SCHEMBL7342004

SCHEMBL7342004

CS(=O)(=O)O.N=C(N)c1ccc2cc(O)ccc2c1

nearest known ligand 0.77

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 17)

geneUniProtsupporting neighboursconfidence
F2 known ✓ P00734 6/20 0.53
F12 P00748 1/20 0.77
PLAU P00749 15/20 0.57
PLG P00747 8/20 0.53
KLKB1 P03952 7/20 0.53
PRSS1 P07477 7/20 0.53
KLK1 P06870 2/20 0.53
FTO Q9C0B1 1/20 0.52
PLAT P00750 5/20 0.48
LMNA P02545 1/20 0.47
MEN1 O00255 1/20 0.44
NPC1 O15118 1/20 0.44
RAB9A P51151 1/20 0.44
KMT2A Q03164 1/20 0.44
CLK1 P49759 1/20 0.44
DYRK1A Q13627 1/20 0.44
DYRK1B Q9Y463 1/20 0.44

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
SCHEMBL29568370 1.00 F12 (0.77) F12PLAUPLGKLKB1PRSS1
SCHEMBL29934139 1.00 F12 (0.77) F12PLAUPLGKLKB1PRSS1
SCHEMBL29568530 0.88 F12 (1.00) F12PLAUPLGKLKB1PRSS1
SCHEMBL3301671 0.88 F12 (1.00) F12PLAUPLGKLKB1PRSS1
SCHEMBL31499215 0.88 F12 (1.00) F12PLAUPLGKLKB1PRSS1
Hydrochloric Acid SCHEMBL7837112 0.86 F12 (0.96) F12PLAUPLGKLKB1PRSS1
SCHEMBL10938172 0.77 FTO (0.66) F12PLAUPLGKLKB1PRSS1
SCHEMBL31266874 0.75 FTO (0.54) F12PLAUPLGKLKB1PRSS1
SCHEMBL7342007 0.75 FTO (0.54) F12PLAUPLGKLKB1PRSS1
SCHEMBL7338895 0.75 NSD2 (0.45) F12MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119504499-A Synthesis method of 6-amidino-2-naphthol mesylate 江苏杜瑞制药有限公司 2025-02-25 CN claimed
CN-119390614-A Preparation method of nafamostat mesylate 河北广祥制药有限公司 2025-02-07 CN claimed
CN-119143634-A Preparation method of nafamostat mesylate 北京诺康达医药科技股份有限公司 2024-12-17 CN claimed
CN-117185963-A Preparation method of high-purity nafamostat mesylate 华仁药业(日照)有限公司 2023-12-08 CN claimed
CN-116479485-B High-reliability lead frame and preparation method thereof 泰州东田电子有限公司 2023-10-20 CN claimed
CN-116479485-A High-reliability lead frame and preparation method thereof 泰州东田电子有限公司 2023-07-25 CN claimed
WO-2022164150-A1 NAFAMOSTAT MESYLATE AND METHOD FOR PRODUCING INTERMEDIATE THEREOF (주)국전약품 2022-08-04 WO claimed
CN-110330447-B Preparation method and application of nafamostat mesylate intermediate 北京赛升药业股份有限公司 2022-04-15 CN claimed
CN-102225903-B Amidino guanido substituted aromatic heterocyclic copmound and synthesis and use thereof REN JIANDONG 2014-11-26 CN claimed
US-4777182-A ENZYME, HORMONE, COMPLEMENT INHIBITORS TORII & CO., LTD. (JP) 1988-10-11 US claimed
CN-121471113-A Nafamostat medium Process for the preparation of intermediates 鲁南制药集团股份有限公司 2026-02-06 CN disclosed
CN-119390614-B Preparation method of nafamostat mesylate 河北广祥制药有限公司 2025-09-19 CN disclosed
US-20250188022-A1 PROCESS FOR THE PREPARATION OF NAFAMOSTAT, CAMOSTAT AND THEIR DERIVATIVES COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2025-06-12 US disclosed
CN-119504499-A Synthesis method of 6-amidino-2-naphthol mesylate 江苏杜瑞制药有限公司 2025-02-25 CN disclosed
CN-119504499-A Synthesis method of 6-amidino-2-naphthol mesylate 江苏杜瑞制药有限公司 2025-02-25 CN disclosed
US-4563527-A INHIBITORS OF TRYPSIN, PLASMIN, KALLIKREIN, THROMBIN AND COMPLEMENT TORII & CO., LTD. (JP) 1986-01-07 US disclosed
US-4532255-A Amidine compounds and anticomplement agent comprising same TORII & CO., LTD. (JP) 1985-07-30 US disclosed
US-4496584-A ANTITRYPSIN, ANTIKALLIKREIN, ANTITHROMBIN OR ANTIPLASMIN AGENT TORII & CO. LTD. (JP) 1985-01-29 US disclosed
US-4454338-A 6-AMIDINO-2-NATHTHYL-4-GUANIDINOBENZOATE TORII & CO., LTD. (JP) 1984-06-12 US disclosed
EP-0048433-A2 Novel amidine compounds, process for producing same and anti-complement agent comprising them TORII & CO., LTD. (JP) 1982-03-31 EP 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 (1 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-20250188022-A1 PROCESS FOR THE PREPARATION OF NAFAMOSTAT, CAMOSTAT AND THEIR DERIVATIVES TPMT, ADH1C, ADH1A F2 1213/4885F12 925/4885PLAU 374/4885

“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.