SCHEMBL5659211

SCHEMBL5659211

CS(=O)(=O)O.OCCc1ccccc1-c1ccccc1

nearest known ligand 0.47

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
SLC6A2 known ✓ P23975 3/20 0.41
SLC6A4 known ✓ P31645 2/20 0.41
SLC6A3 known ✓ Q01959 2/20 0.41
KMT2A Q03164 1/20 0.47
PTGS2 P35354 1/20 0.46
DPP4 P27487 1/20 0.46
PTGER3 P43115 3/20 0.45
PTGER1 P34995 2/20 0.45
PTGER4 P35408 2/20 0.45
PTGER2 P43116 2/20 0.45
FOLH1 Q04609 1/20 0.45
PDCD1 Q15116 1/20 0.44
CD274 Q9NZQ7 1/20 0.44
FFAR1 O14842 2/20 0.42
FFAR4 Q5NUL3 2/20 0.42
HDAC3 O15379 1/20 0.42
HDAC1 Q13547 1/20 0.42
HDAC2 Q92769 1/20 0.42
HDAC6 Q9UBN7 1/20 0.42
CA12 O43570 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
SCHEMBL28295855 0.88 PPARA (0.49) KMT2APTGS2DPP4PTGER3PTGER1
SCHEMBL429540 0.87 DPP4 (0.58) KMT2ADPP4PTGER3PTGER1PTGER4
SCHEMBL27840283 0.87 DPP4 (0.58) KMT2ADPP4PTGER3PTGER1PTGER4
SCHEMBL28293956 0.83 PPARA (0.52)
SCHEMBL8604437 0.83 PTGS2 (0.61) PTGS2
SCHEMBL10609360 0.81 DPP4 (0.50) KMT2ADPP4PTGER3PTGER1PTGER4
SCHEMBL27615436 0.80 PTGS2 (0.65) KMT2APTGS2HDAC2HDAC6CA12
SCHEMBL5584302 0.80 TAAR1 (0.52) SLC6A2SLC6A4SLC6A3
SCHEMBL6075489 0.78 TAAR1 (0.48) KMT2ACA12CA1CA2CA7
Sulfuric Acid SCHEMBL9303438 0.77 PPARA (0.52)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7166617-B2 Cyclic amide derivatives MITSUBISHI PHARMA CORPORATION (JP) 2007-01-23 US disclosed
US-20030212094-A1 Novel cyclic amide derivatives MITSUBISHI PHARMA CORPORATION (JP) 2003-11-13 US disclosed
EP-1260512-A1 NOVEL CYCLIC AMIDE DERIVATIVES Mitsubishi Pharma Corporation (JP) 2002-11-27 EP 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-20030212094-A1 Novel cyclic amide derivatives SIGMAR1, OPRM1, OPRD1 SLC6A2 1499/4885SLC6A4 965/4885SLC6A3 1601/4885

“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.