Candesartan

Candesartan

SCHEMBL40832

CCOc1nc2cccc(C(=O)O)c2n1Cc1ccc(-c2ccccc2-c2nn[nH]n2)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

AGTR1

The experimentally established mechanism targets of Candesartan. 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
AGTR1 known ✓ P30556 1/20 1.00
ABCB11 O95342 1/20 1.00
EGFR P00533 1/20 1.00
ERBB2 P04626 1/20 1.00
CYP3A4 P08684 1/20 1.00
ADORA3 P0DMS8 1/20 1.00
CYP2C9 P11712 1/20 1.00
ADRB3 P13945 1/20 1.00
ADRA2B P18089 1/20 1.00
SLC6A2 P23975 1/20 1.00
TBXAS1 P24557 1/20 1.00
HTR2C P28335 1/20 1.00
PPARG P37231 1/20 1.00
HTR2B P41595 1/20 1.00
AGTR2 P50052 1/20 1.00
PDE3A Q14432 1/20 1.00
LTB4R2 Q9NPC1 1/20 1.00

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
Candesartan SCHEMBL29687505 1.00 ABCB11 (1.00) ABCB11EGFRERBB2CYP3A4ADORA3
SCHEMBL29726879 0.94 AGTR1 (0.88) ABCB11EGFRERBB2CYP3A4ADORA3
SCHEMBL21083737 0.94 AGTR1 (0.88) ABCB11EGFRERBB2CYP3A4ADORA3
SCHEMBL20257353 0.93 CYP3A4 (0.87) ABCB11EGFRERBB2CYP3A4ADORA3
SCHEMBL13707307 0.92 CYP3A4 (0.86) ABCB11EGFRERBB2CYP3A4ADORA3
SCHEMBL2624570 0.92 AGTR1 (0.85) ABCB11EGFRERBB2CYP3A4ADORA3
SCHEMBL21084006 0.91 AGTR1 (0.83) ABCB11EGFRERBB2CYP3A4ADORA3
SCHEMBL21083993 0.90 AGTR1 (0.80) ABCB11EGFRERBB2CYP3A4ADORA3
SCHEMBL2624575 0.88 AGTR1 (0.79) ABCB11EGFRERBB2CYP3A4ADORA3
SCHEMBL21083591 0.88 AGTR1 (0.78) ABCB11EGFRERBB2CYP3A4ADORA3

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 12535 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4710928-A2 METHODS OF TREATING IGA NEPHROPATHY WITH ATRASENTAN Chinook Therapeutics, Inc. (US) 2026-03-18 EP claimed
US-20260048013-A1 PHARMACEUTICAL FORMULATION WITH IMPROVED SOLUBILITY AND BIOAVAILABILITY CONSEJO SUPERIOR INVESTIGACION (ES) 2026-02-19 US claimed
EP-4691556-A2 HUMANIZED ANTI-ACTH ANTIBODIES AND USE THEREOF H. Lundbeck A/S (DK) 2026-02-11 EP claimed
US-20260027215-A1 COMPOSITIONS FOR TRANSPORT OF THERAPEUTIC CARGOS USING BINDERS TARGETING CA-IV RECEPTIVE BIO INC (US) 2026-01-29 US claimed
EP-4076652-B1 A PHARMACEUTICALLY ACCEPTABLE SALT OF ATRASENTAN FOR USE IN A METHOD OF TREATING IGA NEPHROPATHY CHINOOK THERAPEUTICS INC (US) 2025-12-03 EP claimed
US-20250352511-A1 METHODS OF TREATING FOCAL SEGMENTAL GLOMERULOSCLEROSIS WITH ATRASENTAN CHINOOK THERAPEUTICS INC (US) 2025-11-20 US claimed
US-20250339399-A1 SUPRAMOLECULAR SELF-ASSEMBLY SYSTEM BEIJING CREATRON INSTITUTE OF PHARMACEUTICAL RES CO LTD (CN) 2025-11-06 US claimed
EP-4638742-A1 COMPOSITIONS AND METHODS FOR INHIBITING EXPRESSION OF 17BETA-HYDROXYSTEROID DEHYDROGENASE TYPE 13 (HSD17B13) Shanghai Argo Biopharmaceutical Co., Ltd. (CN) 2025-10-29 EP claimed
US-12409173-B2 Repurposing FDA-approved drugs as a novel cancer therapeutic avenue through inhibition of PRMT5 THE TRUSTEES OF INDIANA UNIVERSITY (US) 2025-09-09 US claimed
CN-120142485-A Detection method of impurity hydrazine hydrate in candesartan cilexetil intermediate 珠海润都制药股份有限公司 2025-06-13 CN claimed
CN-1192697-A Epoxy-steroidal aldosterone antagonist and angiotensin II antagonist combination therapy for the treatment of congestive heart failure SEARLE & CO (US) 1998-09-09 CN claimed
WO-1998030216-A1 USE OF ANGIOTENSIN II ANTAGONISTS TO TREAT SYMPTOMATIC HEART FAILURE MERCK & CO., INC. (US) 1998-07-16 WO claimed
EP-0835106-A1 METHOD OF TREATING RENAL DISEASE USING AN ACE INHIBITOR AND AN AII ANTAGONIST MERCK & CO. INC. (US) 1998-04-15 EP claimed
EP-0831911-A2 SPIRONOLACTONE AND ANGIOTENSIN II ANTAGONIST COMBINATION THERAPY FOR TREATMENT OF CONGESTIVE HEART FAILURE G.D. SEARLE & CO. (US) 1998-04-01 EP claimed
EP-0831910-A1 EPOXY-STEROIDAL ALDOSTERONE ANTAGONIST AND ANGIOTENSIN II ANTAGONIST COMBINATION THERAPY FOR TREATMENT OF CONGESTIVE HEART FAILURE G.D. SEARLE & CO. (US) 1998-04-01 EP claimed
WO-1997002032-A1 METHOD OF TREATING RENAL DISEASE USING AN ACE INHIBITOR AND AN AII ANTAGONIST MERCK & CO., INC. (US) 1997-01-23 WO claimed
WO-1996040256-A1 METHOD TO TREAT CARDIOFIBROSIS WITH A COMBINATION OF AN ANGIOTENSIN II ANTAGONIST AND SPIRONOLACTONE G.D. SEARLE & CO. (US) 1996-12-19 WO claimed
WO-1996040258-A2 SPIRONOLACTONE AND ANGIOTENSIN II ANTAGONIST COMBINATION THERAPY FOR TREATMENT OF CONGESTIVE HEART FAILURE G.D. SEARLE & CO. (US) 1996-12-19 WO claimed
WO-1996040257-A1 EPOXY-STEROIDAL ALDOSTERONE ANTAGONIST AND ANGIOTENSIN II ANTAGONIST COMBINATION THERAPY FOR TREATMENT OF CONGESTIVE HEART FAILURE G.D. SEARLE & CO. (US) 1996-12-19 WO claimed
WO-1996040255-A2 METHOD TO TREAT CARDIOFIBROSIS WITH A COMBINATION THERAPY OF AN ANGIOTENSIN II ANTAGONIST AND AN EPOXY-STEROIDAL ALDOSTERONE ANTAGONIST G.D. SEARLE & CO. (US) 1996-12-19 WO claimed