SCHEMBL7515941

SCHEMBL7515941

O=S([O-])c1cccc(Br)c1.[Na+]

nearest known ligand 0.39

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
CA1 known ✓ P00915 1/20 0.32
CA2 known ✓ P00918 1/20 0.32
ALDH1A1 P00352 3/20 0.39
MAPK1 P28482 1/20 0.38
NMT1 P30419 1/20 0.38
PARP1 P09874 1/20 0.36
MGLL Q99685 1/20 0.34
TAAR1 Q96RJ0 2/20 0.33
L3MBTL1 Q9Y468 1/20 0.33
HSD17B3 P37058 1/20 0.33
TP53 P04637 1/20 0.32
C1S P09871 1/20 0.32
NPC1 O15118 1/20 0.32
RAB9A P51151 1/20 0.32
HSD11B1 P28845 1/20 0.32
CA5A P35218 1/20 0.32
CA9 Q16790 1/20 0.32
RAPGEF4 Q8WZA2 1/20 0.32
IDO1 P14902 1/20 0.31
AGXT P21549 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
SCHEMBL10774703 0.84 CA12 (0.30) ALDH1A1NMT1CA2CA5ACA9
SCHEMBL21691192 0.76 PARP1 (0.42) ALDH1A1MAPK1PARP1MGLLL3MBTL1
SCHEMBL1584057 0.76 CES2 (0.40) MAPK1PARP1MGLLTAAR1NPC1
SCHEMBL5632523 0.75 CYP2A6 (0.45) ALDH1A1NMT1L3MBTL1NPC1RAB9A
SCHEMBL1584999 0.74 ACHE (0.46) ALDH1A1MAPK1PARP1MGLLTP53
SCHEMBL7514458 0.74 FAAH (0.34) MGLLIDO1
SCHEMBL7515944 0.74 PARP1 (0.41) ALDH1A1MAPK1PARP1MGLLL3MBTL1
SCHEMBL1466276 0.74 TSHR (0.43) ALDH1A1NMT1PARP1MGLL
SCHEMBL3015881 0.72 CYP2A6 (0.42) ALDH1A1MAPK1NMT1CA1CA2
SCHEMBL25149388 0.71 ALDH1A1 (0.39) ALDH1A1MAPK1PARP1MGLLL3MBTL1

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
CN-120192248-A Alkenyl nitrile compound and preparation method thereof 武汉光化学技术研究院 2025-06-24 CN claimed
CN-120192248-A Alkenyl nitrile compound and preparation method thereof 武汉光化学技术研究院 2025-06-24 CN disclosed
CN-116082204-B Beta-sulfinyl alkenyl sulfone compound and preparation method and application thereof 华南师范大学 2024-07-12 CN disclosed
CN-107540586-B Preparation method of difluoromethyl substituted thioaryl sulfonate 中国科学院上海有机化学研究所 2020-03-10 CN disclosed
EP-1231197-A1 Process for producing allyl halide compound SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2002-08-14 EP disclosed
US-20020107422-A1 Process for producing allyl halide compound SUMITOMO CHEMICAL COMPANY LIMITED (JP) 2002-08-08 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-20020107422-A1 Process for producing allyl halide compound ENY2, ZYX, RPS4Y1 CA1 4462/4885CA2 4250/4885ALDH1A1 1133/4885

“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.