composite method for cefpiramide midbody D-alpha-(4-Hydroxy-6-methylnicotinamido) hydroxyphenylacetic acid SHANDONG ZHONGCHENG PHARMACEUT 2010-06-30 CN claimed
CN-101293868-A Process for synthesizing D-alpha-(6-methyl-4-hydroxyl nicotinamide base)p-hydroxyphenylacetic acid QILU ANTIBIOTICS PHARMACEUTICA (CN) 2008-10-29 CN claimed
JP-57126477-A None JP disclosed
JP-55049385-A None JP disclosed
JP-54125678-A None JP disclosed
US-20260138991-A1 SEMI-SATURATED BICYCLIC DERIVATIVES AND RELATED USES MOMA THERAPEUTICS INC (US) 2026-05-21 US disclosed
EP-4294804-B1 PYRIDONE COMPOUNDS AND METHODS OF USE EXELIXIS INC (US) 2026-04-08 EP disclosed
EP-4705298-A2 SEMI-SATURATED BICYCLIC DERIVATIVES AND RELATED USES Moma Therapeutics, Inc. (US) 2026-03-11 EP disclosed
EP-1737451-A2 MONOCYCLIC HETEROCYCLES AS KINASE INHIBITORS Bristol-Myers Squibb Company (US) 2007-01-03 EP disclosed
WO-2005117867-A2 MONOCYCLIC HETEROCYCLES AS KINASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2005-12-15 WO disclosed
US-20050245530-A1 Monocyclic heterocycles as kinase inhibitors BRISTOL-MYERS SQUIBB COMPANY 2005-11-03 US disclosed
JP-S57126477-A PREPARATION OF NICOTINIC ACID DERIVATIVE KAWAKEN FINE CHEM CO LTD 1982-08-06 JP disclosed
JP-S5549385-A NOVEL ANTIBACTERIAL COMPOUND YAMANOUCHI PHARMACEUT CO LTD 1980-04-09 JP disclosed
JP-S54125678-A PREPARATION OF 4-HYDROXY-6-METHYLNICOTINIC ACID YAMANOUCHI PHARMACEUT CO LTD 1979-09-29 JP 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-20260138991-A1 SEMI-SATURATED BICYCLIC DERIVATIVES AND RELATED USES POLA1, SUB1, CTDSP1 GABRP 2474/4885GABRD 3001/4885GABRA1 2208/4885
US-20050245530-A1 Monocyclic heterocycles as kinase inhibitors CDK2, MAP3K19, CDK1 GABRP 3718/4885GABRD 3935/4885GABRA1 3587/4885

“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.