Rilmenidine

Rilmenidine

SCHEMBL114420

C1COC(NC(C2CC2)C2CC2)=N1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

NISCH

The experimentally established mechanism targets of Rilmenidine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
NISCH known ✓ Q9Y2I1 6/20 1.00
ADRA2A P08913 12/20 1.00
ADRA2B P18089 12/20 1.00
ADRA2C P18825 11/20 1.00
ADRA1A P35348 4/20 1.00
CYP3A4 P08684 2/20 1.00
GMNN O75496 1/20 1.00
CYP1A2 P05177 1/20 1.00
HTR1A P08908 1/20 1.00
CYP2D6 P10635 1/20 1.00
CYP2C9 P11712 1/20 1.00
TSHR P16473 1/20 1.00
OPRK1 P41145 1/20 1.00
HIF1A Q16665 1/20 1.00
KDM4E B2RXH2 1/20 0.73
POLB P06746 1/20 0.73
MAPT P10636 1/20 0.73
NFKB1 P19838 1/20 0.73

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
Rilmenidine SCHEMBL15516636 1.00 ADRA2A (1.00) ADRA2AADRA2BADRA2CNISCHADRA1A
SCHEMBL6368709 0.91 ADRA2A (0.83) ADRA2AADRA2BADRA2CNISCHADRA1A
Rilmenidine SCHEMBL1231349 0.90 ADRA2A (0.81) ADRA2AADRA2BADRA2CNISCHADRA1A
Rilmenidine SCHEMBL6373730 0.86 ADRA2A (0.73) ADRA2AADRA2BADRA2CNISCHADRA1A
Rilmenidine SCHEMBL30892124 0.86 CYP3A4 (1.00) ADRA2AADRA2BADRA2CNISCHADRA1A
SCHEMBL11639239 0.81 ADRA2A (0.68) ADRA2AADRA2BADRA2CNISCHADRA1A
SCHEMBL11668019 0.78 ADRA2A (0.64) ADRA2AADRA2BADRA2CNISCHADRA1A
SCHEMBL11140750 0.77 ADRA2A (0.62) ADRA2AADRA2BADRA2CNISCHADRA1A
SCHEMBL13616145 0.77 ADRA2A (0.62) ADRA2AADRA2BADRA2CNISCHADRA1A
SCHEMBL11638113 0.77 ADRA2A (0.62) ADRA2AADRA2BADRA2CNISCHADRA1A

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 2957 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122047286-A Large-model-based intelligent agent construction framework and behavior simulation method and device 北京华如科技股份有限公司 2026-05-15 CN claimed
EP-4101448-B1 COMPOSITION COMPRISING RILMENIDINE COMPOUND AS ACTIVE INGREDIENT FOR TREATMENT OF FRAGILE X SYNDROME OR RELATED DEVELOPMENTAL DISABILITY NEUROVENTI (KR) 2026-04-22 EP claimed
EP-4704839-A2 IMIDAZOLE CONTAINING COMPOUNDS, DERIVATIVES THEREFORE, AND USES THEREOF ALPHERABIO LLC (US) 2026-03-11 EP claimed
US-12396983-B2 Composition comprising rilmenidine compound as active ingredient for treatment of fragile X syndrome or related developmental disability NEUROVENTI (KR) 2025-08-26 US claimed
US-20250228817-A1 ENHANCING AUTOPHAGY OR INCREASING LONGEVITY BY ADMINISTRATION OF UROLITHINS AMAZENTIS SA (CH) 2025-07-17 US claimed
US-20250213647-A1 CHEMOKINE RECEPTORS AND ALPHA1 ADRENERGIC RECEPTORS/VASOPRESSIN RECEPTORS 1A HETEROMERS AS DRUG TARGETS FOR DISEASE UNIVERSITY OF SOUTH FLORIDA 2025-07-03 US claimed
US-20250177354-A1 THERAPEUTIC COMBINATIONS, COMPOSITIONS, AND METHODS FOR DESIGNING AND PRODUCING ENTACTOGENIC MINDSTATES MINDSTATE DESIGN LABS INC (US) 2025-06-05 US claimed
WO-2025080559-A1 METHODS AND COMPOSITIONS FOR TREATING DRUG OVERDOSE ENALARE THERAPEUTICS INC. (US) 2025-04-17 WO claimed
US-20250114370-A1 METHODS AND COMPOSITIONS FOR TREATING DRUG OVERDOSE ENALARE THERAPEUTICS INC (US) 2025-04-10 US claimed
WO-2025067458-A1 OPHTHALMIC PHARMACEUTICAL COMPOSITION AND USE THEREOF 苏州普乐康医药科技有限公司 2025-04-03 WO claimed
WO-2000021509-A2 METHODS OF TREATMENT IMPERIAL COLLEGE INNOVATIONS LIMITED (GB) 2000-04-20 WO claimed
US-5605911-A NEUROTOXIC SIDE EFFECT INHIBITION WASHINGTON UNIVERSITY (US) 1997-02-25 US claimed
EP-0719139-A1 USE OF CENTRALLY ACTIVE ALPHAAGONISTS FOR INHIBING POSTRAUMATIC METABOLIC STRESS Dr. Karl Thomae GmbH (DE) 1996-07-03 EP claimed
US-5459133-A Methods and products for treating presbyopia TELOR OPHTHALMIC PHARMACEUTICALS, INC. (US) 1995-10-17 US claimed
EP-0643576-A1 ALPHA-2-ADRENERGIC AGONISTS FOR TREATING PRESBYOPIA TELOR OPHTHALMIC PHARMACEUTICALS, INC. (US) 1995-03-22 EP claimed
WO-1995003798-A2 USE OF CENTRALLY EFFECTIVE α-2 AGONISTS FOR INHIBITING POSTAGGRESSION METABOLISM BOEHRINGER INGELHEIM INT (DE) 1995-02-09 WO claimed
WO-1993025199-A1 ALPHA-2-ADRENERGIC AGONISTS FOR TREATING PRESBYOPIA TELOR OPHTHALMIC PHARMACEUTICALS, INC. (US) 1993-12-23 WO claimed
EP-0510052-A1 MEDICAMENT FOR TREATMENT OF HEART FAILURE HEDNER, Thomas (SE) 1992-10-28 EP claimed
WO-1991009627-A1 MEDICAMENT FOR TREATMENT OF HEART FAILURE HEDNER THOMAS (SE) 1991-07-11 WO claimed
US-4102890-A HYPNOTIC, ANALGESIC, HYPOTENSIVE, CARDIOVASCULAR DEPRESSANTS, NEURO-MODULATORS SCIENCE-UNION ET CIE, SOCIETE FRANCAISE DE RECHERCHE MEDICALE (FR) 1978-07-25 US claimed