Fasudil

Fasudil

SCHEMBL317082

Cl.O=S(=O)(c1cccc2cnccc12)N1CCCNCC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ROCK1ROCK2

The experimentally established mechanism targets of Fasudil. 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
ROCK2 known ✓ O75116 8/20 1.00
ROCK1 known ✓ Q13464 7/20 1.00
CCR2 P41597 2/20 1.00
HTT P42858 2/20 1.00
PRKCE Q02156 6/20 0.98
PRKCD Q05655 6/20 0.98
PRKD1 Q15139 6/20 0.98
CYP3A4 P08684 6/20 0.98
PRKD3 O94806 5/20 0.98
PRKCG P05129 5/20 0.98
PRKCB P05771 5/20 0.98
PRKCA P17252 5/20 0.98
PRKCH P24723 5/20 0.98
PRKCI P41743 5/20 0.98
PRKCQ Q04759 5/20 0.98
PRKCZ Q05513 5/20 0.98
CYP2D6 P10635 5/20 0.98
PRKACA P17612 4/20 0.98
PRKACG P22612 4/20 0.98
PRKACB P22694 4/20 0.98

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
Fasudil SCHEMBL29351490 1.00 ROCK2 (1.00) ROCK2ROCK1CCR2HTTPRKCE
Fasudil SCHEMBL599053 1.00 ROCK2 (1.00) ROCK2ROCK1CCR2HTTPRKCE
Fasudil SCHEMBL29393852 1.00 ROCK2 (1.00) ROCK2ROCK1CCR2HTTPRKCE
Fasudil SCHEMBL30084458 1.00 ROCK2 (1.00) ROCK2ROCK1CCR2HTTPRKCE
Fasudil SCHEMBL6032335 1.00 ROCK2 (1.00) ROCK2ROCK1CCR2HTTPRKCE
Fasudil SCHEMBL30064396 0.99 ROCK2 (0.98) ROCK2ROCK1CCR2HTTPRKCE
Fasudil SCHEMBL6269513 0.99 ROCK2 (0.98) ROCK2ROCK1CCR2HTTPRKCE
Fasudil SCHEMBL4728659 0.99 ROCK2 (0.98) ROCK2ROCK1CCR2HTTPRKCE
Fasudil SCHEMBL4725334 0.99 ROCK2 (0.98) ROCK2ROCK1CCR2HTTPRKCE
Fasudil SCHEMBL2154690 0.99 ROCK2 (0.98) ROCK2ROCK1CCR2HTTPRKCE

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

Appears in 2784 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260144819-A1 NK-92 Cells with Cytokine Induced Memory-Like Cytotoxicity And Derivatives Thereof IMMUNITYBIO, INC. (US) 2026-05-28 US claimed
EP-4739323-A1 <SMALLCAPS/>? ? ?EX VIVO? ? ? ? ?GENERATION OF IMMUNE EFFECTOR CELLS FROM APHERESIS MATERIAL INTERMEDIATES ImmunityBio, Inc. (US) 2026-05-13 EP claimed
US-20260097083-A1 METHOD FOR PRODUCING PANCREATIC ENDODERM CELLS KYOTO UNIVERSITY (JP) 2026-04-09 US claimed
US-20260014167-A1 Treating Amyotrophic Lateral Sclerosis Having Onset 24 Months Prior to Treatment WOOLSEY PHARMACEUTICALS, INC. (US) 2026-01-15 US claimed
EP-4678241-A2 A QUADRICISTRONIC SYSTEM COMPRISING A HOMING RECEPTOR OR A CYTOKINE, AND CHIMERIC ANTIGEN RECEPTOR FOR GENETIC MODIFICATION OF IMMUNOTHERAPIES ImmunityBio, Inc. (US) 2026-01-14 EP claimed
US-12473347-B2 Elimination of PD-L1-positive malignancies by PD-L1 chimeric antigen receptor-expressing NK cells IMMUNITYBIO, INC. (US) 2025-11-18 US claimed
US-12473348-B2 Elimination of PD-L1-positive malignancies by PD-L1 chimeric antigen receptor-expressing NK cells IMMUNITYBIO, INC. (US) 2025-11-18 US claimed
EP-4629995-A1 COMBINATION THERAPY FOR THE TREATMENT OF GLYOBLASTOMA The University of Florida Research Foundation, Inc. (US) 2025-10-15 EP claimed
US-12398370-B2 Culture medium and method for inducing iPSC differentiation to obtain macrophages and use thereof ALLIFE MEDICINE (BEIJING) LIMITED (CN) 2025-08-26 US claimed
EP-4601636-A1 METHOD OF TREATING AMYOTROPHIC LATERAL SCLEROSIS BY ORAL ADMINISTRATION OF FASUDIL Woolsey Pharmaceuticals, Inc. (US) 2025-08-20 EP claimed
WO-2004003170-A2 AGENTS CAPABLE OF INHIBITING RAS AND USES THEREOF THE JOHNS HOPKINS UNIVERSITY (US) 2004-01-08 WO claimed
US-20030139801-A1 Delivery of therapeutic capable agents AVANTEC VASCULAR CORPORATION (US) 2003-07-24 US claimed
US-20030050692-A1 Delivery of therapeutic capable agents AVANTEC VASCULAR CORPORATION 2003-03-13 US claimed
WO-2003009779-A2 DELIVERY OF THERAPEUTIC CAPABLE AGENTS AVANTEC VASCULAR CORPORATION (US) 2003-02-06 WO claimed
WO-2003009777-A2 DELIVERY OF THERAPEUTIC CAPABLE AGENTS AVANTEC VASCULAR CORPORATION (US) 2003-02-06 WO claimed
CN-1307476-A Sustained release oral preparations of fasudil hydrochloride ASAHI CHEMICAL IND (JP) 2001-08-08 CN claimed
EP-1110553-A1 SUSTAINED RELEASE ORAL PREPARATIONS OF FASUDIL HYDROCHLORIDE Asahi Kasei Kabushiki Kaisha (JP) 2001-06-27 EP claimed
EP-1064944-A1 Protein kinase N inhibitor comprising Fasudil SCHERING AKTIENGESELLSCHAFT (DE) 2001-01-03 EP claimed
EP-0845265-A1 MUCOSAL PREPARATION CONTAINING PHYSIOLOGICALLY ACTIVE PEPTIDE Asahi Kasei Kogyo Kabushiki Kaisha (JP) 1998-06-03 EP claimed
EP-0003069-A1 Pseudomonic acid C, pharmaceutically acceptable salts or esters thereof, processes for their preparation and pharmaceutical or veterinary compositions containing them BEECHAM GROUP PLC (GB) 1979-07-25 EP claimed