SCHEMBL3971733

SCHEMBL3971733

CON=Cc1ccc(F)cc1

nearest known ligand 0.52

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
SRC P12931 1/20 0.52
PLA2G7 Q13093 1/20 0.47
NFE2L2 Q16236 3/20 0.47
NPC1 O15118 3/20 0.45
RAB9A P51151 3/20 0.45
GRIN2D O15399 2/20 0.44
GRIN3B O60391 2/20 0.44
GRIN1 Q05586 2/20 0.44
GRIN2A Q12879 2/20 0.44
GRIN2B Q13224 2/20 0.44
GRIN2C Q14957 2/20 0.44
GRIN3A Q8TCU5 2/20 0.44
TRPA1 O75762 2/20 0.42
NQO2 P16083 1/20 0.42
KDM4E B2RXH2 1/20 0.41
CYP1A2 P05177 1/20 0.41
SMN1; SMN2 Q16637 2/20 0.40
GAA P10253 1/20 0.40

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
SCHEMBL3971732 1.00 SRC (0.52) SRCPLA2G7NFE2L2NPC1RAB9A
SCHEMBL13398097 1.00 SRC (0.52) SRCPLA2G7NFE2L2NPC1RAB9A
SCHEMBL13397720 0.88 SRC (0.61) SRCNPC1RAB9AGRIN2DGRIN3B
SCHEMBL3357693 0.79 NPC1 (0.58) SRCNPC1RAB9AGRIN2DGRIN3B
SCHEMBL6871468 0.79 NPC1 (0.58) SRCNPC1RAB9AGRIN2DGRIN3B
SCHEMBL6077468 0.77 GRIN2D (0.53) SRCRAB9AGRIN2DGRIN3BGRIN1
SCHEMBL5105871 0.77 SRC (0.52) SRCNPC1RAB9ASMN1; SMN2GAA
SCHEMBL12756974 0.77 MAOB (0.52) SRCGRIN2DGRIN3BGRIN1GRIN2A
SCHEMBL13128152 0.77 SRC (0.47) SRCNFE2L2NPC1RAB9ACYP1A2
SCHEMBL9841035 0.77 SRC (0.52) SRCNQO2GAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20130012546-A1 FUNGICIDE HYDROXIMOYL-TETRAZOLE DERIVATIVES BAYER CROPSCIENCE AG (DE) 2013-01-10 US disclosed
US-7507838-B2 Process for the preparation of Z-5-carboxymethylene-1,3-dioxolan-4-ones BRISTOL-MYERS SQUIBB COMPANY (US) 2009-03-24 US disclosed
EP-1784395-A1 PROCESS FOR THE PREPARATION OF Z-5-CARBOXYMETHYLENE-1,3-DIOXOLAN-4-ONES Bristol-Myers Squibb Company (US) 2007-05-16 EP disclosed
US-7109186-B2 4-hydroxy-5-oxo-1-(2-[4-methylpiperazin-1-yl]ethyl)-2,5-dihydro-1H-pyrrole-3-carboxylic acid (3,4-dichlorobenzyl)-methyl-amide for human immunodeficiency virus (HIV) treatment BRISTOL-MYERS SQUIBB COMPANY (US) 2006-09-19 US disclosed
WO-2006028733-A1 PROCESS FOR THE PREPARATION OF Z-5-CARBOXYMETHYLENE-1,3-DIOXOLAN-4-ONES BRISTOL-MYERS SQUIBB COMPANY (US) 2006-03-16 WO disclosed
US-20060047129-A1 Process for the preparation of Z-5-carboxymethylene-1,3-dioxolan-4-ones BRISTOL-MYERS SQUIBB COMPANY 2006-03-02 US disclosed
CN-1617849-A HIV integrase inhibitors BRISTOL MYERS SQUIBB CO (US) 2005-05-18 CN disclosed
US-6890942-B2 Acyl sulfonamides as inhibitors of HIV integrase BRISTOL-MYERS SQUIBB COMPANY (US) 2005-05-10 US disclosed
US-20050004232-A1 Acyl sulfonamides as inhibitors of HIV integrase BRISTOL-MYERS SQUIBB COMPANY 2005-01-06 US disclosed
WO-2004103278-A2 ACYL SULFONAMIDES AS INHIBITORS OF HIV INTEGRASE BRISTOL-MYERS SQUIBB COMPANY (US) 2004-12-02 WO disclosed
EP-1467695-A2 HIV INTEGRASE INHIBITORS Bristol-Myers Squibb Company (US) 2004-10-20 EP disclosed
US-6777440-B2 HIV integrase inhibitors BRISTOL-MYERS SQUIBB COMPANY 2004-08-17 US disclosed
US-20040110804-A1 HIV integrase inhibitors BRISTOL-MYERS SQUIBB COMPANY 2004-06-10 US disclosed
WO-2004004657-A2 HIV INTEGRASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2004-01-15 WO disclosed
US-20030176495-A1 HIV Integrase inhibitors BRISTOL-MYERS SQUIBB COMPANY 2003-09-18 US disclosed
WO-2003049690-A2 HIV INTEGRASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2003-06-19 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 (5 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-20050004232-A1 Acyl sulfonamides as inhibitors of HIV integrase ACSS2, ARSA, ASS1 SRC 1175/4885PLA2G7 868/4885NFE2L2 4284/4885
US-20040110804-A1 HIV integrase inhibitors CDKN1A, SAMHD1, CTCF SRC 1543/4885PLA2G7 1180/4885NFE2L2 3546/4885
US-20030176495-A1 HIV Integrase inhibitors MAPT, RIF1, HPRT1 SRC 248/4885PLA2G7 4373/4885NFE2L2 4258/4885
US-20060047129-A1 Process for the preparation of Z-5-carboxymethylene-1,3-dioxolan-4-ones TKT, KTN1, TET1 SRC 2221/4885PLA2G7 3804/4885NFE2L2 4680/4885
US-20130012546-A1 FUNGICIDE HYDROXIMOYL-TETRAZOLE DERIVATIVES HPD, HAAO, CYP8B1 SRC 1841/4885PLA2G7 4105/4885NFE2L2 3528/4885

“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.