SCHEMBL358582

SCHEMBL358582

Cc1ccc([S+](N)[O-])cc1

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ACHE P22303 7/20 0.44
TDP1 Q9NUW8 1/20 0.44
CA1 P00915 2/20 0.39
CA2 P00918 2/20 0.39
CA7 P43166 2/20 0.39
CA9 Q16790 2/20 0.39
CA12 O43570 1/20 0.39
CA3 P07451 1/20 0.39
CA6 P23280 1/20 0.39
CA5A P35218 1/20 0.39
CA5B Q9Y2D0 1/20 0.39
GAA P10253 1/20 0.36
ALDH1A1 P00352 2/20 0.35
HSD17B10 Q99714 1/20 0.33
CYP1A2 P05177 1/20 0.33
CYP2A6 P11509 1/20 0.33
TAAR1 Q96RJ0 1/20 0.33
TLR9 Q9NR96 1/20 0.32
TEAD4 Q15561 1/20 0.32
AGXT P21549 1/20 0.32

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
SCHEMBL1645074 1.00 ACHE (0.44) ACHETDP1CA1CA2CA7
SCHEMBL758088 1.00 ACHE (0.44) ACHETDP1CA1CA2CA7
SCHEMBL22106133 0.78 PARP10 (0.54) ALDH1A1AGXT
SCHEMBL563967 0.77 ACHE (0.50) ACHETDP1CA1CA2CA7
SCHEMBL235851 0.77 ACHE (0.50) ACHETDP1CA1CA2CA7
SCHEMBL4401131 0.77 ACHE (0.50) ACHETDP1CA1CA2CA7
SCHEMBL12903527 0.74 MEN1 (0.47) ACHETDP1CA1CA2CA7
SCHEMBL254471 0.74 ACHE (0.47) ACHETDP1CA1CA2CA7
SCHEMBL280535 0.74 ACHE (0.47) ACHETDP1CA1CA2CA7
SCHEMBL1094237 0.74 ACHE (0.47) ACHETDP1CA1CA2CA7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117865859-A Preparation method of enantiomerically pure p-toluenesulfonamide 常州琦诺生物科技有限公司 2024-04-12 CN claimed
WO-2023227996-A1 A DEUTERATED AMINE COMPOUNDS AND PROCESS FOR SYNTHESIS THEREOF CLEARSYNTH LABS LIMITED (IN) 2023-11-30 WO claimed
CN-116924974-A Preparation method of fluopicolide 天津均凯农业科技有限公司 2023-10-24 CN claimed
CN-113620769-B Preparation method of terpinolene 万华化学集团股份有限公司 2022-07-12 CN claimed
CN-108963389-B Gelable system for lithium-air battery and preparation method and application thereof 北京师范大学 2020-11-13 CN claimed
CN-108440349-B Preparation method of chiral optical pure p-toluenesulfinamide 上海李氏化学科技有限公司 2020-10-20 CN claimed
CN-108558714-B Preparation method of chiral optical pure p-toluenesulfinamide 上海李氏化学科技有限公司 2020-10-16 CN claimed
CN-108484455-B Method for synthesizing chiral optical pure p-toluenesulfinamide 浙江凯普化工有限公司 2020-09-01 CN claimed
CN-108558714-A A kind of chirality optical voidness is to the preparation method of toluenesulfinamide 上海晋鲁医药科技有限公司 2018-09-21 CN claimed
CN-108484455-A A kind of method of synthesis of chiral optical voidness to toluenesulfinamide 上海晋鲁医药科技有限公司 2018-09-04 CN claimed
US-7476762-B2 Methods for preparing sulfonamide compounds WYETH (US) 2009-01-13 US claimed
US-20070293680-A1 For the preparation of (R)-(+)-6-[amino(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl) methyl]-4-(3-chlorophenyl)-1-methyl2(1H)-quinolinone; farnesyl tranferase inhibitory activity JANSSEN PHARMACEUTICA N.V. (BE) 2007-12-20 US claimed
US-20070254929-A1 Fluoro-and trifluoroalkyl-containing heterocyclic sulfonamide inhibitors of beta amyloid production and derivatives thereof WYETH (US) 2007-11-01 US claimed
US-20070249723-A1 Methods for preparing sulfonamide compounds WYETH (US) 2007-10-25 US claimed
EP-1756085-A1 DIASTEREOSELECTIVE SYNTHESIS PROCESS WITH 6-BROMO-4-(3-CHLOROPHENYL)-2-METHOXY-QUINOLINE JANSSEN PHARMACEUTICA N.V. (BE) 2007-02-28 EP claimed
EP-1608638-A1 FLUORO-AND TRIFLUOROALKYL-CONTAINING HETEROCYCLIC SULFONAMIDE INHIBITORS OF BETA AMYLOID PRODUCTION AND DERIVATIVES THEREOF Wyeth (US) 2005-12-28 EP claimed
WO-2005105783-A1 DIASTEREOSELECTIVE SYNTHESIS PROCESS WITH 6-BROMO-4-(3-CHLOROPHENYL)-2-METHOXY-QUINOLINE JANSSEN PHARMACEUTICA N.V. (BE) 2005-11-10 WO claimed
WO-2004092155-A1 FLUORO-AND TRIFLUOROALKYL-CONTAINING HETEROCYCLIC SULFONAMIDE INHIBITORS OF BETA AMYLOID PRODUCTION AND DERIVATIVES THEREOF WYETH (US) 2004-10-28 WO claimed
US-20040198778-A1 Fluoro- and trifluoroalkyl-containing heterocyclic sulfonamide inhibitors of beta amyloid production and derivatives thereof WYETH 2004-10-07 US claimed
EP-0450487-A1 Benzoxazine derivatives, method for their preparation and their use for treating or prophylaxis of diseases HOECHST AKTIENGESELLSCHAFT (DE) 1991-10-09 EP claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 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-20070254929-A1 Fluoro-and trifluoroalkyl-containing heterocyclic sulfonamide inhibitors of beta amyloid production and derivatives thereof SCN8A, CHD8, CHRNA7 ACHE 806/4885TDP1 3059/4885CA1 707/4885
US-20070249723-A1 Methods for preparing sulfonamide compounds PNISR, RRM1, MRPS27 ACHE 2489/4885TDP1 3155/4885CA1 2520/4885
US-20040198778-A1 Fluoro- and trifluoroalkyl-containing heterocyclic sulfonamide inhibitors of beta amyloid production and derivatives thereof BACE1, APP, PSEN1 ACHE 501/4885TDP1 722/4885CA1 298/4885
US-20070293680-A1 For the preparation of (R)-(+)-6-[amino(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl) methyl]-4-(3-chlorophenyl)-1-methyl2(1H)-quinolinone; farnesyl tranferase inhibitory activity FNTB, CYP4F2, FNTA ACHE 2039/4885TDP1 3429/4885CA1 3790/4885

“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.