SCHEMBL746207

SCHEMBL746207

CCN(CC)CC.CS(=O)(=O)O

nearest known ligand 0.40

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

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
CHRM1 known ✓ P11229 1/20 0.32
NPSR1 Q6W5P4 1/20 0.40
CA2 P00918 3/20 0.37
PAOX Q6QHF9 1/20 0.34
SIGMAR1 Q99720 2/20 0.32
CHRM2 P08172 1/20 0.32
CHRM4 P08173 1/20 0.32
CHRM5 P08912 1/20 0.32
CHRM3 P20309 1/20 0.32
ALDH1A1 P00352 2/20 0.31
KDM4E B2RXH2 1/20 0.31
CYP3A4 P08684 1/20 0.31
CA5A P35218 1/20 0.31
CA5B Q9Y2D0 1/20 0.31
MEN1 O00255 1/20 0.31
HSP90AA1 P07900 1/20 0.31
CYP2C9 P11712 1/20 0.31
HPGD P15428 1/20 0.31
CYP2C19 P33261 1/20 0.31
KMT2A Q03164 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
SCHEMBL28190825 1.00 NPSR1 (0.40) NPSR1CA2PAOXSIGMAR1CHRM2
Hydrochloric Acid SCHEMBL5443087 0.97 NPSR1 (0.39) NPSR1CA2PAOXSIGMAR1CHRM2
Sulfuric Acid SCHEMBL11137355 0.90 NPSR1 (0.46) NPSR1PAOXCHRM2CHRM4CHRM5
Sulfuric Acid SCHEMBL1334876 0.90 NPSR1 (0.46) NPSR1PAOXCHRM2CHRM4CHRM5
Sulfuric Acid SCHEMBL27883463 0.90 NPSR1 (0.46) NPSR1PAOXCHRM2CHRM4CHRM5
Sulfuric Acid SCHEMBL29289482 0.90 NPSR1 (0.46) NPSR1PAOXCHRM2CHRM4CHRM5
Sulfuric Acid SCHEMBL16059228 0.90 NPSR1 (0.46) NPSR1PAOXCHRM2CHRM4CHRM5
Sulfuric Acid SCHEMBL11137352 0.90 NPSR1 (0.46) NPSR1PAOXCHRM2CHRM4CHRM5
Sulfuric Acid SCHEMBL78884 0.90 NPSR1 (0.46) NPSR1PAOXCHRM2CHRM4CHRM5
SCHEMBL28276952 0.89 NPSR1 (0.35) NPSR1CA2PAOX

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3275039-B1 ELECTROLYTES AND METAL HYDRIDE BATTERIES BASF CORP (US) 2025-08-27 EP claimed
CN-115444822-B Ginsenoside epirubicin liposome, and preparation method and application thereof 厦门本素药业有限公司 2024-02-27 CN claimed
CN-115444821-B Ginsenoside vincristine liposome, and preparation method and application thereof 厦门本素药业有限公司 2024-02-27 CN claimed
US-20230018859-A1 ELECTROCHEMICAL SENSORS FOR ANALYTE DETECTION IN WATER AND REFERENCE CORRECTION METHOD BREWER SCIENCE, INC. 2023-01-19 US claimed
WO-2023278877-A1 ELECTROCHEMICAL SENSORS FOR ANALYTE DETECTION IN WATER AND REFERENCE CORRECTION METHOD BREWER SCIENCE, INC. (US) 2023-01-05 WO claimed
WO-2023272962-A1 METHOD FOR DETECTING SMALL POLAR IMPURITIES IN PAZUFLOXACIN MESYLATE BULK DRUG 海南海神同洲制药有限公司 2023-01-05 WO claimed
CN-115518041-A Ginsenoside irinotecan liposome, and preparation method and application thereof 厦门本素药业有限公司 2022-12-27 CN claimed
CN-115487148-A Ginsenoside mitoxantrone liposome, preparation method and application thereof 厦门本素药业有限公司 2022-12-20 CN claimed
CN-115487147-A Ginsenoside adriamycin liposome, preparation method and application thereof 厦门本素药业有限公司 2022-12-20 CN claimed
CN-115444822-A Ginsenoside epirubicin liposome, preparation method and application thereof 厦门本素药业有限公司 2022-12-09 CN claimed
EP-1289637-A4 POLYSULFONAMIDE MATRICES OSMONICS INC (US) 2004-08-18 EP claimed
US-20040007521-A1 Polysulfonamide matrices OSMONICS, INC. 2004-01-15 US claimed
EP-1289637-A2 POLYSULFONAMIDE MATRICES OSMONICS, INC. (US) 2003-03-12 EP claimed
WO-2001091873-A2 POLYSULFONAMIDE MATRICES OSMONICS, INC. (US) 2001-12-06 WO claimed
EP-0577302-B1 Process for preparing alpha-anomer enriched 2-deoxy-2,2-difluoro-D-ribofuranosyl sulfonates LILLY CO ELI (US) 1997-07-16 EP claimed
EP-0640614-B1 Stereoselective process for preparing beta-anomer enriched 2-deoxy-2, 2-difluoro-d-ribofuranosyl-3, 5-hydroxy protected-1-alkyl and aryl sulfonate intermediates LILLY CO ELI (US) 1996-12-04 EP claimed
US-5424416-A Sulfonating a lactol, followed with nucleobase anion, forming anomers ELI LILLY AND COMPANY (US) 1995-06-13 US claimed
EP-0640614-A2 Stereoselective process for preparing beta-anomer enriched 2-deoxy-2, 2-difluoro-d-ribofuranosyl-3, 5-hydroxy protected-1-alkyl and aryl sulfonate intermediates ELI LILLY AND COMPANY (US) 1995-03-01 EP claimed
EP-0577302-A1 Process for preparing alpha-anomer enriched 2-deoxy-2,2-difluoro-D-ribofuranosyl sulfonates ELI LILLY AND COMPANY (US) 1994-01-05 EP claimed
US-5256798-A Treating beta-anomer ribofuranosyl sulfonate with source of conjugate anion ELI LILLY AND COMPANY (US) 1993-10-26 US claimed