Dabuzalgron

Dabuzalgron

SCHEMBL5203336

Cc1c(OCC2=NCCN2)ccc(Cl)c1NS(C)(=O)=O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA1A

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

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
ADRA1A known ✓ P35348 9/20 1.00
NISCH Q9Y2I1 11/20 0.48
HTR1A P08908 4/20 0.43
ADRA2A P08913 4/20 0.43
ADRA2B P18089 4/20 0.43
ADRA2C P18825 4/20 0.43
ADRA1D P25100 3/20 0.41
ADRA1B P35368 3/20 0.41
MAOA P21397 2/20 0.41
MAOB P27338 2/20 0.41
CYP1A2 P05177 1/20 0.40
CYP2D6 P10635 1/20 0.40
THRB P10828 1/20 0.40
TSHR P16473 1/20 0.40
CYP2C19 P33261 1/20 0.40
THPO P40225 1/20 0.40
HSD17B10 Q99714 1/20 0.40

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
Dabuzalgron SCHEMBL19285840 0.99 ADRA1A (0.98) ADRA1ANISCHHTR1AADRA2AADRA2B
Dabuzalgron SCHEMBL5200715 0.99 ADRA1A (0.98) ADRA1ANISCHHTR1AADRA2AADRA2B
SCHEMBL5201030 0.89 ADRA1A (0.80) ADRA1ANISCHHTR1AADRA2AADRA2B
SCHEMBL5200474 0.87 ADRA1A (0.77) ADRA1ANISCHHTR1AADRA2AADRA2B
Hydrochloric Acid SCHEMBL5203525 0.86 ADRA1A (0.75) ADRA1ANISCHHTR1AADRA2AADRA2B
SCHEMBL22596705 0.84 ADRA1A (0.73) ADRA1ANISCHHTR1AADRA2AADRA2B
SCHEMBL5204186 0.80 ADRA1A (0.67) ADRA1ANISCHHTR1AADRA2AADRA2B
SCHEMBL5202260 0.80 ADRA1A (0.66) ADRA1ANISCHHTR1AADRA2AADRA2B
Hydrochloric Acid SCHEMBL5201322 0.79 ADRA1A (0.65) ADRA1ANISCHHTR1AADRA2AADRA2B
SCHEMBL5201551 0.78 ADRA1A (0.64) ADRA1ANISCHHTR1AADRA2AADRA2B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11590107-B2 Methods for treating neurological disorders with α1A-AR partial agonists CURASEN THERAPEUTICS, INC. (US) 2023-02-28 US claimed
US-20220401415-A1 METHODS FOR TREATING NEUROLOGICAL DISORDERS WITH ALPHA1A-AR PARTIAL AGONISTS CURASEN THERAPEUTICS, INC. 2022-12-22 US claimed
EP-4048263-A1 METHODS FOR TREATING NEUROLOGICAL DISORDERS WITH ALPHA 1A-AR PARTIAL AGONISTS Curasen Therapeutics, Inc. (US) 2022-08-31 EP claimed
EP-0887346-B1 N-Phenyl-alkylsulfonamide derivatives, their preparation and their use as alpha1A/1L adrenoceptor agonists HOFFMANN LA ROCHE (CH) 2007-12-12 EP claimed
JP-2007509897-A 2007-04-19 JP claimed
EP-1682110-A1 PHARMACEUTICAL COMPOSITION CONSISTING OF A BETA-3 ADRENOCEPTOR AGONIST AND AN ALPHA AGONIST Boehringer Ingelheim International GmbH (DE) 2006-07-26 EP claimed
US-20050154041-A1 Pharmaceutical composition consisting of a beta-3-adrenoceptor agonist and alpha-agonist BOEHRINGER INGELHEIN INTERNATIONAL GMBH (DE) 2005-07-14 US claimed
WO-2005046664-A1 PHARMACEUTICAL COMPOSITION CONSISTING OF A BETA-3 ADRENOCEPTOR AGONIST AND AN ALPHA AGONIST BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2005-05-26 WO claimed
US-20040170689-A1 Stabilized formulations comprising hydrolytically unstable compositions ODINK DEBRA ALIDA (US) 2004-09-02 US claimed
EP-1341529-A2 HYDROLYTICALLY UNSTABLE COMPOSITIONS F. Hoffman-la Roche AG (CH) 2003-09-10 EP claimed
US-20020086057-A1 Stabilized fromulations comprising hydrolytically unstable compositions SYNTEX (U.S.A.) LLC 2002-07-04 US claimed
WO-2002038133-A2 COMPOSITIONS CONTAINING HYDROLYTICALLY UNSTABLE COMPOUNDS F. HOFFMAN-LA ROCHE AG (CH) 2002-05-16 WO claimed
EP-0887346-A2 Phenyl-and aminophenyl-alkylsulfonamide and urea derivatives, their preparation and their use as alpha1A/1L adrenoceptor agonists F. HOFFMANN-LA ROCHE AG (CH) 1998-12-30 EP claimed
US-20260014159-A1 DEVELOPMENT OF ALPHA-1A-ADRENERGIC RECEPTOR AGONISTS AS A THERAPY TO TREAT HEART FAILURE US GOV VETERANS AFFAIRS (US) 2026-01-15 US disclosed
US-12384751-B2 Allosteric activators of the ALPHA1A-adrenergic receptor THE CLEVELAND CLINIC FOUNDATION (US) 2025-08-12 US disclosed
US-20250188060-A1 ALPHA1A-ADRENERGIC RECEPTOR AGONISTS AND METHODS OF USE CURASEN THERAPEUTICS, INC. 2025-06-12 US disclosed
US-20020086057-A1 Stabilized fromulations comprising hydrolytically unstable compositions SYNTEX (U.S.A.) LLC 2002-07-04 US disclosed
WO-2002038133-A2 COMPOSITIONS CONTAINING HYDROLYTICALLY UNSTABLE COMPOUNDS F. HOFFMAN-LA ROCHE AG (CH) 2002-05-16 WO disclosed
US-6057349-A ALPHA.SUB.1A/1L AGONISTS USED IN THE TREATMENT OF VARIOUS DISEASE STATES SUCH AS URINARY INCONTINENCE, NASAL CONGESTION, PRIAPISM, DEPRESSION, ANXIETY, DEMENTIA, SENILITY, ALZHEIMER'S, DEFICIENCIES IN ATTENTIVENESS AND COGNITION, AND F. HOFFMAN LA ROCHE AG (CH) 2000-05-02 US disclosed
EP-0887346-A2 Phenyl-and aminophenyl-alkylsulfonamide and urea derivatives, their preparation and their use as alpha1A/1L adrenoceptor agonists F. HOFFMANN-LA ROCHE AG (CH) 1998-12-30 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (8 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-20050154041-A1 Pharmaceutical composition consisting of a beta-3-adrenoceptor agonist and alpha-agonist ADRB3, ADRB2, ADRB1 ADRA1A 6/4885NISCH 1361/4885HTR1A 207/4885
US-20020086057-A1 Stabilized fromulations comprising hydrolytically unstable compositions SI, LIPA, HDAC2 ADRA1A 2304/4885NISCH 1994/4885HTR1A 1230/4885
US-12384751-B2 Allosteric activators of the ALPHA1A-adrenergic receptor ADRA1A, ADRB1, ADRA1D ADRA1A 1/4885NISCH 4043/4885HTR1A 13/4885
US-20220401415-A1 METHODS FOR TREATING NEUROLOGICAL DISORDERS WITH ALPHA1A-AR PARTIAL AGONISTS ADRA2A, ADRA1A, HTR1A ADRA1A 2/4885NISCH 1973/4885HTR1A 3/4885
US-11590107-B2 Methods for treating neurological disorders with α1A-AR partial agonists ADRA2A, ADRA1A, HTR1A ADRA1A 2/4885NISCH 2025/4885HTR1A 3/4885
US-20250188060-A1 ALPHA1A-ADRENERGIC RECEPTOR AGONISTS AND METHODS OF USE ADRB1, ADRA1A, ADRA1D ADRA1A 2/4885NISCH 1791/4885HTR1A 41/4885
US-20260014159-A1 DEVELOPMENT OF ALPHA-1A-ADRENERGIC RECEPTOR AGONISTS AS A THERAPY TO TREAT HEART FAILURE ADRB1, ADRA1D, ADRB3 ADRA1A 4/4885NISCH 3782/4885HTR1A 32/4885
US-20040170689-A1 Stabilized formulations comprising hydrolytically unstable compositions SI, LIPA, CEL ADRA1A 2077/4885NISCH 1791/4885HTR1A 1084/4885

“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.