SCHEMBL5710556

SCHEMBL5710556

CCc1c(C(=O)C(N)=O)c2c(OCC(=O)N(C)OC)cccc2n1Cc1ccccc1

nearest known ligand 0.78

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
PLA2G2A P14555 18/20 0.78
PLA2G10 O15496 7/20 0.78
PLA2G1B P04054 6/20 0.78
PLA2G2E Q9NZK7 6/20 0.78
PLA2G5 P39877 5/20 0.78
PLA2G2F Q9BZM2 4/20 0.78
PLA2G2D Q9UNK4 4/20 0.78
PLA2G6 O60733 1/20 0.78
PLA2G2C Q5R387 1/20 0.78
PLA2G12B Q9BX93 1/20 0.78
PLA2G12A Q9BZM1 1/20 0.78
PLA2G3 Q9NZ20 1/20 0.78

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
SCHEMBL5710672 0.92 PLA2G2A (0.76) PLA2G2APLA2G10PLA2G1BPLA2G2EPLA2G5
SCHEMBL5710595 0.92 PLA2G2A (0.82) PLA2G2APLA2G10PLA2G1BPLA2G2EPLA2G5
SCHEMBL5710622 0.91 PLA2G2A (0.75) PLA2G2APLA2G10PLA2G1BPLA2G2EPLA2G5
Varespladib SCHEMBL26726 0.88 PLA2G2A (1.00) PLA2G2APLA2G10PLA2G1BPLA2G2EPLA2G5
Varespladib SCHEMBL29358982 0.88 PLA2G2A (1.00) PLA2G2APLA2G10PLA2G1BPLA2G2EPLA2G5
SCHEMBL5710585 0.87 PLA2G2A (0.78) PLA2G2APLA2G10PLA2G1BPLA2G2EPLA2G5
Varespladib Methyl SCHEMBL29378302 0.87 PLA2G2A (0.83) PLA2G2APLA2G10PLA2G1BPLA2G2EPLA2G5
Varespladib Methyl SCHEMBL25678 0.87 PLA2G2A (0.83) PLA2G2APLA2G10PLA2G1BPLA2G2EPLA2G5
SCHEMBL5710593 0.86 PLA2G2A (0.76) PLA2G2APLA2G10PLA2G1BPLA2G2EPLA2G5
SCHEMBL5710588 0.86 PLA2G2A (0.76) PLA2G2APLA2G10PLA2G1BPLA2G2EPLA2G5

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 10 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1220839-B1 HYDROXYFUNCTIONAL AMIDE 1H-INDOLE DERIVATIVES ACTIVE AS SPLA2 INHIBITORS LILLY CO ELI (US) 2006-12-06 EP claimed
US-6939890-B2 Antiinflammatory agents; sepsis shock; rheumatic disorders ELI LILLY AND COMPANY (US) 2005-09-06 US claimed
EP-1220839-A2 HYDROXYFUNCTIONAL AMIDE 1H-INDOLE DERIVATIVES ACTIVE AS SPLA2 INHIBITORS ELI LILLY AND COMPANY (US) 2002-07-10 EP claimed
WO-2001021587-A2 HYDROXYFUNCTIONAL AMIDE 1H-INDOLE DERIVATIVES ACTIVE AS SPLA2 INHIBITORS ELI LILLY AND COMPANY (US) 2001-03-29 WO claimed
EP-1220839-B1 HYDROXYFUNCTIONAL AMIDE 1H-INDOLE DERIVATIVES ACTIVE AS SPLA2 INHIBITORS LILLY CO ELI (US) 2006-12-06 EP disclosed
US-6939890-B2 Antiinflammatory agents; sepsis shock; rheumatic disorders ELI LILLY AND COMPANY (US) 2005-09-06 US disclosed
US-6831095-B1 Treatment of rheumatoid arthritis ELI LILLY AND COMPANY 2004-12-14 US disclosed
US-20040029948-A1 Novel sPLA2 inhibitors HARPER RICHARD WALTZ (US) 2004-02-12 US disclosed
EP-1220839-A2 HYDROXYFUNCTIONAL AMIDE 1H-INDOLE DERIVATIVES ACTIVE AS SPLA2 INHIBITORS ELI LILLY AND COMPANY (US) 2002-07-10 EP disclosed
WO-2001021587-A2 HYDROXYFUNCTIONAL AMIDE 1H-INDOLE DERIVATIVES ACTIVE AS SPLA2 INHIBITORS ELI LILLY AND COMPANY (US) 2001-03-29 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 (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-20040029948-A1 Novel sPLA2 inhibitors PLA2G12A, PLA2G4A, PLAAT2 PLA2G2A 17/4885PLA2G10 11/4885PLA2G1B 10/4885

“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.