SCHEMBL8592778

SCHEMBL8592778

CC(=O)Nc1ccc(N)c2cc(S(=O)(=O)O)ccc12

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CASP6 P55212 2/20 0.60
▸ NPC1 O15118 1/20 0.51
▸ CA1 P00915 7/20 0.48
▸ CA2 P00918 7/20 0.48
▸ CA9 Q16790 5/20 0.48
▸ KMT2A Q03164 1/20 0.46
▸ PHLPP2 Q6ZVD8 1/20 0.45
▸ HSD17B10 Q99714 3/20 0.44
▸ ALDH1A1 P00352 3/20 0.44
▸ CYP2C19 P33261 3/20 0.44
▸ CYP2C9 P11712 2/20 0.44
▸ KDM4E B2RXH2 1/20 0.43
▸ MAPT P10636 1/20 0.43
▸ HPGD P15428 1/20 0.43
▸ HDAC3 O15379 1/20 0.41
▸ HDAC1 Q13547 1/20 0.41
▸ HDAC2 Q92769 1/20 0.41
▸ RXFP1 Q9HBX9 1/20 0.41
▸ PKM P14618 1/20 0.40
▸ CA12 O43570 2/20 0.40

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
SCHEMBL10960119 0.94 CASP6 (0.60) CASP6NPC1CA1CA2CA9
SCHEMBL3301802 0.84 CASP6 (0.66) CASP6NPC1CA1CA2CA9
SCHEMBL8592933 0.83 NPC1 (0.70) CASP6NPC1CA1CA2CA9
SCHEMBL11813062 0.80 CASP6 (0.53) CASP6NPC1CA1CA2CA9
SCHEMBL6051371 0.79 ALDH1A1 (0.59) CASP6CA1CA2KMT2APHLPP2
SCHEMBL11355099 0.78 NPC1 (0.48) CASP6NPC1CA1CA2CA9
SCHEMBL12177955 0.76 HSD17B10 (0.43) CASP6PHLPP2HSD17B10ALDH1A1CYP2C19
SCHEMBL24280284 0.76 PHLPP2 (0.67) NPC1PHLPP2HSD17B10CYP2C19CYP2C9
SCHEMBL14413297 0.76 PHLPP2 (0.67) NPC1PHLPP2HSD17B10CYP2C19CYP2C9
SCHEMBL11435627 0.76 ALDH1A1 (0.42) CASP6CA1CA2CA9KMT2A

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 13 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0555699-B1 Process for the preparation of aminourethanes BAYER AG (DE) 1998-01-07 — — EP disclosed
US-4540776-A Reactive fluorotriazinylaminonaphthotriazolyphenylazopyridone or pyrimidone dyestuffs BAYER AKTIENGESELLSCHAFT (DE) 1985-09-10 — — US disclosed
US-4354968-A Azo reactive dyestuffs having an aryl-triazinyl-aryl diazo component BAYER AKTIENGESELLSCHAFT (DE) 1982-10-19 — — US disclosed
EP-0013879-B1 REACTIVE DYESTUFFS, THEIR PREPARATION AND THEIR USE FOR DYEING MATERIALS CONTAINING HYDROXYL OR AMIDE GROUPS BAYER AG (DE) 1982-09-15 — — EP disclosed
EP-0038453-A2 Process for the preparation of water soluble phthalocyanine dyestuffs BAYER AG (DE) 1981-10-28 — — EP disclosed
US-4268267-A PRINTING AND DYEING TEXTILES BAYER AKTIENGESELLSCHAFT (DE) 1981-05-19 — — US disclosed
US-4129736-A FIBER-REACTIVE CIBA-GEIGY CORPORATION (US) 1978-12-12 — — US disclosed
US-4118384-A DIAZOTIZATION BAYER AKTIENGESELLSCHAFT (DE) 1978-10-03 — — US disclosed
US-4082739-A FIBRE-REACTIVE DYESTUFF CONTAINING A BIS-TRIAZINYLAMINO CIBA-GEIGY AG (CH) 1978-04-04 — — US disclosed
US-4079051-A 4-Halogeno-s-triazin-2-yl-phosphoramide acid containing reactive dyestuffs CIBA-GEIGY CORPORATION (US) 1978-03-14 — — US disclosed
US-4035350-A Process for the preparation of water-soluble azo dyestuffs by reacting an aromatic amine and a coupling component with alkali metal nitrite or alkyl nitrite in the absence of acid HOECHST AKTIENGESELLSCHAFT (DT) 1977-07-12 — — US disclosed
US-4033944-A Fibre-reactive hydroxycycloalkenyl-halo triazinyl containing dyestuffs CIBA-GEIGY CORPORATION (US) 1977-07-05 — — US disclosed
US-3947407-A ANTHRAQUINONE DYE CIBA-GEIGY AG (CH) 1976-03-30 — — US disclosed
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