SCHEMBL11943476

SCHEMBL11943476

Cc1ccc(Cl)cc1NC(=O)N1CCN(c2cnn(-c3ccccc3)c(=O)c2OCc2ccccc2)CC1

nearest known ligand 0.47

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
▸ RBP4 P02753 4/20 0.47
▸ DCTPP1 Q9H773 3/20 0.45
▸ MAPK1 P28482 3/20 0.45
▸ ALDH1A1 P00352 3/20 0.45
▸ RXFP1 Q9HBX9 1/20 0.45
▸ MEN1 O00255 1/20 0.45
▸ KMT2A Q03164 1/20 0.45
▸ P2RY12 Q9H244 1/20 0.43
▸ SMN1; SMN2 Q16637 3/20 0.43
▸ MAPT P10636 3/20 0.43
▸ POLB P06746 1/20 0.42
▸ GRM5 P41594 1/20 0.42
▸ LMNA P02545 1/20 0.42
▸ TP53 P04637 1/20 0.42
▸ KDM4E B2RXH2 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
SCHEMBL13329677 0.92 LMNA (0.50) DCTPP1ALDH1A1RXFP1P2RY12SMN1; SMN2
SCHEMBL11943389 0.90 KMT2A (0.49) DCTPP1ALDH1A1RXFP1KMT2AP2RY12
SCHEMBL11943474 0.84 FAAH (0.49) RBP4DCTPP1MAPK1ALDH1A1RXFP1
SCHEMBL11943382 0.83 MAPT (0.56) DCTPP1MAPK1ALDH1A1RXFP1MEN1
SCHEMBL11943473 0.83 ALDH1A1 (0.49) DCTPP1MAPK1ALDH1A1RXFP1MEN1
SCHEMBL11943385 0.81 NPC1 (0.46) DCTPP1MAPK1ALDH1A1RXFP1MEN1
SCHEMBL11943394 0.80 ALDH1A1 (0.51) DCTPP1MAPK1ALDH1A1RXFP1MEN1
SCHEMBL11943383 0.78 ALDH1A1 (0.49) DCTPP1ALDH1A1RXFP1MEN1KMT2A
SCHEMBL11943391 0.77 SMN1; SMN2 (0.47) DCTPP1ALDH1A1RXFP1SMN1; SMN2MAPT
SCHEMBL11943475 0.77 ALDH1A1 (0.44) DCTPP1ALDH1A1RXFP1P2RY12SMN1; 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 6 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8232274-B2 Pyridazinone derivatives useful as glucan synthase inhibitors ALBANY MOLECULAR RESEARCH, INC. (US) 2012-07-31 — — US disclosed
US-8232274-B2 Pyridazinone derivatives useful as glucan synthase inhibitors ALBANY MOLECULAR RESEARCH, INC. (US) 2012-07-31 — — US disclosed
US-20100158992-A1 PIPERAZINE-SUBSTITUTED PYRIDAZINONE DERIVATIVES USEFUL AS GLUCAN SYNTHASE INHIBITORS SCHERING CORPORATION (US) 2010-06-24 — — US disclosed
US-20100158992-A1 PIPERAZINE-SUBSTITUTED PYRIDAZINONE DERIVATIVES USEFUL AS GLUCAN SYNTHASE INHIBITORS SCHERING CORPORATION (US) 2010-06-24 — — US disclosed
US-20090170861-A1 Pyridazinone Derivatives Useful as Glucan Synthase Inhibitors SCHERING CORPORATION AND ALBANY MOLECULAR RESEARCH, INC. 2009-07-02 — — US disclosed
US-20090170861-A1 Pyridazinone Derivatives Useful as Glucan Synthase Inhibitors SCHERING CORPORATION AND ALBANY MOLECULAR RESEARCH, INC. 2009-07-02 — — US 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 (2 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-20090170861-A1 Pyridazinone Derivatives Useful as Glucan Synthase Inhibitors MAN2A1, GYS2, MANBA RBP4 4125/4885DCTPP1 625/4885MAPK1 1289/4885
US-20100158992-A1 PIPERAZINE-SUBSTITUTED PYRIDAZINONE DERIVATIVES USEFUL AS GLUCAN SYNTHASE INHIBITORS DPM1, GMPS, MAN2A1 RBP4 4580/4885DCTPP1 209/4885MAPK1 775/4885

“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.

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