SCHEMBL6408412

SCHEMBL6408412

O=C(O)c1cc2ccc(OCCN3CCOCC3)cc2o1

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 1/20 0.65
KDM4E B2RXH2 4/20 0.54
TP53 P04637 1/20 0.54
TSHR P16473 1/20 0.54
ALDH1A1 P00352 3/20 0.53
MAOB P27338 3/20 0.53
LTA4H P09960 1/20 0.51
SMN1; SMN2 Q16637 2/20 0.51
GAA P10253 1/20 0.51
NPC1 O15118 1/20 0.51
RAB9A P51151 1/20 0.51
AURKB Q96GD4 1/20 0.50
CA12 O43570 1/20 0.50
CA1 P00915 1/20 0.50
CA2 P00918 1/20 0.50
CA7 P43166 1/20 0.50
CA9 Q16790 1/20 0.50
DRD2 P14416 1/20 0.49
DRD3 P35462 1/20 0.49
MAOA P21397 1/20 0.49

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
SCHEMBL3056169 0.91 KDM4E (0.54) CYP1A2KDM4ETP53TSHRALDH1A1
Hydrochloric Acid SCHEMBL7533535 0.90 KDM4E (0.53) CYP1A2KDM4ETP53TSHRALDH1A1
SCHEMBL8229194 0.89 MAOB (0.67) CYP1A2KDM4ETSHRMAOBGAA
SCHEMBL1065576 0.88 CYP1A2 (0.74) CYP1A2KDM4ETP53TSHRALDH1A1
SCHEMBL5105731 0.84 CYP1A2 (0.52) CYP1A2KDM4ETP53TSHRALDH1A1
SCHEMBL6421510 0.81 CYP1A2 (0.53) CYP1A2KDM4ETP53TSHRALDH1A1
SCHEMBL443699 0.81 MAOB (0.55) KDM4ETSHRMAOBLTA4HGAA
SCHEMBL6421505 0.81 CYP1A2 (0.53) CYP1A2KDM4ETP53TSHRALDH1A1
SCHEMBL15623105 0.81 KDM4E (0.58) CYP1A2KDM4ETP53TSHRALDH1A1
SCHEMBL443259 0.80 HDAC1 (0.55) CYP1A2KDM4ETSHRALDH1A1SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20050113402-A1 Substituted pyrrolopyridinone derivatives useful as phosphodiesterase inhibitors SUI ZHIHUA (US) 2005-05-26 US disclosed
US-6818646-B2 1,2,3,4-TETRAHYDRO-2-(5-(2-PYRIDINYL)-PYRIMIDIN-2-YL)-3-(2,3 -DIHYDROBENZOFURANYL)-9H-PYRROLO-(3,4-B)QUINOLIN-9-ONE; MALE ERECTILE DYSFUNCTION; SEXUAL DISORDERS SUI ZHIHUA (US) 2004-11-16 US disclosed
EP-1296981-B1 SUBSTITUTED PYRROLOPYRIDINONE DERIVATIVES USEFUL AS PHOSPHODIESTERASE INHIBITORS ORTHO MCNEIL PHARM INC (US) 2004-10-06 EP disclosed
US-20040044021-A1 Substituted pyrrolopyridinone derivatives useful as phosphodiesterase inhibitors SUI ZHIHUA (US) 2004-03-04 US disclosed
US-6635638-B2 Treatment of sexual dysfunction, cardiovascular system disorders ORTHO-MCNEIL PHARMACEUTICAL, INC. 2003-10-21 US disclosed
EP-1296981-A2 SUBSTITUTED PYRROLOPYRIDINONE DERIVATIVES USEFUL AS PHOSPHODIESTERASE INHIBITORS Ortho-McNeil Pharmaceutical, Inc. (US) 2003-04-02 EP disclosed
US-20020010183-A1 Substituted pyrrolopyridinone derivatives useful as phosphodiesterase inhibitors ORTHO-MCNEIL PHARMACEUTICAL, INC. 2002-01-24 US disclosed
WO-2001087882-A2 SUBSTITUTED PYRROLOPYRIDINONE DERIVATIVES USEFUL AS PHOSPHODIESTERASE INHIBITORS ORTHO-MCNEIL PHARMACEUTICAL, INC. (US) 2001-11-22 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 (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-20050113402-A1 Substituted pyrrolopyridinone derivatives useful as phosphodiesterase inhibitors PDE5A, PDE3A, PDE3B CYP1A2 156/4885KDM4E 1469/4885TP53 4763/4885
US-20040044021-A1 Substituted pyrrolopyridinone derivatives useful as phosphodiesterase inhibitors PDE5A, PDE3A, PDE3B CYP1A2 143/4885KDM4E 1486/4885TP53 4827/4885
US-20020010183-A1 Substituted pyrrolopyridinone derivatives useful as phosphodiesterase inhibitors PDE5A, PDE3A, PDE3B CYP1A2 143/4885KDM4E 1486/4885TP53 4827/4885

“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.