SCHEMBL7183393

SCHEMBL7183393

CC(C)(C)C(=O)Oc1ccc(S(=O)(=O)[O-])cc1.[Na+]

nearest known ligand 0.74

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 2)

geneUniProtsupporting neighboursconfidence
ELANE P08246 20/20 0.74
PRTN3 P24158 5/20 0.51

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
SCHEMBL10483727 0.85 ELANE (1.00) ELANEPRTN3
SCHEMBL6337153 0.84 ELANE (0.77) ELANEPRTN3
SCHEMBL22369614 0.82 ELANE (0.86) ELANEPRTN3
SCHEMBL7219090 0.82 ELANE (0.74) ELANEPRTN3
SCHEMBL7183398 0.82 ELANE (0.74) ELANEPRTN3
SCHEMBL31531294 0.82 ELANE (0.74) ELANEPRTN3
SCHEMBL10483766 0.81 ELANE (1.00) ELANEPRTN3
SCHEMBL65265 0.79 MAPT (0.71) ELANE
SCHEMBL30259514 0.79 ELANE (0.70) ELANEPRTN3
SCHEMBL5081863 0.79 POLB (0.48) ELANE

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116874396-A Method for preparing high-purity cilansetron sodium 南京福美瑞信科技有限公司 2023-10-13 CN claimed
CN-113693064-A Disinfectant and preparation method and application thereof 北京擎科生物科技有限公司 2021-11-26 CN claimed
CN-116874396-A Method for preparing high-purity cilansetron sodium 南京福美瑞信科技有限公司 2023-10-13 CN disclosed
CN-113693064-A Disinfectant and preparation method and application thereof 北京擎科生物科技有限公司 2021-11-26 CN disclosed
CN-113693064-A Disinfectant and preparation method and application thereof 北京擎科生物科技有限公司 2021-11-26 CN disclosed
EP-1083167-B1 Process for the preparation of aryl carboxylate esters EASTMAN CHEM CO (US) 2003-04-16 EP disclosed
US-6448430-B1 BY REACTION OF A PHENOL WITH A CARBOXYLIC ACID IN THE PRESENCE OF TRIFLUOROACETIC ACID (TFA) AND TRIFLUOROACETIC ANHYDRIDE (TFAA); RELATIVELY LOW TEMPERATURE EASTMAN CHEMICAL COMPANY 2002-09-10 US disclosed
EP-1083167-A1 Process for the preparation of aryl carboxylate esters EASTMAN CHEMICAL COMPANY (US) 2001-03-14 EP disclosed