Nafamostat

Nafamostat

SCHEMBL564665

CS(=O)(=O)O.N=C(N)Nc1ccc(C(=O)Oc2ccc3cc(C(=N)N)ccc3c2)cc1

nearest known ligand 0.70

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of Nafamostat. 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
F2 known ✓ P00734 9/20 0.64
CHRM1 known ✓ P11229 1/20 0.58
DRD2 known ✓ P14416 1/20 0.58
ADRA2B known ✓ P18089 1/20 0.58
ADRA2C known ✓ P18825 1/20 0.58
SLC6A4 known ✓ P31645 1/20 0.58
ADRA1A known ✓ P35348 1/20 0.58
DRD3 known ✓ P35462 1/20 0.58
HTR3A known ✓ P46098 1/20 0.58
SLC6A3 known ✓ Q01959 1/20 0.58
GHSR known ✓ Q92847 1/20 0.58
FTO Q9C0B1 1/20 0.70
PRSS1 P07477 10/20 0.64
KLKB1 P03952 8/20 0.64
KLK1 P06870 3/20 0.64
F10 P00742 3/20 0.64
C1R P00736 2/20 0.64
PLG P00747 10/20 0.58
F12 P00748 6/20 0.58
HGFAC Q04756 2/20 0.58

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
Nafamostat SCHEMBL29832433 1.00 FTO (0.70) FTOPRSS1F2KLKB1KLK1
Nafamostat SCHEMBL1568755 1.00 FTO (0.70) FTOPRSS1F2KLKB1KLK1
Nafamostat SCHEMBL874941 0.95 FTO (0.64) FTOPRSS1F2KLKB1KLK1
Nafamostat SCHEMBL135503 0.94 PRSS1 (0.64) FTOPRSS1F2KLKB1KLK1
Nafamostat SCHEMBL29429445 0.94 PRSS1 (0.64) FTOPRSS1F2KLKB1KLK1
Nafamostat SCHEMBL16069975 0.94 PRSS1 (0.64) FTOPRSS1F2KLKB1KLK1
Nafamostat SCHEMBL29429443 0.94 PRSS1 (0.64) FTOPRSS1F2KLKB1KLK1
Nafamostat SCHEMBL3302794 0.93 PRSS1 (0.63) FTOPRSS1F2KLKB1KLK1
Nafamostat SCHEMBL7345508 0.91 PRSS1 (0.62) FTOPRSS1F2KLKB1KLK1
Nafamostat SCHEMBL7338487 0.90 FTO (0.58) FTOPRSS1F2KLKB1KLK1

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 1552 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120771360-B Composite anticoagulation coating and preparation method and application thereof Nanjing Hanke Mingde Medical Technology Co.,Ltd. (CN) 2026-05-26 CN claimed
CN-118439976-B Nafamostat mesylate crystal form and preparation method thereof 南京海纳医药科技股份有限公司 2026-05-12 CN claimed
CN-118576762-B Double-layer core-shell structure artificial fiber dura mater for spinal cord injury and preparation method thereof 山东大学齐鲁医院 2026-05-12 CN claimed
WO-2026089565-A1 USE OF CATHEPSIN L INHIBITOR IN COMBINATION ADMINISTRATION 연세대학교 산학협력단 2026-04-30 WO claimed
US-20250375413-A1 METHOD OF INHIBITING LIPASE ACTIVITY IN AGING UNIV CALIFORNIA (US) 2025-12-11 US claimed
US-20250345458-A1 COMPLEXING AGENT SALT FORMULATIONS OF PHARMACEUTICAL COMPOUNDS AT LOW STOICHIOMETRIC RATIOS BEXSON BIOMEDICAL INC (US) 2025-11-13 US claimed
US-20250188022-A1 PROCESS FOR THE PREPARATION OF NAFAMOSTAT, CAMOSTAT AND THEIR DERIVATIVES COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2025-06-12 US claimed
US-20250152748-A1 HYDRODYNAMIC GENE DELIVERY UNIV JOHNS HOPKINS (US) 2025-05-15 US claimed
US-20250099412-A1 METHOD OF INHIBITING DEGRADING PROTEASE ACTIVITY IN AGING THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2025-03-27 US claimed
EP-4525916-A1 COMPLEXING AGENT SALT FORMULATIONS OF PHARMACEUTICAL COMPOUNDS AT LOW STOICHIOMETRIC RATIOS Bexson Biomedical, Inc. (US) 2025-03-26 EP claimed
US-20050228001-A1 Methods and compositions for treating platelet-related disorders COMERICA BANK 2005-10-13 US claimed
EP-1553091-A1 HETEROAROMATIC PENTACYCLIC COMPOUND AND MEDICINAL USE THEREOF JAPAN TOBACCO INC. (JP) 2005-07-13 EP claimed
CN-1504580-A Combination comprising thrombin agent and examining agent 希森美康株式会社 2004-06-16 CN claimed
EP-1353694-A2 COMBINATIONS OF STEROL ABSORPTION INHIBITOR(S) WITH BLOOD MODIFIER(S) FOR TREATING VASCULAR CONDITIONS Schering Corporation (US) 2003-10-22 EP claimed
US-20020147184-A1 Combinations of sterol absorption inhibitor(s) with blood modifier(s) for treating vascular conditions SCHERING CORPORATION 2002-10-10 US claimed
WO-2002058734-A2 COMBINATIONS OF STEROL ABSORPTION INHIBITOR(S) WITH BLOOD MODIFIER(S) FOR TREATING VASCULAR CONDITIONS SCHERING CORPORATION (US) 2002-08-01 WO claimed
EP-0801953-B1 Medical device for the extracorporal blood or plasma treatment and methods for the manufacture of such device HOSPAL IND (FR) 2002-07-03 EP claimed
US-6248238-B1 SEMIPERMEABLE MEMBRANE CONSISTING OF A NEGATIVELY SURFACE-CHARGED ELECTRONEGATIVE POLYMER HAVING ADSORBED THEREON BEFORE STERILIZATION A CATIONIC PROTEASE INHIBITOR TO PREVENT KALLIKREIN-KININ ACTIVATION DURING DIALYSIS HOSPAL INDUSTRIE (FR) 2001-06-19 US claimed
US-5709993-A Process for anticoagulation during extracorporeal blood circulation sequentially using citrate or nafamostat and heparin BUTUROVIC-PONIKVAR JADRANKA (SI) 1998-01-20 US claimed
WO-1996002288-A1 PROCESS FOR PREVENTING ACTIVATION OF ENZYME SYSTEMS IN HAEMODIALYSIS AND IN SIMILAR PROCEDURES WITH EXTRACORPOREAL BLOOD CIRCULATION BUTUROVIC PONIKVAR JADRANKA (SI) 1996-02-01 WO 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 (3 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 1213/4885CHRM1 2852/4885DRD2 3619/4885
US-20020147184-A1 Combinations of sterol absorption inhibitor(s) with blood modifier(s) for treating vascular conditions APOB, FABP2, CYP46A1 F2 314/4885CHRM1 2836/4885DRD2 4607/4885
US-20250345458-A1 COMPLEXING AGENT SALT FORMULATIONS OF PHARMACEUTICAL COMPOUNDS AT LOW STOICHIOMETRIC RATIOS MC2R, SLC26A3, SLC5A1 F2 1323/4885CHRM1 4393/4885DRD2 2455/4885

“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.