SCHEMBL9492990

SCHEMBL9492990

CCCCCCCCCCCCC(C(=O)[O-])C(O)(CC(=O)[O-])C(=O)[O-].CCCCCCCCCCCCC(C(=O)[O-])C(O)(CC(=O)[O-])C(=O)[O-].[Ca+2].[Ca+2].[Ca+2]

nearest known ligand 0.51

Known targets — ChEMBL curated mechanism

GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHMGCRMMP1MMP13MMP7MMP8PTGS1PTGS2ileSpolrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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
HSPD1 P10809 1/20 0.51
BLM P54132 1/20 0.51
HSPE1 P61604 1/20 0.51
CA2 P00918 1/20 0.45
MEN1 O00255 1/20 0.43
HPGD P15428 1/20 0.43
RECQL P46063 1/20 0.43
KMT2A Q03164 1/20 0.43
HSD17B10 Q99714 1/20 0.43
CA1 P00915 2/20 0.43
USP2 O75604 1/20 0.43
LMNA P02545 1/20 0.43
GPR84 Q9NQS5 5/20 0.41
NFKB1 P19838 1/20 0.39
CES2 O00748 1/20 0.38

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 SCHEMBL9496396 0.97 HSPD1 (0.51) HSPD1BLMHSPE1CA2MEN1
SCHEMBL31158245 0.97 HSPD1 (0.51) HSPD1BLMHSPE1CA2MEN1
Potassium Ion SCHEMBL31158247 0.97 HSPD1 (0.51) HSPD1BLMHSPE1CA2MEN1
Tetramethylammonium Ion SCHEMBL31158235 0.94 HSPD1 (0.49) HSPD1BLMHSPE1CA2MEN1
Tetrabuthylammonium SCHEMBL31158248 0.91 HSPD1 (0.47) HSPD1BLMHSPE1CA2MEN1
SCHEMBL9516374 0.88 HSPD1 (0.63) HSPD1BLMHSPE1CA2MEN1
SCHEMBL9513919 0.88 HSPD1 (0.63) HSPD1BLMHSPE1CA2MEN1
SCHEMBL9724548 0.88 HSPD1 (0.63) HSPD1BLMHSPE1CA2MEN1
SCHEMBL9513929 0.86 HSPD1 (0.66) HSPD1BLMHSPE1CA2MEN1
SCHEMBL9516386 0.86 HSPD1 (0.66) HSPD1BLMHSPE1CA2MEN1

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
EP-0527165-A1 USE OF METAL SOAPS OF POLYCARBOXYLIC ACIDS OR POLYCARBOXYLIC ACID PARTIAL ESTERS AS PROCESSING AIDS FOR POLYESTERS Henkel Kommanditgesellschaft auf Aktien (DE) 1993-02-17 EP disclosed
WO-1991017208-A1 USE OF METAL SOAPS OF POLYCARBOXYLIC ACIDS OR POLYCARBOXYLIC ACID PARTIAL ESTERS AS PROCESSING AIDS FOR POLYESTERS HENKEL KOMMANDITGESELLSCHAFT AUF AKTIEN (DE) 1991-11-14 WO disclosed