SCHEMBL8679482

SCHEMBL8679482

O=C([O-])c1ccccc1Br.[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 14)

geneUniProtsupporting neighboursconfidence
CA2 known ✓ P00918 2/20 0.46
CA4 known ✓ P22748 1/20 0.46
CA1 known ✓ P00915 1/20 0.43
ALDH1A1 P00352 5/20 0.58
HPGD P15428 4/20 0.58
KDM4E B2RXH2 1/20 0.58
NPC1 O15118 1/20 0.46
RAB9A P51151 1/20 0.46
MEN1 O00255 2/20 0.43
KMT2A Q03164 2/20 0.43
ELANE P08246 1/20 0.43
POLB P06746 1/20 0.42
SMN1; SMN2 Q16637 2/20 0.41
HSD17B10 Q99714 1/20 0.41

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
Zinc Ion SCHEMBL31152542 0.95 ALDH1A1 (0.52) ALDH1A1HPGDKDM4ECA2CA4
SCHEMBL8613576 0.95 ALDH1A1 (0.52) ALDH1A1HPGDKDM4ECA2CA4
SCHEMBL8678737 0.95 ALDH1A1 (0.52) ALDH1A1HPGDKDM4ECA2CA4
SCHEMBL30459298 0.95 ALDH1A1 (0.52) ALDH1A1HPGDKDM4ECA2CA4
Potassium Ion SCHEMBL2112433 0.95 ALDH1A1 (0.52) ALDH1A1HPGDKDM4ECA2CA4
SCHEMBL7983270 0.83 ALDH1A1 (0.45) ALDH1A1HPGDKDM4ECA2CA4
Phthalic Acid SCHEMBL105218 0.82 ALDH1A1 (0.71) ALDH1A1HPGDKDM4ECA2CA4
Phthalic Acid SCHEMBL28409980 0.82 ALDH1A1 (0.71) ALDH1A1HPGDKDM4ECA2CA4
SCHEMBL10631095 0.80 HPGD (0.47) ALDH1A1HPGDKDM4ECA2CA4
Phthalic Acid SCHEMBL32678845 0.79 ALDH1A1 (0.68) ALDH1A1HPGDKDM4ECA2CA4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105934425-B EBNA1 inhibitors and methods of use thereof 威斯塔解剖学和生物学研究所 2020-08-07 CN disclosed
US-10092537-B2 Use for PAI-1 inhibitor RENASCIENCE CO., LTD. (JP) 2018-10-09 US disclosed
US-20160158188-A1 NOVEL USE FOR PAI-1 INHIBITOR RENASCIENCE CO., LTD. (JP) 2016-06-09 US disclosed
WO-1998006688-A1 CATALYSED COUPLING OF ARYL MAGNESIUM HALOGENIDES AND BROMARYL CARBOXYLIC ACID COMPOUNDS FOR PREPARING BIPHENYL CARBOXYLIC ACIDS GREAT LAKES CHEMICAL KONSTANZ GMBH (DE) 1998-02-19 WO disclosed
EP-0307074-B1 ANTIFOULING COATING FOR POLYMERISATION REACTORS Crown Berger Limited (GB) 1993-09-29 EP disclosed
US-4957982-A PROTECTIVE COATED SURFACES CROWN DECORATIVE PRODUCTS LIMITED (GB) 1990-09-18 US disclosed
EP-0307074-A2 Antifouling coating for polymerisation reactors Crown Berger Limited (GB) 1989-03-15 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 (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-20160158188-A1 NOVEL USE FOR PAI-1 INHIBITOR SERPINE1, SERPINC1, SERPINB1 CA2 4852/4885CA4 4739/4885CA1 3817/4885
US-10092537-B2 Use for PAI-1 inhibitor SERPINE1, SERPINC1, SERPINB1 CA2 4842/4885CA4 4729/4885CA1 3658/4885

“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.