SCHEMBL909196

SCHEMBL909196

O=C(O)Cc1cnc2ccccn12

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GGPS1 O95749 1/20 0.55
FDPS P14324 1/20 0.55
GPR84 Q9NQS5 1/20 0.51
ERCC5 P28715 1/20 0.46
NPC1 O15118 2/20 0.46
RAB9A P51151 2/20 0.46
NPSR1 Q6W5P4 2/20 0.45
KDM4E B2RXH2 1/20 0.45
ALDH1A1 P00352 1/20 0.45
GLA P06280 1/20 0.45
GAA P10253 1/20 0.45
HPGD P15428 1/20 0.45
SMN1; SMN2 Q16637 1/20 0.45
HDAC1 Q13547 1/20 0.44
DRD4 P21917 1/20 0.43
DRD3 P35462 1/20 0.43
HDAC4 P56524 1/20 0.43
EPHB3 P54753 1/20 0.43
ADORA2A P29274 1/20 0.42
ADORA3 P0DMS8 1/20 0.42

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 SCHEMBL9121777 0.98 GGPS1 (0.54) GGPS1FDPSGPR84ERCC5NPC1
Hydrochloric Acid SCHEMBL8661446 0.98 GGPS1 (0.54) GGPS1FDPSGPR84ERCC5NPC1
Beta-Alanine SCHEMBL4783165 0.91 GGPS1 (0.48) GGPS1FDPSGPR84ERCC5NPC1
SCHEMBL633944 0.85 GGPS1 (0.57) GGPS1FDPSGPR84ERCC5NPC1
SCHEMBL17519485 0.85 GGPS1 (0.54) GGPS1FDPSGPR84ERCC5NPC1
SCHEMBL3686302 0.85 GGPS1 (0.54) GGPS1FDPSGPR84ERCC5NPC1
SCHEMBL28284831 0.84 GGPS1 (0.52) GGPS1FDPSGPR84ERCC5NPC1
SCHEMBL7961082 0.84 GGPS1 (0.52) GGPS1FDPSGPR84ERCC5NPC1
SCHEMBL21076445 0.82 GGPS1 (0.48) GGPS1FDPSGPR84NPC1RAB9A
SCHEMBL1761303 0.81 GGPS1 (0.53) GGPS1FDPSGPR84ERCC5NPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111057052-B Method for preparing minodronic acid intermediate 2- (imidazo [1, 2-alpha ] pyridine-3-yl) acetate compound 复旦大学 2023-08-22 CN claimed
CN-112390794-B Preparation method of minodronic acid key intermediate 鲁南制药集团股份有限公司 2023-05-26 CN claimed
CN-111057052-A Method for preparing minodronic acid intermediate 2- (imidazo [1,2- α ] pyridine-3-yl) acetic ester compound 复旦大学 2020-04-24 CN claimed
CN-105837635-B A kind of preparation method for being used to treat the minodronic acid of osteoporosis 邱善晓 2017-12-08 CN claimed
CN-106831873-A A kind of technique for preparing high-purity minodronic acid 成都归合科技有限公司 2017-06-13 CN claimed
CN-104945436-B Minodronic acid preparing method 山东罗欣药业集团股份有限公司 2017-02-08 CN claimed
CN-105837635-A Preparation method of minodronic acid for treating osteoporosis 青岛辰达生物科技有限公司 2016-08-10 CN claimed
WO-2016024287-A1 AN IMPROVED PROCESS FOR PREPARING PURE MINODRONIC ACID AND INTERMEDIATES THEREOF IND-SWIFT LABORATORIES LIMITED (IN) 2016-02-18 WO claimed
CN-105111238-A Method for producing minodronic acid monohydrate by using water as solvent ZHONGSHAN HAIHONG MEDICINE CO LTD 2015-12-02 CN claimed
CN-104945436-A Minodronic acid preparing method SHANDONG LUOXIN PHARMACEUTICAL GROUP CO LTD 2015-09-30 CN claimed
US-20090198062-A1 NOVEL PROCESS GENERICS [UK] LIMITED (INCORPORATED IN THE UNITED KINGDOM) (GB) 2009-08-06 US claimed
EP-2041148-A1 NOVEL PROCESS FOR THE PREPARATION OF BISPHOSPHONIC ACIDS Generics Ýuk¨Limited (GB) 2009-04-01 EP claimed
EP-1891081-A1 PROCESS FOR PRODUCING BISPHOSPHONIC ACIDS AND FORMS THEREOF Jubilant Organosys Limited (IN) 2008-02-27 EP claimed
WO-2008004000-A1 NOVEL PROCESS FOR THE PREPARATION OF BISPHOSPHONIC ACIDS GENERICS [UK] LIMITED (GB) 2008-01-10 WO claimed
WO-2006134603-A1 PROCESS FOR PRODUCING BISPHOSPHONIC ACIDS AND FORMS THEREOF JUBILANT ORGANOSYS LIMITED (IN) 2006-12-21 WO claimed
US-20060128960-A1 Novel process for making bisphosphonic acids using diluents other than halogenated hydrocarbons LIDOR-HADAS RAMI 2006-06-15 US claimed
US-7038083-B2 Process for making bisphosphonic acids using diluents other than halogenated hydrocarbons TEVA PHARMACEUTICAL INDUSTRIES, LTD. (IL) 2006-05-02 US claimed
EP-1476451-A1 USE OF CERTAIN DILUENTS FOR MAKING BISPHOSPHONIC ACIDS TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2004-11-17 EP claimed
US-20040043967-A1 Novel process for making bisphosphonic acids using diluents other than halogenated hydrocarbons TEVA PHARMACEUTICALS USA, INC. 2004-03-04 US claimed
WO-2003097655-A1 USE OF CERTAIN DILUENTS FOR MAKING BISPHOSPHONIC ACIDS TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2003-11-27 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 (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-20090198062-A1 NOVEL PROCESS SLC34A3, HPD, SLC10A6 GGPS1 100/4885FDPS 6/4885GPR84 1871/4885

“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.