SCHEMBL3293117

SCHEMBL3293117

CC(N1CCN(C(C)S(=O)(=O)[O-])CC1)S(=O)(=O)[O-].[Na+].[Na+]

nearest known ligand 0.33

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 4)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.33
GAA P10253 1/20 0.33
CHRM2 P08172 1/20 0.30
CHRM1 P11229 1/20 0.30

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
Potassium Ion SCHEMBL5383247 0.95 LMNA (0.33) LMNAGAACHRM2CHRM1
SCHEMBL6873304 0.89 MEN1 (0.32)
SCHEMBL30869985 0.84 L3MBTL1 (0.38) LMNAGAA
SCHEMBL28353920 0.84 CHRM2 (0.41) LMNACHRM2CHRM1
SCHEMBL5497675 0.84 L3MBTL1 (0.38) LMNAGAA
Water SCHEMBL28916298 0.83 L3MBTL1 (0.37) LMNAGAA
SCHEMBL10781958 0.81 CHRM2 (0.48) LMNAGAACHRM2CHRM1
SCHEMBL5492629 0.80 CA12 (0.38) LMNAGAA
Potassium Ion SCHEMBL8985015 0.80 CA12 (0.38) LMNAGAA
Water SCHEMBL28800260 0.72 KDM4E (0.30)

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 21 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11858883-B2 Method for recycling taurine mother liquor QIANJIANG Yongan Phamaceutical CO., LTD. (CN) 2024-01-02 US claimed
US-20230212111-A1 METHOD FOR RECYCLING TAURINE MOTHER LIQUOR QIANJIANG YONGAN PHARMACEUTICAL CO., LTD. (CN) 2023-07-06 US claimed
EP-4201921-A1 METHOD FOR RECYCLING TAURINE MOTHER LIQUOR Qiangjiang Yongan Pharmaceutical Co., Ltd. (CN) 2023-06-28 EP claimed
US-10107736-B2 Hydrogel compositions and methods for electrochemical sensing PORTLAND STATE UNIVERSITY (US) 2018-10-23 US claimed
US-20160123865-A1 HYDROGEL COMPOSITIONS AND METHODS FOR ELECTROCHEMICAL SENSING PORTLAND STATE UNIVERSITY (US) 2016-05-05 US claimed
US-11858883-B2 Method for recycling taurine mother liquor QIANJIANG Yongan Phamaceutical CO., LTD. (CN) 2024-01-02 US disclosed
US-20230212111-A1 METHOD FOR RECYCLING TAURINE MOTHER LIQUOR QIANJIANG YONGAN PHARMACEUTICAL CO., LTD. (CN) 2023-07-06 US disclosed
EP-4201921-A1 METHOD FOR RECYCLING TAURINE MOTHER LIQUOR Qiangjiang Yongan Pharmaceutical Co., Ltd. (CN) 2023-06-28 EP disclosed
US-10107736-B2 Hydrogel compositions and methods for electrochemical sensing PORTLAND STATE UNIVERSITY (US) 2018-10-23 US disclosed
US-20160123865-A1 HYDROGEL COMPOSITIONS AND METHODS FOR ELECTROCHEMICAL SENSING PORTLAND STATE UNIVERSITY (US) 2016-05-05 US disclosed
EP-1828106-B1 METHAMPHETAMINE DERIVATIVES AND CONJUGATES FOR IMMUNOASSAY ROCHE DIAGNOSTICS GMBH (DE) 2012-10-31 EP disclosed
US-7732160-B2 Methamphetamine derivatives and conjugates for immunoassay ROCHE DIAGNOSTICS OPERATIONS, INC. (US) 2010-06-08 US disclosed
US-7294649-B2 Methamphetamine derivatives and conjugates for immunoassay ROCHE DIAGNOSTICS OPERATINS, INC. (US) 2007-11-13 US disclosed
EP-1828106-A2 METHAMPHETAMINE DERIVATIVES AND CONJUGATES FOR IMMUNOASSAY Roche Diagnostics GmbH (DE) 2007-09-05 EP disclosed
US-20070099234-A1 Specific detection of chitin using chitin-binding domain NEW ENGLAND BIOLABS, INC. (US) 2007-05-03 US disclosed
US-7101980-B2 Derivatives, conjugates, and antibodies for detecting ecstasy-class analytes ROCHE DIAGNOSTICS OPERATIONS, INC. (US) 2006-09-05 US disclosed
US-20060134711-A1 Methamphetamine derivatives and conjugates for immunoassay ROCHE DIAGNOSTICS OPERATIONS, INC. 2006-06-22 US disclosed
WO-2006063829-A2 METHAMPHETAMINE DERIVATIVES AND CONJUGATES FOR IMMUNOASSAY ROCHE DIAGNOSTICS GMBH (DE) 2006-06-22 WO disclosed
EP-1498428-A1 Antibodies for detecting ecstasy-class analytes Roche Diagnostics GmbH (DE) 2005-01-19 EP disclosed
US-4247633-A Reagent for colorimetric determination of creative phosphokinase PABST BREWING COMPANY (US) 1981-01-27 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 (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-20060134711-A1 Methamphetamine derivatives and conjugates for immunoassay PNMT, COMT, MCHR1 LMNA 3446/4885GAA 4532/4885CHRM2 13/4885
US-20230212111-A1 METHOD FOR RECYCLING TAURINE MOTHER LIQUOR SLC6A6, SLC6A12, UGT8 LMNA 2929/4885GAA 215/4885CHRM2 4342/4885

“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.