SCHEMBL951946

SCHEMBL951946

Cc1ccc(S(=O)(=O)O)cc1.Cc1ccc(S(=O)(=O)O)cc1.Cc1nn2ccc(OCCN3CCOCC3)cc2c1-c1nc(-c2ccccc2F)c(-c2nc[nH]n2)s1

nearest known ligand 0.35

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
JAK3 known ✓ P52333 1/20 0.35
FLT3 known ✓ P36888 2/20 0.33
JAK2 O60674 1/20 0.35
PTK2 Q05397 1/20 0.35
ADORA2A P29274 2/20 0.33
ADORA1 P30542 2/20 0.33
ADORA3 P0DMS8 1/20 0.33
ADORA2B P29275 1/20 0.33
CNR1 P21554 2/20 0.33
CNR2 P34972 2/20 0.33
MAPK14 Q16539 3/20 0.32
GPR55 Q9Y2T6 1/20 0.32
CA12 O43570 1/20 0.32
CA1 P00915 1/20 0.32
CA2 P00918 1/20 0.32
CA7 P43166 1/20 0.32
CA9 Q16790 1/20 0.32
PDE2A O00408 1/20 0.32
ALOX5 P09917 1/20 0.32
NFE2L2 Q16236 2/20 0.31

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
SCHEMBL953795 0.94 ENPP1 (0.35) JAK2JAK3PTK2ADORA2AADORA1
SCHEMBL954160 0.93 PDE2A (0.36) JAK2JAK3PTK2ADORA2AADORA1
SCHEMBL956645 0.89 CHEK1 (0.37) ADORA2AADORA1FLT3ADORA3ADORA2B
SCHEMBL958287 0.86 HTR1A (0.33) ADORA2AADORA1ADORA3ADORA2BKDM4E
SCHEMBL952318 0.86 HRH3 (0.36) ADORA2AADORA1PDE2ANPC1RAB9A
SCHEMBL953161 0.85 LCK (0.34) ADORA2AADORA1FLT3ADORA3ADORA2B
SCHEMBL6845055 0.84 CNR1 (0.37) ADORA2AADORA1CNR1CNR2MAPK14
SCHEMBL955494 0.84 ENPP1 (0.31) ADORA2AADORA1
SCHEMBL956295 0.84 ALK (0.32) JAK2JAK3PTK2ADORA2AADORA1
SCHEMBL6842775 0.83 SYK (0.34) CNR1CNR2MAPK14GPR55PDE2A

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 JAK3 118/4885FLT3 493/4885JAK2 14/4885
US-20110003806-A1 Heteroaryls and uses thereof RICTOR, MTOR, AKT1S1 JAK3 264/4885FLT3 1469/4885JAK2 44/4885

“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.