SCHEMBL97957

SCHEMBL97957

COc1ccc(CBr)cc1[N+](=O)[O-]

nearest known ligand 0.66

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.66
ALDH1A1 P00352 13/20 0.57
LMNA P02545 3/20 0.57
HTT P42858 3/20 0.57
GAA P10253 1/20 0.57
PKM P14618 1/20 0.54
TDP1 Q9NUW8 1/20 0.51
GFER P55789 1/20 0.51
CYP1A2 P05177 1/20 0.51
CYP2C19 P33261 1/20 0.51
MEN1 O00255 2/20 0.50
KMT2A Q03164 2/20 0.50
TTR P02766 1/20 0.50

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
SCHEMBL3720228 0.87 SMN1; SMN2 (0.59) SMN1; SMN2ALDH1A1LMNAHTTGAA
SCHEMBL29788546 0.87 ALDH1A1 (0.51) SMN1; SMN2ALDH1A1LMNAHTTGAA
SCHEMBL520427 0.87 ALDH1A1 (0.51) SMN1; SMN2ALDH1A1LMNAHTTGAA
SCHEMBL31090163 0.86 SMN1; SMN2 (0.61) SMN1; SMN2ALDH1A1LMNAHTTGAA
SCHEMBL16233087 0.86 SMN1; SMN2 (0.61) SMN1; SMN2ALDH1A1LMNAHTTGAA
SCHEMBL8297975 0.85 ALDH1A1 (0.61) SMN1; SMN2ALDH1A1LMNAHTTGAA
SCHEMBL28712446 0.85 SMN1; SMN2 (0.59) SMN1; SMN2ALDH1A1LMNAHTTGAA
SCHEMBL6489059 0.84 SMN1; SMN2 (0.50) SMN1; SMN2ALDH1A1LMNAHTTGAA
SCHEMBL4512978 0.84 SMN1; SMN2 (0.67) SMN1; SMN2ALDH1A1LMNAHTTGAA
SCHEMBL1667910 0.83 TTR (0.68) SMN1; SMN2ALDH1A1LMNAHTTGAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4692096-A1 MACROCYCLIC COMPOUND, AND PHARMACEUTICAL COMPOSITION AND USE THEREOF Prime Gene Therapeutics Co., Ltd. (CN) 2026-02-11 EP disclosed
US-12479834-B2 Phenol compound or salt thereof TAIHO PHARMACEUTICAL CO., LTD. (JP) 2025-11-25 US disclosed
US-20250276977-A1 TYK2 INHIBITORS AND USES THEREOF ALUMIS INC (US) 2025-09-04 US disclosed
CN-119977833-A Synthesis and antitumor application of erianin derivative 江苏海洋大学 2025-05-13 CN disclosed
US-12145927-B2 Inhibitors of indoleamine 2,3-dioxygenase and methods of their use BRISTOL-MYERS SQUIBB COMPANY (US) 2024-11-19 US disclosed
CN-113811534-B TYK2 inhibitors and uses thereof 阿鲁米斯公司 2024-10-29 CN disclosed
WO-2024199479-A1 MACROCYCLIC COMPOUND, AND PHARMACEUTICAL COMPOSITION AND USE THEREOF 北京普祺医药科技股份有限公司 2024-10-03 WO disclosed
CN-114591351-B Polycyclic compound and preparation method and application thereof 成都科岭源医药技术有限公司 2023-12-05 CN disclosed
US-20230049402-A1 NOVEL PHENOL COMPOUND OR SALT THEREOF TAIHO PHARMACEUTICAL CO. LTD. (JP) 2023-02-16 US disclosed
EP-4067343-A1 NOVEL PHENOL COMPOUND OR SALT THEREOF Taiho Pharmaceutical Co., Ltd. (JP) 2022-10-05 EP disclosed
US-20030220404-A1 Process for the preparation of combretastatins AVENTIS PHARMA S.A. (FR) 2003-11-27 US disclosed
US-20030187068-A1 Substituted phenylpropionic acid derivatives KYORIN PHARMACEUTICAL CO., LTD. (JP) 2003-10-02 US disclosed
WO-2003072062-A2 AMINO-SUBSTITUTED (E)-2,6-DIALKOXYSTYRYL 4-SUBSTITUTED BENZYLSULFONES FOR TREATING PROLIFERATIVE DISORDERS TEMPLE UNIVERSITY-OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION (US) 2003-09-04 WO disclosed
US-6582351-B1 Benzimidazole heterocyclic compounds having pharmacological activities, and their use as a medicament for treatment or prevention of diseases mediated by cGMP-PDE FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2003-06-24 US disclosed
EP-1285908-A1 SUBSTITUTED PHENYLPROPIONIC ACID DERIVATIVES KYORIN PHARMACEUTICAL CO., LTD. (JP) 2003-02-26 EP disclosed
EP-1196391-A1 BENZIMIDAZOLONE DERIVATIVES AND THEIR USE AS PHOSPHODIESTERASE INHIBITORS FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2002-04-17 EP disclosed
WO-2001005770-A1 BENZIMIDAZOLONE DERIVATIVES AND THEIR USE AS PHOSPHODIESTERASE INHIBITORS FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2001-01-25 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
US-5952362-A INHIBITOR OF GLYCOGEN PHOSPHORYLASE ENZYMETIC ACTIVITY AND GLUCOSE ACITIVITY SYNTEX (U.S.A) INC. (US) 1999-09-14 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 (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-20250276977-A1 TYK2 INHIBITORS AND USES THEREOF TYK2, JAK1, JAK2 SMN1; SMN2 1274/4885ALDH1A1 4098/4885LMNA 3948/4885
US-20030187068-A1 Substituted phenylpropionic acid derivatives PPARA, PPARG, PPARD SMN1; SMN2 4657/4885ALDH1A1 429/4885LMNA 2358/4885
US-20030220404-A1 Process for the preparation of combretastatins TGFB2, HMGCR, TGFB1 SMN1; SMN2 1402/4885ALDH1A1 2753/4885LMNA 277/4885
US-12145927-B2 Inhibitors of indoleamine 2,3-dioxygenase and methods of their use IDO1, IDO2, INMT SMN1; SMN2 4581/4885ALDH1A1 508/4885LMNA 4684/4885
US-12479834-B2 Phenol compound or salt thereof REN, MLX, MYB SMN1; SMN2 3261/4885ALDH1A1 287/4885LMNA 1482/4885
US-20230049402-A1 NOVEL PHENOL COMPOUND OR SALT THEREOF MYB, MLX, EP300 SMN1; SMN2 3158/4885ALDH1A1 235/4885LMNA 2792/4885

“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.