SCHEMBL710379

SCHEMBL710379

CN[C@H]1CN(c2ccc3c(=O)c(C(=O)O)cn(-c4nccs4)c3n2)C[C@@H]1O

nearest known ligand 0.37

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR3A P46098 3/20 0.37
LMNA P02545 3/20 0.35
KMT2A Q03164 3/20 0.35
MEN1 O00255 1/20 0.35
ABCC4 O15439 1/20 0.35
PKM P14618 1/20 0.35
PTGS1 P23219 1/20 0.35
CHRNA7 P36544 3/20 0.34
TSHR P16473 1/20 0.34
HIF1A Q16665 1/20 0.34
ALDH1A1 P00352 2/20 0.33
HSD17B10 Q99714 2/20 0.33
KDM4E B2RXH2 1/20 0.33
POLB P06746 1/20 0.33
HPGD P15428 1/20 0.33
XBP1 P17861 1/20 0.33
NFKB1 P19838 1/20 0.33
HTT P42858 1/20 0.33
NFKB2 Q00653 1/20 0.33
RELA Q04206 1/20 0.33

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
SCHEMBL15580366 0.91 HTR3A (0.37) HTR3ALMNAKMT2AMEN1ABCC4
Vosaroxin SCHEMBL674441 0.89 HTR3A (0.35) HTR3ALMNAKMT2AMEN1ABCC4
Vosaroxin SCHEMBL15933161 0.89 HTR3A (0.35) HTR3ALMNAKMT2AMEN1ABCC4
Vosaroxin SCHEMBL195037 0.89 HTR3A (0.35) HTR3ALMNAKMT2AMEN1ABCC4
Vosaroxin SCHEMBL3207291 0.89 HTR3A (0.35) HTR3ALMNAKMT2AMEN1ABCC4
SCHEMBL12055755 0.89 HTR3A (0.35) HTR3ALMNAKMT2AMEN1ABCC4
SCHEMBL13212356 0.88 CHRNA7 (0.34) HTR3AKMT2AMEN1CHRNA7ALDH1A1
Vosaroxin SCHEMBL7824841 0.88 HTR3A (0.35) HTR3ALMNAKMT2AMEN1ABCC4
Hydrochloric Acid SCHEMBL7835838 0.88 HTR3A (0.38) HTR3ALMNAKMT2AMEN1ABCC4
Vosaroxin SCHEMBL7824869 0.88 HTR3A (0.35) HTR3ALMNAKMT2AMEN1ABCC4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100203162-A1 Method of preparing (+)-1,4-dihydro-7-[(3S,4S)-3-methoxy-4-(methylamino)-1-pyrrolidinyl]-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3-carboxylic acid SUNESIS PHARMACEUTICALS, INC. 2010-08-12 US claimed
EP-3287126-A1 METHODS OF USING SNS-595 FOR TREATMENT OF CANCER SUBJECTS WITH REDUCED BRCA2 ACTIVITY Sunesis Pharmaceuticals, Inc. (US) 2018-02-28 EP disclosed
EP-3284745-A1 COMPOSITION OF (+)-1,4-DIHYDRO-7-[(3S,4S)-3-METHOXY-4-(METHYLAMINO)-1-PYRROLIDINYL]-4-OXO-1-(2-THIAZOLYL)-1,8-NAPHTHYRIDINE-3-CARBOXYLIC ACID Sunesis Pharmaceuticals, Inc. (US) 2018-02-21 EP disclosed
EP-3284745-A1 COMPOSITION OF (+)-1,4-DIHYDRO-7-[(3S,4S)-3-METHOXY-4-(METHYLAMINO)-1-PYRROLIDINYL]-4-OXO-1-(2-THIAZOLYL)-1,8-NAPHTHYRIDINE-3-CARBOXYLIC ACID Sunesis Pharmaceuticals, Inc. (US) 2018-02-21 EP disclosed
US-9839630-B2 Method of preparing (+)-1,4-dihydro-7-[(3S,4S)-3-methoxy-4-(methylamino)-1-pyrrolidinyl]-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3-carboxylic acid SUNESIS PHARMACEUTICALS, INC. (US) 2017-12-12 US disclosed
US-9839630-B2 Method of preparing (+)-1,4-dihydro-7-[(3S,4S)-3-methoxy-4-(methylamino)-1-pyrrolidinyl]-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3-carboxylic acid SUNESIS PHARMACEUTICALS, INC. (US) 2017-12-12 US disclosed
EP-2382214-B1 METHOD OF PREPARING (+)-1,4-DIHYDRO-7-[(3S,4S)-3-METHOXY-4-(METHYLAMINO)-1-PYRROLIDINYL]-4-OXO-1-(2-THIAZOLYL)-1,8-NAPHTHYRIDINE-3-CARBOXYLIC ACID SUNESIS PHARMACEUTICALS INC (US) 2017-07-19 EP disclosed
EP-2382214-B1 METHOD OF PREPARING (+)-1,4-DIHYDRO-7-[(3S,4S)-3-METHOXY-4-(METHYLAMINO)-1-PYRROLIDINYL]-4-OXO-1-(2-THIAZOLYL)-1,8-NAPHTHYRIDINE-3-CARBOXYLIC ACID SUNESIS PHARMACEUTICALS INC (US) 2017-07-19 EP disclosed
US-20170182015-A1 METHODS OF USING SNS-595 FOR TREATMENT OF CANCER SUBJECTS WITH REDUCED BRCA2 ACTIVITY SUNESIS PHARMACEUTICALS INC (US) 2017-06-29 US disclosed
US-9676774-B2 Compounds and compositions for treatment of cancer SUNESIS PHARMACEUTICALS, INC. (US) 2017-06-13 US disclosed
US-20120148564-A1 METHODS OF USING SNS-595 FOR TREATMENT OF CANCER SUBJECTS WITH REDUCED BRCA2 ACTIVITY SUNESIS PHARMACEUTICALS, INC. 2012-06-14 US disclosed
US-8124773-B2 1,8-naphthyridine compounds for the treatment of cancer SUNESIS PHARMACEUTICALS, INC. (US) 2012-02-28 US disclosed
EP-2382214-A1 METHOD OF PREPARING (+)-1,4-DIHYDRO-7-Ý(3S,4S)-3METHOXY-4-(METHYLAMINO)-1-PYRROLIDINYL¨-4-OXO-1-(2-THIAZOLYL)-1,8-NAPHTHYRIDINE-3-CARBOXYLIC ACID Sunesis Pharmaceuticals, Inc. (US) 2011-11-02 EP disclosed
EP-2354138-A1 Compounds and compositions for treatment of cancer Sunesis Pharmaceuticals, Inc. (US) 2011-08-10 EP disclosed
US-20100203162-A1 Method of preparing (+)-1,4-dihydro-7-[(3S,4S)-3-methoxy-4-(methylamino)-1-pyrrolidinyl]-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3-carboxylic acid SUNESIS PHARMACEUTICALS, INC. 2010-08-12 US disclosed
WO-2010078294-A1 METHOD OF PREPARING (+)-1,4-DIHYDRO-7-[(3S,4S)-3METHOXY-4-(METHYLAMINO)-1-PYRROLIDINYL]-4-OXO-1-(2-THIAZOLYL)-1,8-NAPHTHYRIDINE-3-CARBOXYLIC ACID SUNESIS PHARMACEUTICAL, INC. (US) 2010-07-08 WO disclosed
US-20100029708-A1 COMPOUNDS AND COMPOSITIONS FOR TREATMENT OF CANCER SUNESIS PHARMACEUTICALS, INC. 2010-02-04 US disclosed
EP-2043645-A2 COMPOUNDS AND COMPOSITIONS FOR TREATMENT OF CANCER Sunesis Pharmaceuticals, Inc. (US) 2009-04-08 EP disclosed
WO-2007146335-A2 COMPOUNDS AND COMPOSITIONS FOR TREATMENT OF CANCER SUNESIS PHARMACEUTICALS, INC. (US) 2007-12-21 WO disclosed
WO-2007146335-A2 COMPOUNDS AND COMPOSITIONS FOR TREATMENT OF CANCER SUNESIS PHARMACEUTICALS, INC. (US) 2007-12-21 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 (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-20170182015-A1 METHODS OF USING SNS-595 FOR TREATMENT OF CANCER SUBJECTS WITH REDUCED BRCA2 ACTIVITY BRCA1, MRE11, RAD51 HTR3A 668/4885LMNA 964/4885KMT2A 2551/4885
US-20100203162-A1 Method of preparing (+)-1,4-dihydro-7-[(3S,4S)-3-methoxy-4-(methylamino)-1-pyrrolidinyl]-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3-carboxylic acid CYP7A1, MT-ND1, DNM1 HTR3A 513/4885LMNA 961/4885KMT2A 2993/4885
US-20120148564-A1 METHODS OF USING SNS-595 FOR TREATMENT OF CANCER SUBJECTS WITH REDUCED BRCA2 ACTIVITY BRCA1, MRE11, RAD51 HTR3A 668/4885LMNA 964/4885KMT2A 2551/4885
US-20100029708-A1 COMPOUNDS AND COMPOSITIONS FOR TREATMENT OF CANCER NTPCR, NNMT, NES HTR3A 2134/4885LMNA 546/4885KMT2A 3277/4885

“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.