SCHEMBL3314857

SCHEMBL3314857

CS(=O)(=O)O.NC(=O)c1ccc(Oc2ccc(F)cc2)cc1

nearest known ligand 0.63

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
MAOB known ✓ P27338 1/20 0.54
F2 known ✓ P00734 1/20 0.49
BCL2L1 known ✓ Q07817 1/20 0.47
MCL1 known ✓ Q07820 1/20 0.47
PARP10 Q53GL7 13/20 0.63
PARP15 Q460N3 4/20 0.63
PARP14 Q460N5 2/20 0.63
PARP4 Q9UKK3 2/20 0.63
ALDH1A1 P00352 1/20 0.63
KMT2A Q03164 1/20 0.63
PARP16 Q8N5Y8 1/20 0.63
PARP11 Q9NR21 1/20 0.63
PARP3 Q9Y6F1 1/20 0.51
PARP2 Q9UGN5 3/20 0.50
SCN9A Q15858 2/20 0.50
SOS1 Q07889 1/20 0.50
TNKS O95271 1/20 0.50
TNKS2 Q9H2K2 1/20 0.50
CA1 P00915 1/20 0.50
CA2 P00918 1/20 0.50

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
SCHEMBL3016749 0.89 PARP10 (0.79) PARP10PARP15PARP14PARP4ALDH1A1
SCHEMBL3314861 0.81 SOS1 (0.55) PARP10ALDH1A1KMT2AMAOBSCN9A
Fumaric Acid SCHEMBL3023454 0.80 PARP10 (0.63) PARP10PARP15PARP14PARP4ALDH1A1
SCHEMBL3137816 0.80 PARP10 (1.00) PARP10PARP15PARP14PARP4ALDH1A1
SCHEMBL3701690 0.80 OPRM1 (0.63) PARP10PARP15PARP14PARP4ALDH1A1
SCHEMBL1448270 0.79 PGR (0.63) PARP10PARP15PARP14PARP4ALDH1A1
SCHEMBL703171 0.79 BCL2L1 (0.59) SCN9ASOS1BCL2L1MCL1
SCHEMBL12441973 0.78 CES2 (0.62) PARP10PARP15PARP14PARP4ALDH1A1
SCHEMBL52708 0.78 CES2 (0.62) PARP10PARP15PARP14PARP4ALDH1A1
SCHEMBL6453037 0.75 PARP10 (0.61) PARP10PARP15PARP14PARP4ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100105651-A1 ANTAGONISTS OF SNS SODIUM CHANNELS VERNALIS (R&D) LIMITED (GB) 2010-04-29 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-20100105651-A1 ANTAGONISTS OF SNS SODIUM CHANNELS CNR1, OPRL1, CHRNA10 MAOB 594/4885F2 3487/4885BCL2L1 2602/4885

“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.