SCHEMBL3452202

SCHEMBL3452202

O=C([O-])c1cccc(CN(Cc2cccs2)c2ccnc(-c3ccc(OCc4ccccc4)cc3)n2)c1.[Na+]

nearest known ligand 0.40

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 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 1/20 0.40
CYP1A2 P05177 1/20 0.40
HPGD P15428 1/20 0.40
CYP2C19 P33261 1/20 0.40
SMN1; SMN2 Q16637 1/20 0.40
RXFP1 Q9HBX9 1/20 0.40
PTGER1 P34995 1/20 0.38
TRPM8 Q7Z2W7 2/20 0.38
NR4A2 P43354 1/20 0.38
MAPT P10636 1/20 0.38
MRGPRX4 Q96LA9 4/20 0.37
MMP2 P08253 2/20 0.37
MMP13 P45452 2/20 0.37
STK17B O94768 1/20 0.37
PPARD Q03181 2/20 0.37
HCAR3 P49019 1/20 0.37
MMP1 P03956 1/20 0.37
MMP9 P14780 1/20 0.37
PPARA Q07869 1/20 0.37
SMPD1 P17405 1/20 0.36

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
SCHEMBL3452582 0.92 MMP13 (0.41) KDM4ECYP1A2HPGDCYP2C19SMN1; SMN2
SCHEMBL13109714 0.92 MRGPRX4 (0.45) KDM4ECYP1A2HPGDCYP2C19SMN1; SMN2
SCHEMBL3452204 0.92 MRGPRX4 (0.45) KDM4ECYP1A2HPGDCYP2C19SMN1; SMN2
SCHEMBL3453185 0.88 TRPM8 (0.41) KDM4ECYP1A2HPGDCYP2C19SMN1; SMN2
SCHEMBL13109717 0.86 ALOX5 (0.48) KDM4ECYP1A2HPGDCYP2C19SMN1; SMN2
SCHEMBL3452584 0.85 ALOX5 (0.47) KDM4ECYP1A2HPGDCYP2C19SMN1; SMN2
SCHEMBL13109711 0.83 CYP1A2 (0.41) KDM4ECYP1A2HPGDCYP2C19SMN1; SMN2
SCHEMBL3453187 0.82 CYP1A2 (0.41) KDM4ECYP1A2HPGDCYP2C19SMN1; SMN2
Hydrochloric Acid SCHEMBL3453153 0.77 MRGPRX4 (0.43) CYP1A2CYP2C19SMN1; SMN2TRPM8MRGPRX4
SCHEMBL3452201 0.75 SMN1; SMN2 (0.39) KDM4ECYP1A2HPGDCYP2C19SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7820704-B2 Substituted heteroaryl derivatives, compositions, and methods of use TRANSTECH PHARMA, INC. (US) 2010-10-26 US disclosed
US-20050261294-A1 Substituted heteroaryl derivatives, compositions, and methods of use VTVX HOLDINGS I LLC 2005-11-24 US 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-20050261294-A1 Substituted heteroaryl derivatives, compositions, and methods of use MC5R, MC3R, MC4R KDM4E 2378/4885CYP1A2 261/4885HPGD 1777/4885

“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.