SCHEMBL5013531

SCHEMBL5013531

COc1ccc(CN)cn1.CS(=O)(=O)O

nearest known ligand 0.46

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NNMT P40261 1/20 0.46
NAMPT P43490 1/20 0.45
KLKB1 P03952 1/20 0.44
LOXL2 Q9Y4K0 2/20 0.44
LOX P28300 1/20 0.44
TAS2R14 Q9NYV8 1/20 0.43
KMT2A Q03164 3/20 0.43
MAPT P10636 3/20 0.43
MEN1 O00255 2/20 0.43
KDM4E B2RXH2 1/20 0.43
KCNH2 Q12809 1/20 0.43
NPC1 O15118 3/20 0.42
LMNA P02545 3/20 0.42
PKM P14618 1/20 0.42
MKNK1 Q9BUB5 1/20 0.42
MKNK2 Q9HBH9 1/20 0.42
S1PR2 O95136 2/20 0.42
S1PR4 O95977 2/20 0.42
ALDH1A1 P00352 2/20 0.42
S1PR1 P21453 2/20 0.42

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
SCHEMBL29658888 0.88 LOXL2 (0.53) NNMTKLKB1LOXL2LOXKMT2A
SCHEMBL1146238 0.88 LOXL2 (0.53) NNMTKLKB1LOXL2LOXKMT2A
SCHEMBL5547238 0.88 LOXL2 (0.53) NNMTKLKB1LOXL2LOXKMT2A
Hydrochloric Acid SCHEMBL5013392 0.86 LOXL2 (0.52) NNMTKLKB1LOXL2LOXKMT2A
Ammonia Solution, Strong SCHEMBL6061986 0.86 LOXL2 (0.52) NNMTKLKB1LOXL2LOXTAS2R14
Hydrochloric Acid SCHEMBL6234391 0.86 LOXL2 (0.52) NNMTKLKB1LOXL2LOXKMT2A
SCHEMBL5013529 0.77 NAMPT (0.48) NAMPTTAS2R14KMT2AMAPTMEN1
SCHEMBL5008269 0.77 ALDH1A1 (0.49) NAMPTKMT2AMAPTMEN1KDM4E
SCHEMBL5013443 0.77 ALDH1A1 (0.49) NAMPTKMT2AMAPTMEN1KDM4E
SCHEMBL28597113 0.76 TAS2R14 (0.44) NNMTNAMPTTAS2R14KMT2AMAPT

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-1884513-A1 PYRAZOLE COMPOUND AND THERAPEUTIC AGENT FOR DIABETES COMPRISING THE SAME Japan Tobacco, Inc. (JP) 2008-02-06 EP claimed
US-20070032529-A1 Pyrazole compounds and their use as antidiabetes agents JAPAN TOBACCO INC. (JP) 2007-02-08 US claimed
EP-1884513-A1 PYRAZOLE COMPOUND AND THERAPEUTIC AGENT FOR DIABETES COMPRISING THE SAME Japan Tobacco, Inc. (JP) 2008-02-06 EP disclosed
US-20070032529-A1 Pyrazole compounds and their use as antidiabetes agents JAPAN TOBACCO INC. (JP) 2007-02-08 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-20070032529-A1 Pyrazole compounds and their use as antidiabetes agents PYGL, GYS2, AGL NNMT 2977/4885NAMPT 2652/4885KLKB1 3656/4885

“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.