Apraclonidine

Apraclonidine

SCHEMBL41138

Cl.Nc1cc(Cl)c(N=C2NCCN2)c(Cl)c1

nearest known ligand 0.39

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA2AADRA2BADRA2C

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

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
ADRA2A known ✓ P08913 1/20 0.37
ADRA2B known ✓ P18089 1/20 0.37
ADRA2C known ✓ P18825 1/20 0.37
BLM P54132 1/20 0.39
CYP3A4 P08684 3/20 0.38
ALDH1A1 P00352 1/20 0.38
TSHR P16473 2/20 0.37
NFKB1 P19838 1/20 0.37
ADRA1D P25100 1/20 0.37
ADRA1A P35348 1/20 0.37
ADRA1B P35368 1/20 0.37
HSD17B10 Q99714 1/20 0.37
THRB P10828 1/20 0.35
TP53 P04637 1/20 0.30

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
Apraclonidine SCHEMBL8762489 1.00 BLM (0.39) BLMCYP3A4ALDH1A1TSHRADRA2A
Apraclonidine SCHEMBL34127 0.98 CYP3A4 (0.39) BLMCYP3A4ALDH1A1TSHRADRA2A
Apraclonidine SCHEMBL20840496 0.98 CYP3A4 (0.39) BLMCYP3A4ALDH1A1TSHRADRA2A
Apraclonidine SCHEMBL22616253 0.96 CYP3A4 (0.38) BLMCYP3A4ALDH1A1TSHRADRA2A
Apraclonidine SCHEMBL22616315 0.88 THRB (0.34) BLMCYP3A4ALDH1A1TSHRADRA2A
Apraclonidine SCHEMBL22616231 0.88 THRB (0.42) BLMCYP3A4ALDH1A1TSHRADRA2A
Apraclonidine SCHEMBL8891156 0.88 THRB (0.34) BLMCYP3A4ALDH1A1TSHRADRA2A
Apraclonidine SCHEMBL22616102 0.87 THRB (0.41) BLMCYP3A4ALDH1A1TSHRADRA2A
Apraclonidine SCHEMBL22616234 0.85 THRB (0.32) BLMCYP3A4ALDH1A1TSHRADRA2A
Apraclonidine SCHEMBL22616133 0.83 KDM1A (0.32) TSHRADRA2AADRA2BADRA2CNFKB1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4683616-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING APRACLONIDINE FOR OCULAR REDNESS RELIEF Alcon Inc. (CH) 2026-01-28 EP claimed
WO-2024194763-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING APRACLONIDINE FOR OCULAR REDNESS RELIEF ALCON INC. (CH) 2024-09-26 WO claimed
US-20240307355-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING APRACLONIDINE FOR OCULAR REDNESS RELIEF ALCON RESEARCH, LLC 2024-09-19 US claimed
US-20240282425-A1 AUTHENTICATION METHODS AND SYSTEMS FOR DISPENSED PRESCRIPTIONS LOW GORDON KEITH (US) 2024-08-22 US claimed
US-11206977-B2 Vision test for determining retinal disease progression THE TRUSTEES OF THE UNIVERSITY OF PENNYSLVANIA (US) 2021-12-28 US claimed
WO-2020222192-A1 METHODS OF TREATING PRURITUS CLEXIO BIOSCIENCES LTD. (IL) 2020-11-05 WO claimed
WO-2020018498-A1 CYCLODEXTRIN FORMULATIONS ALDEYRA THERAPEUTICS, INC. (US) 2020-01-23 WO claimed
CN-104557716-B A kind of α23 adrenergic receptor agonists Apraclonidine Hydrochloride and preparation method thereof 东华大学 2017-12-22 CN claimed
US-20170354324-A1 VISION TEST FOR DETERMINING RETINAL DISEASE PROGRESSION THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA 2017-12-14 US claimed
US-9371387-B2 Composition for prevention or treatment of ischemic cardiac disease, comprising inhibitor against age-albumin synthesis or release of mononuclear phagocyte system cells as active ingredient GACHON UNIVERSITY OF INDUSTRY-ACADEMIC COOPERATION FOUNDATION (KR) 2016-06-21 US claimed
WO-2010129294-A2 SMALL MOLECULES SUPPORTING PLURIPOTENT CELL GROWTH AND METHODS THEREOF SCHULZ THOMAS C (US) 2010-11-11 WO claimed
US-20060024365-A1 Novel dosage form VAYA NAVIN 2006-02-02 US claimed
US-20060018934-A1 Novel drug delivery system TORRENT PHARMACEUTICALS LIMITED (IN) 2006-01-26 US claimed
US-20060018933-A1 Novel drug delivery system TORRENT PHARMACEUTICALS LIMITED (IN) 2006-01-26 US claimed
EP-0983060-A4 SOLID POROUS MATRICES AND METHODS OF MAKING AND USING THE SAME IMARX PHARMACEUTICAL CORP (US) 2002-04-24 EP claimed
US-20020039594-A1 SOLID POROUS MATRICES AND METHODS OF MAKING AND USING THE SAME IMARX THERAPEUTICS, INC. 2002-04-04 US claimed
EP-0983060-A1 SOLID POROUS MATRICES AND METHODS OF MAKING AND USING THE SAME IMARX PHARMACEUTICAL CORP. (US) 2000-03-08 EP claimed
WO-1998051282-A1 SOLID POROUS MATRICES AND METHODS OF MAKING AND USING THE SAME IMARX PHARMACEUTICAL CORP. (US) 1998-11-19 WO claimed
US-5612364-A INTRAOCULAR HYPERTENSION ALCON LABORATORIES, INC. (US) 1997-03-18 US claimed
US-5212168-A Corticosteriod, beta adrenergic agent NEW ENGLAND MEDICAL CENTER HOSPITAL, INC. (US) 1993-05-18 US 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 (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-20020039594-A1 SOLID POROUS MATRICES AND METHODS OF MAKING AND USING THE SAME EXOSC9, EXOSC5, EXOSC4 ADRA2A 545/4885ADRA2B 994/4885ADRA2C 1114/4885

“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.