SCHEMBL615804

SCHEMBL615804

COC(=O)c1c[nH]c2ccc([N+](=O)[O-])cc12

nearest known ligand 0.64

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
▸ NR4A2 P43354 5/20 0.63
▸ GABRP O00591 1/20 0.59
▸ GABRD O14764 1/20 0.59
▸ GABRA1 P14867 1/20 0.59
▸ GABRB1 P18505 1/20 0.59
▸ GABRG2 P18507 1/20 0.59
▸ GABRB3 P28472 1/20 0.59
▸ GABRA5 P31644 1/20 0.59
▸ GABRA3 P34903 1/20 0.59
▸ GABRA2 P47869 1/20 0.59
▸ GABRB2 P47870 1/20 0.59
▸ GABRA4 P48169 1/20 0.59
▸ GABRE P78334 1/20 0.59
▸ GABRA6 Q16445 1/20 0.59
▸ GABRG1 Q8N1C3 1/20 0.59
▸ GABRG3 Q99928 1/20 0.59
▸ GABRQ Q9UN88 1/20 0.59

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
SCHEMBL2843412 0.89 NR4A2 (0.63) NR4A2GABRPGABRDGABRA1GABRB1
SCHEMBL28363236 0.86 GABRP (0.63) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL14089124 0.86 NR4A2 (0.63) NR4A2GABRPGABRDGABRA1GABRB1
SCHEMBL28265772 0.86 GABRP (0.53) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL1005283 0.85 GABRP (0.51) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL5213756 0.84 NQO2 (0.57) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL2841773 0.84 GABRP (0.62) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL12501390 0.83 GABRP (0.56) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL13302316 0.82 HTR7 (0.51) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL27693237 0.81 TNFSF11 (0.53) GABRPGABRDGABRA1GABRB1GABRG2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115667216-B (1H-indol-5-yl) acrylamide derivatives as inhibitors of TEAD proteins and HIPPO-YAP1/TAZ signaling cascades for the treatment of cancer 赛诺菲 2025-02-18 — — CN disclosed
EP-4132907-B1 (1H-INDOL-5-YL)ACRYLAMIDE DERIVATIVES AS INHIBITORS OF TEAD PROTEINS AND THE HIPPO-YAP1/TAZ SIGNALING CASCADE FOR THE TREATMENT OF CANCER SANOFI SA (FR) 2024-04-24 — — EP disclosed
US-20230140808-A1 (1 H-Indol-5-YL)Acrylamide Derivatives as Inhibitors of Tead Proteins and the Hippo-YAP1/TAZ Signaling Cascade for the Treatment of Cancer SANOFI (FR) 2023-05-04 — — US disclosed
EP-4132907-A1 (1 H-INDOL-5-YL)ACRYLAMIDE DERIVATIVES AS INHIBITORS OF TEAD PROTEINS AND THE HIPPO-YAP1/TAZ SIGNALING CASCADE FOR THE TREATMENT OF CANCER SANOFI (FR) 2023-02-15 — — EP disclosed
CN-115667216-A (1H-indol-5-yl) acrylamide derivatives as TEAD proteins and inhibitors of the HIPPO-YAP1/TAZ signaling cascade for the treatment of cancer 赛诺菲 2023-01-31 — — CN disclosed
CN-105315262-A Benzpyrole-3-carboxylic acid benzimidazole-2-methyl ester derivative and synthetic method thereof UNIV QINGDAO SCIENCE & TECHNOLOGY 2016-02-10 — — CN disclosed
US-8232312-B2 Substituted arylsulphonylglycines, the preparation thereof and the use thereof as pharmaceutical compositions BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2012-07-31 — — US disclosed
US-8232312-B2 Substituted arylsulphonylglycines, the preparation thereof and the use thereof as pharmaceutical compositions BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2012-07-31 — — US disclosed
US-20120041207-A1 Compound STERIX LIMITED (GB) 2012-02-16 — — US disclosed
US-20110009448-A1 Compound STERIX LIMITED 2011-01-13 — — US disclosed
US-20100130557-A1 SUBSTITUTED ARYLSULPHONYLGLYCINES, THE PREPARATION THEREOF AND THE USE THEREOF AS PHARMACEUTICAL COMPOSITIONS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2010-05-27 — — US disclosed
US-20100130557-A1 SUBSTITUTED ARYLSULPHONYLGLYCINES, THE PREPARATION THEREOF AND THE USE THEREOF AS PHARMACEUTICAL COMPOSITIONS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2010-05-27 — — US disclosed
EP-2125718-A2 NEW SUBSTITUTED ARYLSULPHONYLGLYCINES, THE PREPARATION THEREOF AND THE USE THEREOF AS PHARMACEUTICAL COMPOSITIONS Boehringer Ingelheim International GmbH (DE) 2009-12-02 — — EP disclosed
WO-2008113760-A2 ARYLSULPHONYGLYCINE DERIVATIVES AS SUPPRESSORS OF THE INTERACTION OF GLYCOGEN PHOSPHORYLASE A WITH THE GL SUBUNIT OF GLYCOGEN-ASSOCIATED PROTEIN PHOSPHATASE 1 (PPL) FOR THE TREATMENT OF METABOLIC DISORDERS, PARTICULARY DIABETES BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2008-09-25 — — WO disclosed
US-20080114042-A1 Inhibiting 11 beta-hydroxysteroid dehydrogenase (11 beta-HSD); use of sulfonamide-substituted N-heterocyclics including pyrroles, oxazoles, thiazoles, imidazoles and their fused analogs to treat diabetes, obesity, hypertension, arthritis, asthma, osteoporosis, breast cancer STERIX LIMITED (GB) 2008-05-15 — — US disclosed
US-7309715-B2 Compound STERIX LIMITED (GB) 2007-12-18 — — US disclosed
WO-2007135380-A2 ANTIPARASITIC COMPOUNDS AND COMPOSITIONS MEDICAL RESEARCH COUNCIL (GB) 2007-11-29 — — WO disclosed
EP-1556040-A1 INHIBITORS OF 11-BETA-HYDROXY STEROID DEHYDROGENASE TYPE 1 AND TYPE 2 Sterix Limited (GB) 2005-07-27 — — EP disclosed
US-20040143124-A1 Compound STERIX LIMITED (GB) 2004-07-22 — — US disclosed
WO-2004037251-A1 INHIBITORS OF 11-BETA-HYDROXY STEROID DEHYDROGENASE TYPE 1 AND TYPE 2 STERIX LIMITED (GB) 2004-05-06 — — WO 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 (6 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-20080114042-A1 Inhibiting 11 beta-hydroxysteroid dehydrogenase (11 beta-HSD); use of sulfonamide-substituted N-heterocyclics including pyrroles, oxazoles, thiazoles, imidazoles and their fused analogs to treat diabetes, obesity, hypertension, arthritis, asthma, osteoporosis, breast cancer HSD11B1, HSD3B1, HSD11B2 NR4A2 169/4885GABRP 2459/4885GABRD 600/4885
US-20100130557-A1 SUBSTITUTED ARYLSULPHONYLGLYCINES, THE PREPARATION THEREOF AND THE USE THEREOF AS PHARMACEUTICAL COMPOSITIONS PYGL, PYGM, G6PC1 NR4A2 3961/4885GABRP 904/4885GABRD 2929/4885
US-20230140808-A1 (1 H-Indol-5-YL)Acrylamide Derivatives as Inhibitors of Tead Proteins and the Hippo-YAP1/TAZ Signaling Cascade for the Treatment of Cancer YAP1, YES1, TEAD1 NR4A2 3198/4885GABRP 3281/4885GABRD 3244/4885
US-20110009448-A1 Compound NR4A1, GPR6, PRMT6 NR4A2 21/4885GABRP 3686/4885GABRD 2412/4885
US-20120041207-A1 Compound NR4A1, GPR6, PRMT6 NR4A2 21/4885GABRP 3686/4885GABRD 2412/4885
US-20040143124-A1 Compound NR4A1, CBR1, NR2C2 NR4A2 26/4885GABRP 4007/4885GABRD 3377/4885

“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.

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