SCHEMBL5567709

SCHEMBL5567709

Nc1cccc(C(=O)Nc2cc(S(=O)(=O)O)cc3cc(S(=O)(=O)O)cc(O)c23)c1

nearest known ligand 0.76

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
APEX1 P27695 1/20 0.76
CASP6 P55212 2/20 0.49
CTDSP1 Q9GZU7 1/20 0.49
HDAC1 Q13547 1/20 0.49
HSD17B10 Q99714 3/20 0.49
SMN1; SMN2 Q16637 1/20 0.49
NPSR1 Q6W5P4 1/20 0.49
NT5E P21589 2/20 0.48
ENPP2 Q13822 2/20 0.46
ALDH1A1 P00352 3/20 0.46
TDP1 Q9NUW8 2/20 0.46
TSHR P16473 1/20 0.46
KDM4C Q9H3R0 1/20 0.45
NSD2 O96028 1/20 0.45
DUSP3 P51452 1/20 0.45
PTPN5 P54829 1/20 0.45
PTPN11 Q06124 1/20 0.45
KAT6A Q92794 1/20 0.45
MEN1 O00255 2/20 0.44
KMT2A Q03164 2/20 0.44

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
SCHEMBL11440872 0.92 APEX1 (0.63) APEX1CASP6CTDSP1HDAC1HSD17B10
SCHEMBL11426178 0.92 APEX1 (0.63) APEX1CASP6CTDSP1HDAC1HSD17B10
SCHEMBL11472832 0.88 APEX1 (0.58) APEX1CASP6CTDSP1HDAC1HSD17B10
SCHEMBL10876642 0.87 APEX1 (0.77) APEX1NPSR1ENPP2ALDH1A1KAT6A
SCHEMBL11593854 0.87 APEX1 (0.81) APEX1CASP6CTDSP1HSD17B10NT5E
SCHEMBL6560534 0.86 APEX1 (0.77) APEX1CASP6CTDSP1HDAC1NT5E
SCHEMBL11589917 0.86 APEX1 (0.77) APEX1CASP6CTDSP1HDAC1NT5E
SCHEMBL9411865 0.86 APEX1 (1.00) APEX1CASP6CTDSP1HDAC1HSD17B10
SCHEMBL1413131 0.86 APEX1 (1.00) APEX1CASP6CTDSP1HDAC1HSD17B10
SCHEMBL10944877 0.86 APEX1 (0.76) APEX1SMN1; SMN2ENPP2ALDH1A1TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4103028-A SUBSTITUTED HYDROXY NAPHTHALENEDISULFONIC ACIDS AMERICAN CYANAMID COMPANY (US) 1978-07-25 US claimed
US-20070151479-A1 Acidic monoazo dyestuffs CLARIANT FINANCE (BVI) LIMITED (VG) 2007-07-05 US disclosed
EP-1704187-A1 ACIDIC MONOAZO DYESTUFFS CLARIANT INTERNATIONAL LTD. (CH) 2006-09-27 EP disclosed
WO-2005073323-A1 ACIDIC MONOAZO DYESTUFFS CLARIANT INTERNATIONAL LTD (CH) 2005-08-11 WO disclosed
EP-1055710-B1 Water-soluble fibre-reactive dyestuffs, process for their preparation and their use DYSTAR TEXTILFARBEN GMBH & CO (DE) 2004-08-11 EP disclosed
US-6444794-B1 COMPLEXING WITH SUBSTRATE DYSTAR TEXTILFARBEN GMBH & CO. DEUTSCHLAND KG (DE) 2002-09-03 US disclosed
EP-1055710-A1 Water-soluble fibre-reactive dyestuffs, process for their preparation and their use DyStar Textilfarben GmbH & Co. Deutschland KG (DE) 2000-11-29 EP disclosed
EP-0542079-B1 Process for continuously reacting halogenopyrimidines with amines BAYER AG (DE) 1997-07-23 EP disclosed
EP-0548795-B1 Water-soluble reactive dyes, their manufacture and their use HOECHST AG (DE) 1997-07-09 EP disclosed
US-5578712-A Fibre-reactive monoazonaphthyl dyestuffs SANDOZ LTD. (CH) 1996-11-26 US disclosed
US-5091515-A PROCESS FOR THE PREPARATION OF SUBSTITUTED 2,4-DIAMINO-6-FLUORO-S-TRIAZINES BAYER AKTIENGESELLSCHAFT (DE) 1992-02-25 US disclosed
WO-1991009914-A1 AZO COMPOUNDS, PROCESS FOR PRODUCING THEM AND THEIR USE AS COLORANTS HOECHST AKTIENGESELLSCHAFT (DE) 1991-07-11 WO disclosed
WO-1990013603-A1 WATER-SOLUBLE AZO DYES, PROCESS FOR PRODUCING THEM AND THEIR USE HOECHST AKTIENGESELLSCHAFT (DE) 1990-11-15 WO disclosed
US-4929719-A Fiber-reactive dyes containing an aniline radical which carries two different vinylsulfonyl moieties CIBA-GEIGY CORPORATION (US) 1990-05-29 US disclosed
US-4875903-A PRINTING,DYEING SANDOZ LTD. (CH) 1989-10-24 US disclosed
US-4391824-A INHIBITING CONNECTIVE TISSUE DISTRUCTION, ENZYME INHIBITORS AMERICAN CYANAMID COMPANY (US) 1983-07-05 US disclosed
EP-0024668-B1 REACTIVE DYESTUFFS AND THEIR USE IN DYEING AND PRINTING HYDROXYL GROUPS AND NITROGEN CONTAINING MATERIALS BAYER AG (DE) 1983-04-13 EP disclosed
US-4103028-A SUBSTITUTED HYDROXY NAPHTHALENEDISULFONIC ACIDS AMERICAN CYANAMID COMPANY (US) 1978-07-25 US disclosed
US-4054559-A Reactive disazo monohalogenotriazine dyestuffs NIPPON KAYAKU KABUSHIKI KAISHA (JA) 1977-10-18 US disclosed
US-4046805-A Substituted-hydroxy-naphthalenedisulfonic acid compounds AMERICAN CYANAMID COMPANY (US) 1977-09-06 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 (1 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-20070151479-A1 Acidic monoazo dyestuffs PAH, TYR, CD68 APEX1 2834/4885CASP6 4675/4885CTDSP1 4084/4885

“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.