Sulfadiazine

Sulfadiazine

SCHEMBL1486830

Cl.Cl.Nc1ccc(S(=O)(=O)Nc2ncccn2)cc1

nearest known ligand 0.96

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

folP

The experimentally established mechanism targets of Sulfadiazine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.96
AURKA O14965 1/20 0.96
DHFR P00374 1/20 0.96
TSHR P16473 1/20 0.96
SMN1; SMN2 Q16637 2/20 0.66
CYP2C9 P11712 2/20 0.65
MAPT P10636 2/20 0.65
ALDH1A1 P00352 4/20 0.59
TDP1 Q9NUW8 3/20 0.57
KMT2A Q03164 3/20 0.57
MEN1 O00255 1/20 0.57
CYP3A4 P08684 1/20 0.57
L3MBTL1 Q9Y468 3/20 0.56
PRMT1 Q99873 1/20 0.56
KDM4E B2RXH2 2/20 0.55
EDNRA P25101 1/20 0.55
SLC6A4 P31645 1/20 0.55
ADRA1A P35348 1/20 0.55
PRMT6 Q96LA8 1/20 0.55

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
Sulfadiazine SCHEMBL11611850 1.00 LMNA (0.96) LMNAAURKADHFRTSHRSMN1; SMN2
Sulfadiazine SCHEMBL1486826 1.00 LMNA (0.96) LMNAAURKADHFRTSHRSMN1; SMN2
Sulfadiazine SCHEMBL24176 0.98 LMNA (1.00) LMNAAURKADHFRTSHRSMN1; SMN2
Sulfadiazine SCHEMBL10422849 0.98 LMNA (1.00) LMNAAURKADHFRTSHRSMN1; SMN2
Sulfadiazine SCHEMBL30080807 0.98 LMNA (1.00) LMNAAURKADHFRTSHRSMN1; SMN2
Sulfadiazine SCHEMBL6141086 0.96 LMNA (0.96) LMNAAURKADHFRTSHRSMN1; SMN2
Sulfadiazine SCHEMBL16860643 0.96 LMNA (0.96) LMNAAURKADHFRTSHRSMN1; SMN2
Sulfadiazine SCHEMBL34517 0.96 LMNA (0.96) LMNAAURKADHFRTSHRSMN1; SMN2
Sulfadiazine SCHEMBL3728176 0.96 LMNA (0.96) LMNAAURKADHFRTSHRSMN1; SMN2
Sulfadiazine SCHEMBL5870705 0.96 LMNA (0.96) LMNAAURKADHFRTSHRSMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8703116-B2 Modified macromolecule STARPHARMA PTY LIMITED (AU) 2014-04-22 US disclosed
US-8445528-B2 Dendrimer conjugates THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2013-05-21 US disclosed
US-20130116432-A1 MODIFIED MACROMOLECULE STARPHARMA PTY LTD (AU) 2013-05-09 US disclosed
US-8337823-B2 Modified macromolecule STARPHARMA PTY LIMITED (AU) 2012-12-25 US disclosed
US-20120277376-A1 DENDRIMER CONJUGATES THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2012-11-01 US disclosed
US-8252834-B2 Dendrimer conjugates THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2012-08-28 US disclosed
US-8163805-B2 Small molecule antagonists of Bcl-2 family proteins THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2012-04-24 US disclosed
US-7910621-B2 Small molecule antagonists of XIAP family proteins THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2011-03-22 US disclosed
EP-1474121-B1 Synergistic association of (-)- gossypol with docetaxel or paclitaxel for cancer treatment UNIV MICHIGAN (US) 2010-07-21 EP disclosed
US-20100069344-A1 SMALL MOLECULE ANTAGONISTS OF BCL2 FAMILY PROTEINS THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2010-03-18 US disclosed
EP-1474121-A2 SMALL MOLECULE ANTAGONISTS OF BCL2 FAMILY PROTEINS THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2004-11-10 EP disclosed
US-20040214902-A1 Small molecule antagonists of BCL-2 family proteins THE REGENTS OF THE UNIVERSITY OF MICHIGAN 2004-10-28 US disclosed
US-20030199489-A1 Small molecule inhibitors targeted at BCL-2 THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2003-10-23 US disclosed
WO-2003038060-A2 SMALL MOLECULE INHIBITORS TARGETED AT BCL-2 THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2003-05-08 WO disclosed
EP-1301211-A2 MULTIFUNCTIONAL NANODEVICE PLATFORM THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2003-04-16 EP disclosed
US-20030008924-A1 Small molecule antagonists of Bcl-2 family proteins THE REGENTS OF THE UNIVERSITY OF MICHIGAN 2003-01-09 US disclosed
WO-2002097053-A2 SMALL MOLECULE ANTAGONISTS OF BCL2 FAMILY PROTEINS THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2002-12-05 WO disclosed
US-20020165179-A1 Multifunctional nanodevice platform NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR 2002-11-07 US disclosed
US-6471968-B1 DENDRIMER BASED MULTIFUNCTIONAL COMPOSITIONS FOR DISEASE DIAGNOSIS AND THERAPY (E.G. CANCER DIAGNOSIS AND THERAPY); FIRST DENDRIMER IS A POLYAMIDOAMINE (PAMAM) DENDRIMER, SECOND DENDRIMER IS A POLYPROPYLAMINE (POPAM) DENDRIMER REGENTS OF THE UNIVERSITY OF MICHIGAN 2002-10-29 US disclosed
WO-2001087348-A2 MULTIFUNCTIONAL NANODEVICE PLATFORM THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2001-11-22 WO 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 (3 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-20040214902-A1 Small molecule antagonists of BCL-2 family proteins BCL2L1, BCL2, BCL2L2 LMNA 1912/4885AURKA 4403/4885DHFR 1387/4885
US-20100069344-A1 SMALL MOLECULE ANTAGONISTS OF BCL2 FAMILY PROTEINS BCL2L1, BCL2, BCL2L11 LMNA 2064/4885AURKA 4262/4885DHFR 1523/4885
US-20030199489-A1 Small molecule inhibitors targeted at BCL-2 BCL2L1, BCL2, BCL2L2 LMNA 3640/4885AURKA 2479/4885DHFR 1580/4885

“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.