SCHEMBL5529599

SCHEMBL5529599

Cc1onc(NS(=O)(=O)c2ccccc2Br)c1C

nearest known ligand 0.63

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
EDNRA P25101 12/20 0.63
EDNRB P24530 8/20 0.59
BRD4 O60885 1/20 0.51

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
SCHEMBL30171185 1.00 EDNRA (0.63) EDNRAEDNRBBRD4
SCHEMBL30296336 0.86 EDNRA (0.56) EDNRAEDNRBBRD4
SCHEMBL5321684 0.86 EDNRA (0.56) EDNRAEDNRBBRD4
SCHEMBL30844573 0.86 EDNRA (0.56) EDNRAEDNRBBRD4
SCHEMBL5330400 0.86 EDNRA (0.56) EDNRAEDNRBBRD4
SCHEMBL26688897 0.83 EDNRA (0.63) EDNRAEDNRB
SCHEMBL6557303 0.83 EDNRA (0.48) EDNRA
SCHEMBL5324233 0.83 EDNRA (0.56) EDNRAEDNRBBRD4
SCHEMBL29281026 0.82 EDNRA (0.46) EDNRAEDNRB
SCHEMBL29001495 0.81 CCNT1 (0.43) EDNRAEDNRBBRD4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025094214-A1 Process for the preparation of 2-[4-[(2-butyl-4-oxo-1,3-diazaspiro[4.4]non-1-en-3-yl)methyl]-2-(ethoxymethyl)phenyl]-N-(4,5-dimethyl-1,2-oxazol-3-yl) benzenesulfonamide and its intermediates thereof MSN LABORATORIES PRIVATE LIMITED, R&D CENTER (IN) 2025-05-08 WO claimed
WO-2025094214-A1 Process for the preparation of 2-[4-[(2-butyl-4-oxo-1,3-diazaspiro[4.4]non-1-en-3-yl)methyl]-2-(ethoxymethyl)phenyl]-N-(4,5-dimethyl-1,2-oxazol-3-yl) benzenesulfonamide and its intermediates thereof MSN LABORATORIES PRIVATE LIMITED, R&D CENTER (IN) 2025-05-08 WO disclosed
US-20250051315-A1 COMPOUND, ANGIOTENSIN II TYPE 1 RECEPTOR ANTAGONIST AND PHARMACEUTICAL COMPOSITION ALCHEMEDICINE, INC. (JP) 2025-02-13 US disclosed
EP-4458826-A1 COMPOUND, ANGIOTENSIN II TYPE 1 RECEPTOR ANTAGONIST AND PHARMACEUTICAL COMPOSITION Alchemedicine, Inc. (JP) 2024-11-06 EP disclosed
CN-118284605-A Compounds, angiotensin II type 1 receptor antagonists and pharmaceutical compositions 亚克医药株式会社 2024-07-02 CN disclosed
WO-2023224963-A1 DUAL-ACTING ANGIOTENSIN AND ENDOTHELIN RECEPTOR ANTAGONISTS ARIA PHARMACEUTICALS, INC. (US) 2023-11-23 WO disclosed
WO-2023224963-A1 DUAL-ACTING ANGIOTENSIN AND ENDOTHELIN RECEPTOR ANTAGONISTS ARIA PHARMACEUTICALS, INC. (US) 2023-11-23 WO disclosed
WO-2023127853-A1 COMPOUND, ANGIOTENSIN II TYPE 1 RECEPTOR ANTAGONIST, AND PHARMACEUTICAL COMPOSITION 株式会社アークメディスン 2023-07-06 WO disclosed
WO-2023127853-A1 COMPOUND, ANGIOTENSIN II TYPE 1 RECEPTOR ANTAGONIST, AND PHARMACEUTICAL COMPOSITION 株式会社アークメディスン 2023-07-06 WO disclosed
WO-2023066348-A1 DUAL ANTAGONIST AND USE THEREOF 年衍药业(上海)有限公司 2023-04-27 WO disclosed
US-6638937-B2 As antihypertensive agents; for therapy of disorders related to renal, glomerular and mesangial cell function; therapy of endotoxemia or endotoxin shock as well as hemorrhagic shock; useful in alleviation of pain associated cancer BRISTOL-MYERS SQUIBB CO. 2003-10-28 US disclosed
EP-1328523-A2 METHODS FOR THE PREPARATION OF BIPHENYL ISOXAZOLE SULFONAMIDES Bristol-Myers Squibb Company (US) 2003-07-23 EP disclosed
US-20020143024-A1 Biphenyl sulfonamides as dual angiotensin endothelin receptor antagonists PHARMACOPEIA, LLC 2002-10-03 US disclosed
US-20020132838-A1 Methods for the preparation of biphenyl isoxazole sulfonamides BRISTOL-MYERS SQUIBB COMPANY 2002-09-19 US disclosed
EP-1237888-A2 BIPHENYL SULFONAMIDES AS DUAL ANGIOTENSIN ENDOTHELIN RECEPTOR ANTAGONISTS Bristol-Myers Squibb Company (US) 2002-09-11 EP disclosed
WO-2002032884-A2 METHODS FOR THE PREPARATION OF BIPHENYL ISOXAZOLE SULFONAMIDES BRISTOL-MYERS SQUIBB COMPANY (US) 2002-04-25 WO disclosed
WO-2001044239-A2 BIPHENYL SULFONAMIDES AS DUAL ANGIOTENSIN ENDOTHELIN RECEPTOR ANTAGONISTS BRISTOL-MYERS SQUIBB CO. (US) 2001-06-21 WO disclosed
US-6043265-A TREATING HYPERTENSION, PULMONARY HYPERTENSION, BENIGN PROSTATIC HYPERTROPHY, MIGRAINE, UROGENITAL DISORDERS, ENDOTOXEMIA, ISCHEMIA, ATHEROSCLEROSIS, RESTENOSIS, SUBARACHNOID HEMORRHAGE, CONGESTIVE HEART FAILURE BRISTOL-MYERS SQUIBB CO. (US) 2000-03-28 US disclosed
US-5846990-A Substituted biphenyl isoxazole sulfonamides BRISTOL-MYERS SQUIBB CO. (US) 1998-12-08 US disclosed
US-5780473-A Substituted biphenyl sulfonamide endothelin antagonists BRISTOL-MYERS SQUIBB COMPANY (US) 1998-07-14 US 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 (3 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-20020143024-A1 Biphenyl sulfonamides as dual angiotensin endothelin receptor antagonists EDNRB, AGTR2, EDNRA EDNRA 3/4885EDNRB 1/4885BRD4 158/4885
US-20020132838-A1 Methods for the preparation of biphenyl isoxazole sulfonamides REN, STS, CYP4X1 EDNRA 11/4885EDNRB 12/4885BRD4 149/4885
US-20250051315-A1 COMPOUND, ANGIOTENSIN II TYPE 1 RECEPTOR ANTAGONIST AND PHARMACEUTICAL COMPOSITION AGTR1, AGTR2, ADRB1 EDNRA 154/4885EDNRB 216/4885BRD4 915/4885

“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.