SCHEMBL433307

SCHEMBL433307

COC(=O)C1=C(C)NC(C)=C(C(=O)OCC(=O)[O-])C1.[Na+]

nearest known ligand 0.58

Known targets — ChEMBL curated mechanism

ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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 15)

geneUniProtsupporting neighboursconfidence
ADORA3 known ✓ P0DMS8 2/20 0.33
KDM4E B2RXH2 5/20 0.58
KMT2A Q03164 2/20 0.58
MAPT P10636 2/20 0.58
MEN1 O00255 1/20 0.58
ALOX15 P16050 1/20 0.58
SMN1; SMN2 Q16637 2/20 0.35
LMNA P02545 3/20 0.35
ALDH1A1 P00352 2/20 0.34
TP53 P04637 1/20 0.34
TSHR P16473 1/20 0.34
GAA P10253 2/20 0.33
RAB9A P51151 1/20 0.33
L3MBTL1 Q9Y468 1/20 0.33
NPSR1 Q6W5P4 1/20 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
SCHEMBL431670 0.89 KDM4E (0.75) KDM4EKMT2AMAPTMEN1ALOX15
SCHEMBL14963235 0.84 KDM4E (0.62) KDM4EKMT2AMAPTMEN1ALOX15
SCHEMBL14963232 0.84 KDM4E (0.62) KDM4EKMT2AMAPTMEN1ALOX15
SCHEMBL433985 0.84 KDM4E (0.62) KDM4EKMT2AMAPTMEN1ALOX15
SCHEMBL30987784 0.82 KDM4E (0.86) KDM4EKMT2AMAPTMEN1ALOX15
SCHEMBL3295915 0.82 KDM4E (0.64) KDM4EKMT2AMAPTMEN1ALOX15
SCHEMBL10482215 0.77 MAPT (0.60) KDM4EKMT2AMAPTMEN1ALOX15
SCHEMBL23998044 0.76 KDM4E (0.73) KDM4EKMT2AMAPTMEN1ALOX15
SCHEMBL3829818 0.76 MAPT (0.58) KDM4EKMT2AMAPTMEN1ALOX15
SCHEMBL28919085 0.75 KDM4E (0.56) KDM4EKMT2AMAPTMEN1ALOX15

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-20130131126-A1 DERIVATIVES OF 1,4-DIHYDROPYRIDINE POSSESSING ANTIVIRAL EFFICACY JSC GRINDEKS (LV) 2013-05-23 US claimed
EP-2593430-A1 DERIVATIVES OF 1,4-DIHYDROPYRIDINE POSSESSING ANTIVIRAL EFFICACY Grindeks (LV) 2013-05-22 EP claimed
WO-2012010276-A1 DERIVATIVES OF 1,4-DIHYDROPYRIDINE POSSESSING ANTIVIRAL EFFICACY GRINDEKS (LV) 2012-01-26 WO claimed
US-20130131126-A1 DERIVATIVES OF 1,4-DIHYDROPYRIDINE POSSESSING ANTIVIRAL EFFICACY JSC GRINDEKS (LV) 2013-05-23 US disclosed
EP-2593430-A1 DERIVATIVES OF 1,4-DIHYDROPYRIDINE POSSESSING ANTIVIRAL EFFICACY Grindeks (LV) 2013-05-22 EP disclosed
WO-2012010276-A1 DERIVATIVES OF 1,4-DIHYDROPYRIDINE POSSESSING ANTIVIRAL EFFICACY GRINDEKS (LV) 2012-01-26 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 (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-20130131126-A1 DERIVATIVES OF 1,4-DIHYDROPYRIDINE POSSESSING ANTIVIRAL EFFICACY IFNAR1, SARS1, MAVS ADORA3 1559/4885KDM4E 43/4885KMT2A 717/4885

“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.