Milrinone

Milrinone

SCHEMBL36947

Cc1[nH]c(=O)c(C#N)cc1-c1ccncc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PDE3A

The experimentally established mechanism targets of Milrinone. 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
PDE3A known ✓ Q14432 12/20 1.00
PDE3B Q13370 11/20 1.00
HPGD P15428 3/20 1.00
KDM4E B2RXH2 3/20 1.00
PDE4A P27815 3/20 1.00
BLM P54132 2/20 1.00
PDE4B Q07343 2/20 1.00
PDE4C Q08493 2/20 1.00
PDE4D Q08499 2/20 1.00
PDE5A O76074 1/20 1.00
LMNA P02545 1/20 1.00
TSHR P16473 1/20 1.00
PTGS1 P23219 1/20 1.00
CYP2C19 P33261 1/20 1.00
GALR3 O60755 1/20 0.73
ALDH1A1 P00352 1/20 0.73
GAA P10253 1/20 0.73
PDE2A O00408 1/20 0.65
PDE1A P54750 1/20 0.65
PDE1B Q01064 1/20 0.65

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
Milrinone SCHEMBL9309054 1.00 PDE3A (1.00) PDE3APDE3BHPGDKDM4EPDE4A
Milrinone SCHEMBL9247989 1.00 PDE3A (1.00) PDE3APDE3BHPGDKDM4EPDE4A
Milrinone SCHEMBL9301167 1.00 PDE3A (1.00) PDE3APDE3BHPGDKDM4EPDE4A
Milrinone SCHEMBL28184205 0.98 PDE3A (0.97) PDE3APDE3BHPGDKDM4EPDE4A
Milrinone SCHEMBL1160021 0.97 PDE3A (0.94) PDE3APDE3BHPGDKDM4EPDE4A
Milrinone SCHEMBL9132559 0.97 PDE3A (0.94) PDE3APDE3BHPGDKDM4EPDE4A
Milrinone SCHEMBL3463564 0.89 PDE3A (0.79) PDE3APDE3BHPGDKDM4EPDE4A
Milrinone SCHEMBL9872022 0.89 PDE3A (0.79) PDE3APDE3BHPGDKDM4EPDE4A
Milrinone SCHEMBL8578994 0.89 PDE3A (0.79) PDE3APDE3BHPGDKDM4EPDE4A
Milrinone SCHEMBL42338 0.89 PDE3A (0.79) PDE3APDE3BHPGDKDM4EPDE4A

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 22004 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120504685-B Prodrug structure with ROS signal response performance, and preparation method and application thereof Rehabilitation University (CN) 2026-05-26 CN claimed
EP-4736841-A1 A MUCOADHESIVE LAYER FOR BUCCAL ADMINISTRATION OF AN ACTIVE PHARMACEUTICAL INGREDIENT IQ medical GmbH (DE) 2026-05-06 EP claimed
EP-4704971-A1 GAMMA STIMULATION AND NEUROMODULATOR COMBINATION THERAPY Cognito Therapeutics, Inc. (US) 2026-03-11 EP claimed
EP-4691556-A2 HUMANIZED ANTI-ACTH ANTIBODIES AND USE THEREOF H. Lundbeck A/S (DK) 2026-02-11 EP claimed
EP-4058037-B1 FIBROBLAST-BASED THERAPY FOR TREATMENT AND PREVENTION OF STROKE SPINALCYTE LLC (US) 2026-01-28 EP claimed
US-12428475-B2 Humanized anti-ACTH antibodies and use thereof H. LUNDBECK A/S (DK) 2025-09-30 US claimed
US-20250285722-A1 SHOCK DETECTION AND MANAGEMENT SYSTEM Nihon Kohden Digital Health Solutions, Inc. (US) 2025-09-11 US claimed
EP-4032401-B1 METHOD FOR PRODUCING AN ORGAN CARE SOLUTION FOR EX-VIVO MACHINE PERFUSION OF DONOR LUNGS TRANSMEDICS INC (US) 2025-09-10 EP claimed
US-20250275952-A1 4-METHYLSULFONYL-SUBSTITUTED PIPERIDINE UREA COMPOUNDS MYOKARDIA INC (US) 2025-09-04 US claimed
US-20250228824-A1 COMPOSITIONS AND METHODS FOR INHIBITION OF ITO AS TREATMENT FOR THE J WAVE SYNDROMES AND HYPOTHERMIA SIMON FRASER UNIVERSITY (CA) 2025-07-17 US claimed
US-4868182-A HYPOTENSIVE AND CARDIOTONIC, SYNERGISTIC MERRELL DOW PHARMACEUTICALS INC. (US) 1989-09-19 US claimed
US-4806361-A THREE ADMIXED POLYMERS SOLUBLE AT DIFFERENT PHS STERLING DRUG INC. (US) 1989-02-21 US claimed
US-4783337-A Osmotic system comprising plurality of members for dispensing drug ALZA CORPORATION (US) 1988-11-08 US claimed
US-4650806-A Cardiotonic 5-(heterylcarbonyl)-pyridones STERLING DRUG INC. (US) 1987-03-17 US claimed
EP-0075116-B1 PROCESS FOR PREPARING 1,2-DIHYDRO-6-METHYL-2-OXO-5-(PYRIDINYL)NICOTINONITRILES STERLING DRUG INC. (US) 1985-05-22 EP claimed
US-4469871-A Process for preparing 2-(lower-alkoxy)-1-(pyridinyl) ethenyl lower-alkyl ketones STERLING DRUG INC. (US) 1984-09-04 US claimed
US-4413127-A Preparation of 1,2-dihydro-6-(lower alkyl)-2-oxo-5-(pyridinyl)nicotinonitriles STERLING DRUG INC. (US) 1983-11-01 US claimed
EP-0075116-A1 Process for preparing 1,2-dihydro-6-methyl-2-oxo-5-(pyridinyl)nicotinonitriles STERLING DRUG INC. (US) 1983-03-30 EP claimed
US-4347363-A Process for preparing 1,2-dihydro-6-methyl-2-oxo-5-(pyridinyl)nicotinonitriles STERLING DRUG INC. (US) 1982-08-31 US claimed
US-4313951-A 3-Substituted-6-(lower-alkyl)-5-(pyridinyl)-2(1H)-pyridinones, their cardiotonic use and intermediates therefor STERLING DRUG INC. (US) 1982-02-02 US claimed