SCHEMBL974471

SCHEMBL974471

NNS(=O)(=O)NC(=O)c1ccccc1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 2/20 0.56
LMNA P02545 2/20 0.56
MEN1 O00255 1/20 0.56
CA12 O43570 2/20 0.56
CA1 P00915 2/20 0.56
CA9 Q16790 2/20 0.56
HDAC3 O15379 2/20 0.56
HDAC1 Q13547 2/20 0.56
HDAC2 Q92769 2/20 0.56
IDO1 P14902 1/20 0.56
ALOX15 P16050 1/20 0.56
HDAC7 Q8WUI4 1/20 0.56
HSD17B10 Q99714 1/20 0.56
HDAC8 Q9BY41 1/20 0.56
HDAC6 Q9UBN7 1/20 0.56
NCOR2 Q9Y618 1/20 0.56
FLT1 P17948 1/20 0.51
FLT4 P35916 1/20 0.51
KDR P35968 1/20 0.51
L3MBTL1 Q9Y468 1/20 0.51

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
SCHEMBL5819670 0.87 CA12 (0.65) KMT2ALMNAMEN1CA12CA1
SCHEMBL712594 0.81 CA1 (0.58) KMT2ALMNAMEN1CA12CA1
SCHEMBL11289818 0.79 HDAC3 (0.56) KMT2ALMNAMEN1CA12CA1
Bromide SCHEMBL7107771 0.79 KMT2A (0.56) KMT2ALMNAMEN1CA12CA1
SCHEMBL3729389 0.78 CA12 (0.60) KMT2ALMNAMEN1CA12CA1
SCHEMBL28046283 0.78 HDAC3 (0.54) KMT2ALMNAMEN1CA12CA1
SCHEMBL3053462 0.78 HDAC2 (0.54) KMT2ALMNAMEN1CA12CA1
SCHEMBL5372882 0.77 HDAC3 (0.58) KMT2ALMNAMEN1CA12CA1
SCHEMBL364110 0.77 HDAC3 (0.58) KMT2ALMNAMEN1CA12CA1
SCHEMBL1750909 0.77 CA12 (0.58) KMT2ALMNAMEN1CA12CA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8232421-B2 Bifunctional phenyl ISO (THIO) cyanates, processes and intermediates for their preparation BASF AKTIENGESELLSCHAFT (DE) 2012-07-31 US claimed
US-7820846-B2 by phosgenation of an aminobenzoylsulfamic acid amide intermediate; prepared from a p-nitrobenzoyl chloride or benzoate and a sulfamic acid amide and reducing the nitrobenzoylsulfamic acid amide; isocyanates are crop protection agents BASF AKTIENGESELLSCHAFT (DE) 2010-10-26 US claimed
CN-100368392-C Bifunctional phenyliso(thio)cyanates, processes and intermediates products for their preparation BASF AG (DE) 2008-02-13 CN claimed
US-20060004220-A1 Bifunctional phenyliso(thio)cyanates, processes and intermediates products for their Preparation BASF AKTIENGESELLSCHAFT (DE) 2006-01-05 US claimed
US-11219625-B2 Inhibitors of N-linked glycosylation and methods using same YALE UNIVERSITY (US) 2022-01-11 US disclosed
US-20190000858-A1 Inhibitors of N-Linked Glycosylation and Methods Using Same YALE UNIVERSITY 2019-01-03 US disclosed
WO-2017019540-A2 INHIBITORS OF N-LINKED GLYCOSYLATION AND METHODS USING SAME YALE UNIVERSITY (US) 2017-02-02 WO disclosed
US-8541611-B2 Bifunctional phenyl iso(thio)cyanates, processes and intermediates products for their preparation BASF AKTIENGESELLSCHAFT (DE) 2013-09-24 US disclosed
US-20120271049-A1 BIFUNCTIONAL PHENYL ISO (THIO) CYANATES, PROCESSES AND INTERMEDIATES PRODUCTS FOR THEIR PREPARATION BASF AKTIENGESELLSCHAFT (DE) 2012-10-25 US disclosed
US-8232421-B2 Bifunctional phenyl ISO (THIO) cyanates, processes and intermediates for their preparation BASF AKTIENGESELLSCHAFT (DE) 2012-07-31 US disclosed
US-20110009640-A1 BIFUNCTIONAL PHENYL ISO (THIO) CYANATES, PROCESSES AND INTERMEDIATES FOR THEIR PREPARATION BASF AKTIENGESELLSCHAFT (DE) 2011-01-13 US disclosed
US-7820846-B2 by phosgenation of an aminobenzoylsulfamic acid amide intermediate; prepared from a p-nitrobenzoyl chloride or benzoate and a sulfamic acid amide and reducing the nitrobenzoylsulfamic acid amide; isocyanates are crop protection agents BASF AKTIENGESELLSCHAFT (DE) 2010-10-26 US disclosed
CN-100368392-C Bifunctional phenyliso(thio)cyanates, processes and intermediates products for their preparation BASF AG (DE) 2008-02-13 CN disclosed
US-20060004220-A1 Bifunctional phenyliso(thio)cyanates, processes and intermediates products for their Preparation BASF AKTIENGESELLSCHAFT (DE) 2006-01-05 US disclosed
CN-1717388-A Bifunctional phenyliso(thio)cyanates, processes and intermediates products for their preparation BASF AG (DE) 2006-01-04 CN 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 (5 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-20190000858-A1 Inhibitors of N-Linked Glycosylation and Methods Using Same ENGASE, FUT5, B3GNT2 KMT2A 3565/4885LMNA 1668/4885MEN1 2573/4885
US-20120271049-A1 BIFUNCTIONAL PHENYL ISO (THIO) CYANATES, PROCESSES AND INTERMEDIATES PRODUCTS FOR THEIR PREPARATION TST, IDO1, TMT1A KMT2A 2541/4885LMNA 3604/4885MEN1 4685/4885
US-20110009640-A1 BIFUNCTIONAL PHENYL ISO (THIO) CYANATES, PROCESSES AND INTERMEDIATES FOR THEIR PREPARATION TST, IDO1, IDO2 KMT2A 2765/4885LMNA 3877/4885MEN1 4740/4885
US-11219625-B2 Inhibitors of N-linked glycosylation and methods using same ENGASE, FUT5, B3GNT2 KMT2A 3565/4885LMNA 1668/4885MEN1 2573/4885
US-20060004220-A1 Bifunctional phenyliso(thio)cyanates, processes and intermediates products for their Preparation TST, TMT1A, IDO1 KMT2A 2390/4885LMNA 3280/4885MEN1 4545/4885

“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.