SCHEMBL1959930

SCHEMBL1959930

COc1ccc(C(C#N)=Cc2ccc(N3CCC(OC(=O)CN(C)C)CC3)s2)cc1OC.Cc1ccc(S(=O)(=O)O)cc1

nearest known ligand 0.59

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 19)

geneUniProtsupporting neighboursconfidence
▸ ABCB1 P08183 1/20 0.59
▸ ABCG2 Q9UNQ0 1/20 0.59
▸ PAX8 Q06710 1/20 0.36
▸ PDE4B Q07343 2/20 0.36
▸ POLB P06746 2/20 0.35
▸ SMN1; SMN2 Q16637 4/20 0.34
▸ ALDH1A1 P00352 3/20 0.34
▸ HPGD P15428 2/20 0.34
▸ PKM P14618 1/20 0.34
▸ LMNA P02545 3/20 0.33
▸ MAPT P10636 3/20 0.33
▸ HTT P42858 2/20 0.33
▸ TSHR P16473 1/20 0.33
▸ KDM4E B2RXH2 1/20 0.32
▸ NPSR1 Q6W5P4 1/20 0.32
▸ HCRTR1 O43613 1/20 0.32
▸ HCRTR2 O43614 1/20 0.32
▸ MAPK1 P28482 1/20 0.32
▸ ELANE P08246 1/20 0.32

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
SCHEMBL1959928 1.00 ABCB1 (0.59) ABCB1ABCG2PAX8PDE4BPOLB
SCHEMBL1959468 0.94 ABCB1 (0.58) ABCB1ABCG2PAX8PDE4BPOLB
SCHEMBL1959467 0.94 ABCB1 (0.58) ABCB1ABCG2PAX8PDE4BPOLB
SCHEMBL1958340 0.92 ABCB1 (0.69) ABCB1ABCG2PDE4BPOLBALDH1A1
SCHEMBL1958342 0.92 ABCB1 (0.69) ABCB1ABCG2PDE4BPOLBALDH1A1
Hydrochloric Acid SCHEMBL1961487 0.91 ABCB1 (0.68) ABCB1ABCG2PDE4BPOLBALDH1A1
Hydrochloric Acid SCHEMBL1961488 0.91 ABCB1 (0.68) ABCB1ABCG2PDE4BPOLBALDH1A1
SCHEMBL1960055 0.87 ABCB1 (0.60) ABCB1ABCG2PAX8PDE4BSMN1; SMN2
SCHEMBL29400000 0.86 ABCB1 (0.63) ABCB1ABCG2PDE4BPOLBLMNA
SCHEMBL1956828 0.85 ABCB1 (0.68) ABCB1ABCG2PDE4BPOLBLMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2332905-B1 BCRP/ABCG2 Inhibitor YAKULT HONSHA KK (JP) 2017-03-01 — — EP disclosed
US-8697742-B2 BCRP/ABCG2 inhibitor KABUSHIKI KAISHA YAKULT HONSHA (JP) 2014-04-15 — — US disclosed
EP-2332905-A1 BCRP/ABCG3 Inhibitor Kabushiki Kaisha Yakult Honsha (JP) 2011-06-15 — — EP disclosed
US-20090253656-A1 BCRP/ABCG2 INHIBITOR KABUSHIKI KAISHA YAKULT HONSHA (JP) 2009-10-08 — — US disclosed
EP-1864972-A1 BCRP/ABCG2 INHIBITOR Kabushiki Kaisha Yakult Honsha (JP) 2007-12-12 — — 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-20090253656-A1 BCRP/ABCG2 INHIBITOR ABCC1, ABCB1, BRCA1 ABCB1 2/4885ABCG2 7/4885PAX8 4366/4885

“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.

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