SCHEMBL241537

SCHEMBL241537

CCOC(=O)C(C=O)C=O

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.46
LMNA P02545 1/20 0.43
HSD17B10 Q99714 1/20 0.43
ALOX15 P16050 2/20 0.42
MGAM O43451 1/20 0.42
GAA P10253 1/20 0.42
SI P14410 1/20 0.42
MGAM2 Q2M2H8 1/20 0.42
SOAT1 P35610 1/20 0.42
HCAR2 Q8TDS4 1/20 0.39
TRPA1 O75762 1/20 0.39
NPSR1 Q6W5P4 1/20 0.38
GLO1 Q04760 1/20 0.38
MAPT P10636 2/20 0.36
CYP2D6 P10635 1/20 0.36
CYP2C9 P11712 1/20 0.36
CYP2C19 P33261 1/20 0.36
PIN1 Q13526 1/20 0.35
SMN1; SMN2 Q16637 1/20 0.35
KDM4E B2RXH2 1/20 0.34

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
SCHEMBL31324731 0.82
SCHEMBL23375328 0.80 HCAR2 (0.43) ALDH1A1LMNAHSD17B10HCAR2SMN1; SMN2
SCHEMBL27739897 0.80 CYP2C9 (0.35) ALDH1A1LMNAHSD17B10ALOX15MGAM
SCHEMBL10275655 0.79 ALDH1A1 (0.46) ALDH1A1LMNAHSD17B10ALOX15MGAM
SCHEMBL31324755 0.78 ALDH1A1 (0.40) ALDH1A1LMNAHSD17B10ALOX15MGAM
SCHEMBL31324766 0.78 ALDH1A1 (0.40) ALDH1A1LMNAHSD17B10ALOX15MGAM
SCHEMBL16357720 0.78 ALDH1A1 (0.40) ALDH1A1LMNAHSD17B10ALOX15MGAM
SCHEMBL13312880 0.78 ALDH1A1 (0.35) ALDH1A1LMNAHSD17B10ALOX15MGAM
SCHEMBL524836 0.77
SCHEMBL28230301 0.77 ALDH1A1 (0.43) ALDH1A1LMNAHSD17B10ALOX15MGAM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113943334-B A, A 2A Process for preparing adenosine receptor agonists 常州方圆制药有限公司 2024-04-09 CN claimed
CN-117430647-A Preparation method of regadenoson 康普药业股份有限公司 2024-01-23 CN claimed
WO-2024007890-A1 METHOD FOR PREPARING RUXOLITINIB INTERMEDIATE 济宁学院 2024-01-11 WO claimed
CN-115141180-B Preparation method of ruxotinib intermediate 济宁学院 2023-06-20 CN claimed
CN-116023331-A Synthesis method of 3- (difluoromethyl) -1-methyl-1H-pyrazole-4-carboxylic acid 馨仝(上海)生物科技有限公司 2023-04-28 CN claimed
CN-110483602-B Preparation method of regadenoson 常州方圆制药有限公司 2022-05-17 CN claimed
CN-113943334-A A2AAdenosine receptor agonists 常州方圆制药有限公司 2022-01-18 CN claimed
CN-113004208-A Compound for inhibiting xanthine oxidase activity and preparation method and application thereof 沈阳药科大学 2021-06-22 CN claimed
CN-110078747-B Novel thiazole drug molecule for hospital disinfection and preparation method thereof 河南科技大学第一附属医院 2020-04-10 CN claimed
US-20160244474-A1 PROCESS OF MAKING REGADENOSON AND NOVEL POLYMORPH THEREOF APICORE US LLC (US) 2016-08-25 US claimed
US-20110144320-A1 N-PYRAZOLE A2A RECEPTOR AGONISTS GILEAD PALO ALTO, INC. 2011-06-16 US claimed
US-7956179-B2 Process for preparing an A2A-adenosine receptor agonist and its polymorphs GILEAD SCIENCES, INC. (US) 2011-06-07 US claimed
US-20100179313-A1 PROCESS FOR PREPARING AN A2A-ADENOSINE RECEPTOR AGONIST AND ITS POLYMORPHS GILEAD PALO ALTO, INC. 2010-07-15 US claimed
US-7732595-B2 (1-{9-[(4S,2R,3R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-6-aminopurin-2-yl}pyrazol-4-yl)-N-methylcarboxamide; stable under relative humidity stress GILEAD PALO ALTO, INC. (US) 2010-06-08 US claimed
EP-2158208-A1 PROCESS FOR PREPARING AN A2A-ADENOSINE RECEPTOR AGONIST AND ITS POLYMORPHS CV Therapeutics Inc. (US) 2010-03-03 EP claimed
WO-2008143667-A1 PROCESS FOR PREPARING AN A2A-ADENOSINE RECEPTOR AGONIST AND ITS POLYMORPHS CV THERAPEUTICS, INC. (US) 2008-11-27 WO claimed
EP-1989214-A1 PROCESS FOR PREPARING AN A2A-ADENOSINE RECEPTOR AGONIST AND ITS POLYMORPHS CV THERAPEUTICS, INC. (US) 2008-11-12 EP claimed
US-20070265445-A1 (1-{9-[(4S,2R,3R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-6-aminopurin-2-yl}pyrazol-4-yl)-N-methylcarboxamide; stable under relative humidity stress GILEAD SCIENCES, INC. 2007-11-15 US claimed
US-20070225247-A1 (1-{9-[(4S,2R,3R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-6-aminopurin-2-yl}pyrazol-4-yl)-N-methylcarboxamide; stable under relative humidity stress GILEAD SCIENCES, INC. 2007-09-27 US claimed
WO-2007092372-A1 PROCESS FOR PREPARING AN A2A-ADENOSINE RECEPTOR AGONIST AND ITS POLYMORPHS CV THERAPEUTICS, INC. (US) 2007-08-16 WO claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (5 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-20070265445-A1 (1-{9-[(4S,2R,3R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-6-aminopurin-2-yl}pyrazol-4-yl)-N-methylcarboxamide; stable under relative humidity stress ADORA2A, ADORA3, ADORA2B ALDH1A1 763/4885LMNA 2195/4885HSD17B10 4712/4885
US-20110144320-A1 N-PYRAZOLE A2A RECEPTOR AGONISTS ADORA2A, ADORA3, TBXA2R ALDH1A1 1264/4885LMNA 3247/4885HSD17B10 3993/4885
US-20160244474-A1 PROCESS OF MAKING REGADENOSON AND NOVEL POLYMORPH THEREOF ADORA3, ADORA2A, ADA ALDH1A1 968/4885LMNA 1967/4885HSD17B10 2143/4885
US-20100179313-A1 PROCESS FOR PREPARING AN A2A-ADENOSINE RECEPTOR AGONIST AND ITS POLYMORPHS ADORA2A, ADORA3, ADORA2B ALDH1A1 1160/4885LMNA 1780/4885HSD17B10 3772/4885
US-20070225247-A1 (1-{9-[(4S,2R,3R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-6-aminopurin-2-yl}pyrazol-4-yl)-N-methylcarboxamide; stable under relative humidity stress ADORA2A, ADORA3, ADORA2B ALDH1A1 763/4885LMNA 2195/4885HSD17B10 4712/4885

“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.