SCHEMBL197024

SCHEMBL197024

O=C(O)C(O)c1cccnc1

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.60
LMNA P02545 3/20 0.59
MAPK1 P28482 1/20 0.59
CFTR P13569 1/20 0.53
SLC6A2 P23975 1/20 0.53
SLC6A4 P31645 1/20 0.53
SLC6A3 Q01959 1/20 0.53
GOPC Q9HD26 1/20 0.53
KDM4E B2RXH2 1/20 0.50
GRM8 O00222 1/20 0.49
GRM4 Q14833 1/20 0.49
GAA P10253 2/20 0.48
ALDH1A1 P00352 1/20 0.48
APP P05067 1/20 0.48
HCAR3 P49019 1/20 0.48
HCAR2 Q8TDS4 1/20 0.48
TBXAS1 P24557 1/20 0.47
L3MBTL1 Q9Y468 1/20 0.47
KCNN4 O15554 2/20 0.47
KCNA5 P22460 2/20 0.47

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
SCHEMBL10170624 1.00 SMN1; SMN2 (0.60) SMN1; SMN2LMNAMAPK1CFTRSLC6A2
SCHEMBL2684159 1.00 SMN1; SMN2 (0.60) SMN1; SMN2LMNAMAPK1CFTRSLC6A2
SCHEMBL31404936 1.00 SMN1; SMN2 (0.60) SMN1; SMN2LMNAMAPK1CFTRSLC6A2
Sulfuric Acid SCHEMBL6228059 0.93 SMN1; SMN2 (0.53) SMN1; SMN2LMNAMAPK1CFTRSLC6A2
Mandelic Acid SCHEMBL810372 0.83 ALDH1A1 (0.68) SMN1; SMN2LMNAMAPK1GAAALDH1A1
SCHEMBL3135737 0.82 SMN1; SMN2 (0.53) SMN1; SMN2LMNACFTRSLC6A2SLC6A4
SCHEMBL14828702 0.82 SMN1; SMN2 (0.53) SMN1; SMN2LMNACFTRSLC6A2SLC6A4
SCHEMBL28049857 0.82 SMN1; SMN2 (0.53) SMN1; SMN2LMNACFTRSLC6A2SLC6A4
SCHEMBL29658816 0.82 SMN1; SMN2 (0.53) SMN1; SMN2LMNACFTRSLC6A2SLC6A4
SCHEMBL3103512 0.82 SMN1; SMN2 (0.53) SMN1; SMN2LMNACFTRSLC6A2SLC6A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0000560-B1 PROCESS FOR THE PREPARATION OF OPTICALLY ACTIVE ALPHA-HYDROXYCARBOXYLIC ACIDS F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1982-02-03 EP claimed
US-4204044-A SELECTIVE ASYMMETRIC, ENZYMATIC DEHYDROGENATIKN USING STREPTOMYCES, PSEUDOMONAS, BACILLUS OR CORYNEFORM MICROORGANISMS HOFFMANN-LA ROCHE INC. (US) 1980-05-20 US claimed
JP-8205878-A None JP disclosed
US-12122778-B2 Activating pyruvate kinase R NOVO NORDISK HEALTH CARE AG (CH) 2024-10-22 US disclosed
EP-3852791-B1 ACTIVATING PYRUVATE KINASE R NOVO NORDISK HEALTHCARE AG (CH) 2024-07-03 EP disclosed
US-20240182465-A1 FUSED RING SUBSTITUTED SIX-MEMBERED HETEROCYCLIC COMPOUND, PREPARATION METHOD THEREFOR AND USE THEREOF GENFLEET THERAPEUTICS (SHANGHAI) INC. (CN) 2024-06-06 US disclosed
EP-4303216-A1 FUSED RING SUBSTITUTED SIX-MEMBERED HETEROCYCLIC COMPOUND, PREPARATION METHOD THEREFOR AND USE THEREOF Genfleet Therapeutics (Shanghai) Inc. (CN) 2024-01-10 EP disclosed
CN-116981661-A Condensed ring substituted six-membered heterocyclic compound, preparation method and application thereof 劲方医药科技(上海)有限公司 2023-10-31 CN disclosed
WO-2023131122-A1 FUSED RING-SUBSTITUTED SIX-MEMBERED HETEROCYCLIC COMPOUND, AND PREPARATION METHOD THEREFOR AND USE THEREOF 劲方医药科技(上海)有限公司 2023-07-13 WO disclosed
US-20230055923-A1 ACTIVATING PYRUVATE KINASE R NOVO NORDISK HEALTH CARE AG (CH) 2023-02-23 US disclosed
US-20230055923-A1 ACTIVATING PYRUVATE KINASE R NOVO NORDISK HEALTH CARE AG (CH) 2023-02-23 US disclosed
US-5519132-A ALZHEIMER*S DISEASE, NERVOUS SYSTEM DISORDERS, PROMOTE RELEASE OF ACETYLCHOLINE THE DU PONT MERCK PHARMACEUTICAL COMPANY (US) 1996-05-21 US disclosed
US-5428035-A Enhance the release of neurotransmitter acetylcholine and useful for treating alzheimer's disease and cognition activator THE DUPONT MERCK PHARMACEUTICAL COMPANY (US) 1995-06-27 US disclosed
WO-1994007891-A1 1-SUBSTITUTED OXINDOLES AND AZAOXINDOLES AS NOVEL COGNITION ENHANCERS THE DU PONT MERCK PHARMACEUTICAL COMPANY (US) 1994-04-14 WO disclosed
US-5296478-A 1-substituted oxindoles as cognition enhancers THE DUPONT MERCK PHARMACEUTICAL CO. (US) 1994-03-22 US disclosed
US-4606756-A Herbicidal 2-(nitrogen heterocycle)5-amino-3-oxo-4-(substituted-phenyl)-2,3-dihydrofurans CHEVRON RESEARCH COMPANY (US) 1986-08-19 US disclosed
EP-0053408-B1 PROCESS FOR THE PREPARATION OF SUBSTITUTED GLYOXYLIC ACID DERIVATIVES STAMICARBON B.V. (NL) 1984-10-17 EP disclosed
US-4417053-A Process for the preparation of substituted glyoxylic acid derivatives STAMICARBON B.V. (NL) 1983-11-22 US disclosed
EP-0053408-A1 Process for the preparation of substituted glyoxylic acid derivatives STAMICARBON B.V. (NL) 1982-06-09 EP disclosed
US-4204044-A SELECTIVE ASYMMETRIC, ENZYMATIC DEHYDROGENATIKN USING STREPTOMYCES, PSEUDOMONAS, BACILLUS OR CORYNEFORM MICROORGANISMS HOFFMANN-LA ROCHE INC. (US) 1980-05-20 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 (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-20230055923-A1 ACTIVATING PYRUVATE KINASE R PDK1, PDK2, PKLR SMN1; SMN2 1423/4885LMNA 2040/4885MAPK1 762/4885
US-20240182465-A1 FUSED RING SUBSTITUTED SIX-MEMBERED HETEROCYCLIC COMPOUND, PREPARATION METHOD THEREFOR AND USE THEREOF WEE1, WEE2, HASPIN SMN1; SMN2 4568/4885LMNA 1934/4885MAPK1 300/4885
US-12122778-B2 Activating pyruvate kinase R PDK1, PDK2, PKLR SMN1; SMN2 1423/4885LMNA 2040/4885MAPK1 762/4885

“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.