SCHEMBL11899516

SCHEMBL11899516

COC(=O)c1cc(SC)cn1Cc1cc(Cl)ccc1[N+](=O)[O-]

nearest known ligand 0.44

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
▸ MEN1 O00255 4/20 0.44
▸ KMT2A Q03164 4/20 0.44
▸ TRPV1 Q8NER1 1/20 0.41
▸ TDP1 Q9NUW8 1/20 0.41
▸ SMN1; SMN2 Q16637 1/20 0.38
▸ MAPT P10636 6/20 0.37
▸ ALDH1A1 P00352 3/20 0.37
▸ POLB P06746 2/20 0.37
▸ NOS3 P29474 1/20 0.37
▸ NOS1 P29475 1/20 0.37
▸ NOS2 P35228 1/20 0.37
▸ PLA2G1B P04054 1/20 0.37
▸ ATG4B Q9Y4P1 1/20 0.37
▸ MAPK1 P28482 2/20 0.36
▸ PKM P14618 1/20 0.36
▸ HTT P42858 1/20 0.36
▸ KDM4E B2RXH2 1/20 0.36
▸ L3MBTL1 Q9Y468 1/20 0.36

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
SCHEMBL11898666 0.88 MAPT (0.38) MEN1KMT2ATDP1SMN1; SMN2MAPT
SCHEMBL11898992 0.88 KMT2A (0.48) MEN1KMT2ATDP1SMN1; SMN2MAPT
SCHEMBL11914098 0.86 MEN1 (0.46) MEN1KMT2ATDP1SMN1; SMN2MAPT
SCHEMBL11899524 0.85 KMT2A (0.46) MEN1KMT2ATDP1SMN1; SMN2MAPT
SCHEMBL11899080 0.83 ABL1 (0.45) MEN1KMT2ASMN1; SMN2MAPTALDH1A1
SCHEMBL11899083 0.82 KMT2A (0.43) MEN1KMT2ATDP1SMN1; SMN2MAPT
SCHEMBL11898964 0.77 KMT2A (0.49) MEN1KMT2ATDP1SMN1; SMN2MAPT
SCHEMBL11914099 0.76 MAPT (0.41) MEN1KMT2ATDP1SMN1; SMN2MAPT
SCHEMBL11899094 0.75 KMT2A (0.48) MEN1KMT2ATDP1SMN1; SMN2MAPT
SCHEMBL11898601 0.73 MAPT (0.39) MEN1KMT2ATDP1SMN1; SMN2MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2683719-B1 SUBSTITUTED [(5H-PYRROLO[2,1-c] [1,4]BENZODIAZEPIN-11-YL)PIPERAZIN-1-YL]-2,2-DIMETHYLPROPANOIC ACID COMPOUNDS AS DUAL ACTIVITY H1 INVERSE AGONISTS/5-HT2A ANTAGONISTS LILLY CO ELI (US) 2015-03-18 — — EP disclosed
US-8314092-B2 Substituted [(5H-pyrrolo[2,1-c][1,4]benzodiazepin-11-yl)piperazin-1-yl]-2,2-dimethylpropanoic acid compounds as dual activity H1 inverse agonists/5-HT2A antagonists ELI LILLY AND COMPANY (US) 2012-11-20 — — US disclosed
WO-2012109011-A1 SUBSTITUTED [(5H-PYRROLO[2,1-c] [1,4]BENZODIAZEPIN-11-YL)PIPERAZIN-1-YL]-2,2-DIMETHYLPROPANOIC ACID COMPOUNDS AS DUAL ACTIVITY H1 INVERSE AGONISTS/5-HT2A ANTAGONISTS ELI LILLY AND COMPANY (US) 2012-08-16 — — WO disclosed
US-20120202797-A1 SUBSTITUTED [(5H-PYRROLO[2,1-c][1,4]BENZODIAZEPIN-11-YL)PIPERAZIN-1-YL]-2,2-DIMETHYLPROPANOIC ACID COMPOUNDS AS DUAL ACTIVITY H1 INVERSE AGONISTS/5-HT2A ANTAGONISTS ELI LILLY AND COMPANY (US) 2012-08-09 — — 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 (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-20120202797-A1 SUBSTITUTED [(5H-PYRROLO[2,1-c][1,4]BENZODIAZEPIN-11-YL)PIPERAZIN-1-YL]-2,2-DIMETHYLPROPANOIC ACID COMPOUNDS AS DUAL ACTIVITY H1 INVERSE AGONISTS/5-HT2A ANTAGONISTS HTR2A, HTR1A, HTR2C MEN1 1930/4885KMT2A 245/4885TRPV1 147/4885

“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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