SCHEMBL528040

SCHEMBL528040

CC(C)Oc1cc(C(=O)O)ccc1[N+](=O)[O-]

nearest known ligand 0.61

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
EP300 Q09472 1/20 0.61
HIF1A Q16665 1/20 0.61
CASP6 P55212 1/20 0.58
TSHR P16473 2/20 0.58
PDK1 Q15118 1/20 0.57
MYC P01106 2/20 0.55
MAX P61244 2/20 0.55
HCAR3 P49019 7/20 0.54
LMNA P02545 1/20 0.50
TTR P02766 1/20 0.50
KMT2A Q03164 2/20 0.47
MEN1 O00255 1/20 0.47

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
SCHEMBL30658490 1.00 EP300 (0.61) EP300HIF1ACASP6TSHRPDK1
SCHEMBL2550259 0.88 PDK1 (0.72) EP300HIF1ACASP6TSHRPDK1
SCHEMBL527425 0.86 HCAR3 (0.55) EP300HIF1ACASP6TSHRMYC
SCHEMBL28107004 0.86 MAPK1 (0.58) EP300HIF1ATSHRPDK1MYC
SCHEMBL1560385 0.85 AR (0.58) EP300HIF1APDK1MYCMAX
SCHEMBL17775445 0.85 PDK1 (0.54) EP300HIF1ACASP6TSHRPDK1
SCHEMBL16392507 0.85 PDK1 (0.54) EP300HIF1ATSHRPDK1MYC
SCHEMBL16974724 0.85 CASP6 (0.63) EP300HIF1ACASP6TSHRMYC
SCHEMBL31003858 0.85 CASP6 (0.63) EP300HIF1ACASP6TSHRMYC
SCHEMBL223878 0.83 TTR (0.64) CASP6TSHRMYCMAXHCAR3

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
US-20260014260-A1 MDM2 DEGRADER NEWAVE PHARMACEUTICAL INC (US) 2026-01-15 US disclosed
WO-2023230059-A1 MDM2 DEGRADER NEWAVE PHARMACEUTICAL INC. (US) 2023-11-30 WO disclosed
CN-110997627-B Cyst amide derivatives 亥姆霍兹感染研究中心有限公司 2023-10-10 CN disclosed
US-11034648-B2 Cystobactamide derivatives HELMHOLTZ-ZENTRUM FÜR (DE) 2021-06-15 US disclosed
US-11034648-B2 Cystobactamide derivatives HELMHOLTZ-ZENTRUM FÜR (DE) 2021-06-15 US disclosed
EP-3672937-A1 NOVEL CYSTOBACTAMIDE DERIVATIVES Helmholtz-Zentrum für Infektionsforschung GmbH (DE) 2020-07-01 EP disclosed
US-20200190020-A1 NOVEL CYSTOBACTAMIDE DERIVATIVES Helmholtz-Zentrum für Infektionsforschung GmbH (DE) 2020-06-18 US disclosed
US-20200190020-A1 NOVEL CYSTOBACTAMIDE DERIVATIVES Helmholtz-Zentrum für Infektionsforschung GmbH (DE) 2020-06-18 US disclosed
CN-110997627-A Novel cystobacter amide derivatives 亥姆霍兹感染研究中心有限公司 2020-04-10 CN disclosed
WO-2019038405-A1 NOVEL CYSTOBACTAMIDE DERIVATIVES Helmholtz-Zentrum für Infektionsforschung GmbH (DE) 2019-02-28 WO disclosed
EP-2598161-A2 GLP-1 RECEPTOR AGONIST COMPOUNDS HAVING STABILIZED REGIONS Amylin Pharmaceuticals, LLC (US) 2013-06-05 EP disclosed
WO-2012015975-A2 GLP-1 RECEPTOR AGONIST COMPOUNDS HAVING STABILIZED REGIONS AMYLIN PHARMACEUTICALS, INC. (US) 2012-02-02 WO disclosed
WO-2012015975-A2 GLP-1 RECEPTOR AGONIST COMPOUNDS HAVING STABILIZED REGIONS AMYLIN PHARMACEUTICALS, INC. (US) 2012-02-02 WO disclosed
US-8003785-B2 Halo-substituted pyrimidodiazepines TAKEDA PHARMACEUTICAL COMPANY LIMITED (US) 2011-08-23 US disclosed
EP-2303889-A1 HALO-SUBSTITUTED PYRIMIDODIAZEPINES AS PLKL INHIBITORS F. Hoffmann-La Roche AG (CH) 2011-04-06 EP disclosed
US-20090318408-A1 HALO-SUBSTITUTED PYRIMIDODIAZEPINES TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2009-12-24 US disclosed
WO-2009153197-A1 HALO-SUBSTITUTED PYRIMIDODIAZEPINES AS PLKL INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2009-12-23 WO disclosed
EP-1217434-A2 Silver halide photographic element EASTMAN KODAK COMPANY (US) 2002-06-26 EP disclosed
EP-1217435-A1 Silver halide photographic element and imaging process EASTMAN KODAK COMPANY (US) 2002-06-26 EP disclosed
US-6361931-B1 REACTIVITY, STABILITY EASTMAN KODAK COMPANY 2002-03-26 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 (4 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-11034648-B2 Cystobactamide derivatives CTH, CBS, SLC7A11 EP300 3960/4885HIF1A 1589/4885CASP6 1077/4885
US-20260014260-A1 MDM2 DEGRADER MDM2, TP53, ADRM1 EP300 4085/4885HIF1A 3690/4885CASP6 1328/4885
US-20200190020-A1 NOVEL CYSTOBACTAMIDE DERIVATIVES CTH, CBS, SLC7A11 EP300 4224/4885HIF1A 1978/4885CASP6 1090/4885
US-20090318408-A1 HALO-SUBSTITUTED PYRIMIDODIAZEPINES PLK1, CCNI, CDK1 EP300 472/4885HIF1A 4196/4885CASP6 3565/4885

“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.