SCHEMBL956295

SCHEMBL956295

Cc1ccc(S(=O)(=O)O)cc1.Cc1ccc(S(=O)(=O)O)cc1.Cc1nn2ccc(OCCN3CCN(S(C)(=O)=O)CC3)cc2c1-c1nc(-c2ccccc2)c(-c2nc[nH]n2)s1

nearest known ligand 0.38

Known targets — ChEMBL curated mechanism

ABL1BMXBRAFBTKCHRNA4CHRNB2CSNK1EEGFRERBB2F10FLT1FLT3FLT4IGF1RINSRITKJAK3KDRKITOPRM1PARP1PARP2PDGFRBPIK3CDRAF1RETSLC18A2TECTXKdacAdacBdacCftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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
FLT1 known ✓ P17948 1/20 0.30
KDR known ✓ P35968 1/20 0.30
FLT3 known ✓ P36888 1/20 0.30
JAK3 known ✓ P52333 1/20 0.30
ALK Q9UM73 1/20 0.32
KCNA5 P22460 2/20 0.32
ENPP1 P22413 1/20 0.32
ADORA2A P29274 3/20 0.31
ADORA1 P30542 3/20 0.31
HRH3 Q9Y5N1 2/20 0.30
AURKA O14965 1/20 0.30
DRD3 P35462 1/20 0.30
NTRK1 P04629 1/20 0.30
MAPK14 Q16539 1/20 0.30
ADORA3 P0DMS8 1/20 0.30
ADORA2B P29275 1/20 0.30
ESR1 P03372 1/20 0.30
ESR2 Q92731 1/20 0.30
JAK2 O60674 1/20 0.30
PTK2 Q05397 1/20 0.30

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
SCHEMBL953161 0.94 LCK (0.34) KCNA5ENPP1ADORA2AADORA1HRH3
SCHEMBL952131 0.94 ALK (0.35) ALKADORA2AADORA1HRH3KDR
SCHEMBL952583 0.92 KCNA5 (0.36) ALKKCNA5ENPP1KDRDRD3
SCHEMBL955622 0.91 LTA4H (0.34) ENPP1ADORA2AADORA1
SCHEMBL958287 0.91 HTR1A (0.33) KCNA5ENPP1ADORA2AADORA1HRH3
SCHEMBL955494 0.91 ENPP1 (0.31) KCNA5ENPP1ADORA2AADORA1HRH3
SCHEMBL956645 0.89 CHEK1 (0.37) ADORA2AADORA1HRH3FLT3ADORA3
SCHEMBL954073 0.89 ADCY10 (0.32) ENPP1ADORA2AADORA1
SCHEMBL956777 0.86 HRH3 (0.36) ADORA2AADORA1HRH3DRD3
SCHEMBL951975 0.85 SIGMAR1 (0.39) ALKKCNA5HRH3KDRDRD3

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-9139589-B2 Heteroaryls and uses thereof MILLENNIUM PHARMACEUTICALS, INC. (US) 2015-09-22 US disclosed
US-9090601-B2 Thiazole derivatives MILLENNIUM PHARMACEUTICALS, INC. (US) 2015-07-28 US disclosed
EP-2391619-A1 HETEROARYLS AND THEIR USE AS PI3K INHIBITORS Millennium Pharmaceuticals, Inc. (US) 2011-12-07 EP disclosed
US-20110003807-A1 Thiazole derivatives MILLENNIUM PHARMACEUTICALS, INC. (US) 2011-01-06 US disclosed
US-20110003806-A1 Heteroaryls and uses thereof MILLENNIUM PHARMACEUTICALS, INC. (US) 2011-01-06 US disclosed
WO-2010090716-A1 HETEROARYLS AND THEIR USE AS PI3K INHIBITORS MILLENNIUM PHARMACEUTICALS, INC. (US) 2010-08-12 WO 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-20110003807-A1 Thiazole derivatives MTOR, RICTOR, AKT2 FLT1 1492/4885KDR 1800/4885FLT3 493/4885
US-20110003806-A1 Heteroaryls and uses thereof RICTOR, MTOR, AKT1S1 FLT1 237/4885KDR 195/4885FLT3 1469/4885

“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.