SCHEMBL11943264

SCHEMBL11943264

CCN(CC)CCNc1c(N2CCN(C(=O)Nc3ccc(C(F)(F)F)cc3)CC2)cnn(-c2ccccc2)c1=O

nearest known ligand 0.49

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
▸ TRPV1 Q8NER1 7/20 0.49
▸ MAPT P10636 5/20 0.46
▸ LMNA P02545 4/20 0.45
▸ SMN1; SMN2 Q16637 3/20 0.45
▸ HTT P42858 2/20 0.45
▸ KMT2A Q03164 1/20 0.44
▸ NPSR1 Q6W5P4 1/20 0.44
▸ FAAH O00519 1/20 0.42
▸ GOT1 P17174 1/20 0.42
▸ DCTPP1 Q9H773 1/20 0.42
▸ PDGFRB P09619 1/20 0.41
▸ GAA P10253 1/20 0.41
▸ HSD17B10 Q99714 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
SCHEMBL11946582 0.89 TRPV1 (0.49) TRPV1MAPTLMNASMN1; SMN2HTT
SCHEMBL11943153 0.87 TRPV1 (0.50) TRPV1MAPTLMNASMN1; SMN2HTT
SCHEMBL16300919 0.86 TRPV1 (0.51) TRPV1MAPTLMNASMN1; SMN2HTT
SCHEMBL11943157 0.84 TRPV1 (0.53) TRPV1MAPTLMNASMN1; SMN2HTT
SCHEMBL11943161 0.82 TRPV1 (0.47) TRPV1MAPTLMNASMN1; SMN2HTT
SCHEMBL13328841 0.77 MAPT (0.41) MAPTLMNASMN1; SMN2HTTKMT2A
SCHEMBL11943147 0.76 POLB (0.43) MAPTLMNASMN1; SMN2KMT2ADCTPP1
SCHEMBL11943298 0.76 SMN1; SMN2 (0.43) MAPTLMNASMN1; SMN2HTTKMT2A
SCHEMBL11943165 0.74 PANK3 (0.47) TRPV1MAPTSMN1; SMN2KMT2AFAAH
SCHEMBL11943219 0.73 ALDH1A1 (0.39) MAPTLMNASMN1; SMN2HTTKMT2A

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 TRPV1 4730/4885MAPT 2295/4885LMNA 929/4885
US-20100158992-A1 PIPERAZINE-SUBSTITUTED PYRIDAZINONE DERIVATIVES USEFUL AS GLUCAN SYNTHASE INHIBITORS DPM1, GMPS, MAN2A1 TRPV1 4764/4885MAPT 3651/4885LMNA 1760/4885

“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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