SCHEMBL1472997

SCHEMBL1472997

On1ccc2ncccc21

nearest known ligand 0.57

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
RPS6KA5 O75582 11/20 0.57
MET P08581 6/20 0.46
RPS6KA4 O75676 2/20 0.45
CDC7 O00311 1/20 0.45
CDK2 P24941 1/20 0.45
SLC22A12 Q96S37 1/20 0.43
RAPGEF4 Q8WZA2 1/20 0.41

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
SCHEMBL13378058 0.76 RPS6KA5 (0.59) RPS6KA5METRPS6KA4CDC7CDK2
SCHEMBL256322 0.74 RPS6KA5 (0.57) RPS6KA5METRPS6KA4CDC7CDK2
SCHEMBL27987760 0.74 RPS6KA5 (0.57) RPS6KA5METRPS6KA4CDC7CDK2
SCHEMBL10197264 0.74 RPS6KA5 (0.57) RPS6KA5METRPS6KA4CDC7CDK2
SCHEMBL3222371 0.74 RPS6KA5 (0.57) RPS6KA5METRPS6KA4CDC7CDK2
SCHEMBL12011230 0.74 RPS6KA5 (0.57) RPS6KA5METRPS6KA4CDC7CDK2
SCHEMBL1446137 0.74 RPS6KA5 (0.57) RPS6KA5METRPS6KA4CDC7CDK2
SCHEMBL29509090 0.74 RPS6KA5 (0.57) RPS6KA5METRPS6KA4CDC7CDK2
SCHEMBL31609660 0.74 RPS6KA5 (0.52) RPS6KA5METRPS6KA4CDC7CDK2
SCHEMBL30241905 0.72 SLC22A12 (0.56) RPS6KA5METRPS6KA4CDC7CDK2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0916669-B1 Processes and intermediates for the preparation of Pyrrolo(3,2-b)pyridine LILLY CO ELI (US) 2003-04-09 EP claimed
CN-1278814-A Pyrrolo [3,2-b] pyridine processes and intermediates LILLY CO ELI (US) 2001-01-03 CN claimed
US-6150525-A Pyrrolo [3,2-b]pyridine processes and intermediates ELI LILLY AND COMPANY (US) 2000-11-21 US claimed
EP-0916669-A2 Processes and intermediates for the preparation of Pyrrolo(3,2-b)pyridine ELI LILLY AND COMPANY (US) 1999-05-19 EP claimed
US-20160207918-A1 SUBSTITUTED AZAINDOLEOXOACETIC PIPERAZINE DERIVATIVES WITH PROTEASE INHIBITORS VIIV HEALTHCARE UK (NO. 4) LIMITED (GB) 2016-07-21 US disclosed
US-20160152615-A1 PRODRUGS OF SUBSTITUTED AZAINDOLEOXOACETIC PIPERAZINE DERIVATIVES VIIV HEALTHCARE UK (NO. 4) LIMITED (GB) 2016-06-02 US disclosed
US-20160075703-A1 SUBSTITUTED AZAINDOLEOXOACETIC PIPERAZINE DERIVATIVES VIIV HEALTHCARE UK (NO. 4) LIMITED (GB) 2016-03-17 US disclosed
US-20150329543-A1 PRODRUGS OF SUBSTITUTED AZAINDOLEOXOACETIC PIPERAZINE DERIVATIVES VIIV HEALTHCARE UK (NO. 4) LIMITED (GB) 2015-11-19 US disclosed
US-20150259342-A1 SUBSTITUTED AZAINDOLEOXOACETIC PIPERAZINE DERIVATIVES VIIV HEALTHCARE UK (NO. 4) LIMITED (GB) 2015-09-17 US disclosed
US-20150087652-A1 PHARMACEUTICAL FORMULATIONS OF SUBSTITUTED AZAINDOLEOXOACETIC PIPERAZINE DERIVATIVES WITH PROTEASE INHIBITORS VIIV HEALTHCARE UK (NO. 4) LIMITED (GB) 2015-03-26 US disclosed
US-20140135342-A1 PHARMACEUTICAL FORMULATIONS OF SUBSTITUTED AZAINDOLEOXOACETIC PIPERAZINE DERIVATIVES WITH PROTEASE INHIBITORS VIIV HEALTHCARE UK (NO. 4) LIMITED (GB) 2014-05-15 US disclosed
EP-1513832-B1 Indole, azaindole and related heterocyclic 4-alkenyl piperidine amides BRISTOL MYERS SQUIBB CO (US) 2014-03-05 EP disclosed
US-20010044538-A1 p38 MAP kinase inhibitors CHENG SOAN (US) 2001-11-22 US disclosed
US-6316464-B1 P38 MAP kinase inhibitors SYNTEX (U.S.A.) LLC 2001-11-13 US disclosed
CN-1279682-A bicyclic kinase inhibitors HOFFMANN LA ROCHE (CH) 2001-01-10 CN disclosed
CN-1278814-A Pyrrolo [3,2-b] pyridine processes and intermediates LILLY CO ELI (US) 2001-01-03 CN disclosed
US-6150525-A Pyrrolo [3,2-b]pyridine processes and intermediates ELI LILLY AND COMPANY (US) 2000-11-21 US disclosed
EP-1025102-A1 BICYCLIC KINASE INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2000-08-09 EP disclosed
EP-0916669-A2 Processes and intermediates for the preparation of Pyrrolo(3,2-b)pyridine ELI LILLY AND COMPANY (US) 1999-05-19 EP disclosed
WO-1999020624-A1 BICYCLIC KINASE INHIBITORS F.HOFFMANN-LA ROCHE AG (CH) 1999-04-29 WO 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 (8 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-20160152615-A1 PRODRUGS OF SUBSTITUTED AZAINDOLEOXOACETIC PIPERAZINE DERIVATIVES ITPA, IMPDH2, IDO1 RPS6KA5 1542/4885MET 4057/4885RPS6KA4 2282/4885
US-20160075703-A1 SUBSTITUTED AZAINDOLEOXOACETIC PIPERAZINE DERIVATIVES ITPA, IDO1, IDO2 RPS6KA5 344/4885MET 4522/4885RPS6KA4 934/4885
US-20150087652-A1 PHARMACEUTICAL FORMULATIONS OF SUBSTITUTED AZAINDOLEOXOACETIC PIPERAZINE DERIVATIVES WITH PROTEASE INHIBITORS PREP, PEPD, DNPEP RPS6KA5 1951/4885MET 4486/4885RPS6KA4 3033/4885
US-20140135342-A1 PHARMACEUTICAL FORMULATIONS OF SUBSTITUTED AZAINDOLEOXOACETIC PIPERAZINE DERIVATIVES WITH PROTEASE INHIBITORS PREP, PEPD, DNPEP RPS6KA5 1951/4885MET 4486/4885RPS6KA4 3033/4885
US-20150329543-A1 PRODRUGS OF SUBSTITUTED AZAINDOLEOXOACETIC PIPERAZINE DERIVATIVES ITPA, IMPDH2, IDO1 RPS6KA5 1542/4885MET 4057/4885RPS6KA4 2282/4885
US-20150259342-A1 SUBSTITUTED AZAINDOLEOXOACETIC PIPERAZINE DERIVATIVES ITPA, IDO1, IDO2 RPS6KA5 344/4885MET 4522/4885RPS6KA4 934/4885
US-20160207918-A1 SUBSTITUTED AZAINDOLEOXOACETIC PIPERAZINE DERIVATIVES WITH PROTEASE INHIBITORS PREP, PEPD, DNPEP RPS6KA5 1165/4885MET 4367/4885RPS6KA4 1959/4885
US-20010044538-A1 p38 MAP kinase inhibitors MAPK1, MAPK8, MAP3K1 RPS6KA5 174/4885MET 2398/4885RPS6KA4 222/4885

“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.