SCHEMBL3018059

SCHEMBL3018059

O=S(=O)(c1ccc(Br)cc1)n1cccc1

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA2 P00918 4/20 0.64
CA1 P00915 2/20 0.64
GAA P10253 1/20 0.51
MEN1 O00255 1/20 0.51
PKM P14618 1/20 0.51
HTT P42858 1/20 0.51
KMT2A Q03164 1/20 0.51
L3MBTL1 Q9Y468 1/20 0.51
FBP1 P09467 1/20 0.51
MMP2 P08253 4/20 0.50
PLCG1 P19174 1/20 0.45
LMNA P02545 1/20 0.42
CTSG P08311 1/20 0.42
CMA1 P23946 1/20 0.42
IDO1 P14902 1/20 0.42
CA12 O43570 1/20 0.42
CA9 Q16790 1/20 0.42
MMP1 P03956 1/20 0.42
MMP9 P14780 1/20 0.42
MMP8 P22894 1/20 0.42

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
SCHEMBL752816 0.79 CA1 (0.65) CA2CA1MEN1PKMHTT
SCHEMBL1364805 0.78 CA1 (1.00) CA2CA1GAAPKMHTT
SCHEMBL6765743 0.78 CA1 (0.58) CA2CA1GAAMEN1PKM
SCHEMBL5592750 0.75 GAA (0.57) CA2CA1GAAMEN1PKM
SCHEMBL16059915 0.74 CA1 (0.59) CA2CA1MEN1PKMHTT
SCHEMBL12419386 0.74 CA2 (0.58) CA2CA1PKMFBP1
SCHEMBL15315388 0.74 CA2 (0.58) CA2CA1FBP1MMP2LMNA
SCHEMBL2181734 0.74 CA1 (0.58) CA2CA1GAAMEN1KMT2A
SCHEMBL9344505 0.71 ALDH1A1 (0.65) PKMHTTMMP2LMNA
SCHEMBL31315858 0.71 ALDH1A1 (0.65) PKMHTTMMP2LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107245023-B A kind of selectivity deoxofluorination reagent and method 中国科学院上海有机化学研究所 2019-08-16 CN disclosed
CN-107245023-A A kind of selective deoxofluorination reagent and method 中国科学院上海有机化学研究所 2017-10-13 CN disclosed
EP-2812332-B1 METHODS FOR THE PREPARATION OF HIV ATTACHMENT INHIBITOR PIPERAZINE PRODRUG COMPOUND VIIV HEALTHCARE UK (NO 4) LTD (GB) 2017-08-09 EP disclosed
US-9403821-B2 Methods for the preparation of HIV attachment inhibitor piperazine prodrug compound BRISTOL-MYERS SQUIBB COMPANY (US) 2016-08-02 US disclosed
US-9403821-B2 Methods for the preparation of HIV attachment inhibitor piperazine prodrug compound BRISTOL-MYERS SQUIBB COMPANY (US) 2016-08-02 US disclosed
US-9394322-B2 Methods for the preparation of HIV attachment inhibitor piperazine prodrug compound BRISTOL-MYERS SQUIBB COMPANY (US) 2016-07-19 US disclosed
US-9394322-B2 Methods for the preparation of HIV attachment inhibitor piperazine prodrug compound BRISTOL-MYERS SQUIBB COMPANY (US) 2016-07-19 US disclosed
US-9376458-B2 Methods for the preparation of HIV attachment inhibitor piperazine prodrug compound BRISTOL-MYERS SQUIBB COMPANY (US) 2016-06-28 US disclosed
US-9376458-B2 Methods for the preparation of HIV attachment inhibitor piperazine prodrug compound BRISTOL-MYERS SQUIBB COMPANY (US) 2016-06-28 US disclosed
US-20160152644-A1 METHODS FOR THE PREPARATION OF HIV ATTACHMENT INHIBITOR PIPERAZINE PRODRUG COMPOUND VIIV HEALTHCARE UK (NO. 4) LIMITED (GB) 2016-06-02 US disclosed
WO-2013119625-A1 METHODS FOR THE PREPARATION OF HIV ATTACHMENT INHIBITOR PIPERAZINE PRODRUG COMPOUND BRISTOL-MYERS SQUIBB COMPANY (US) 2013-08-15 WO disclosed
US-20130203992-A1 METHODS FOR THE PREPARATION OF HIV ATTACHMENT INHIBITOR PIPERAZINE PRODRUG COMPOUND BRISTOL-MYERS SQUIBB COMPANY (US) 2013-08-08 US disclosed
US-20130203992-A1 METHODS FOR THE PREPARATION OF HIV ATTACHMENT INHIBITOR PIPERAZINE PRODRUG COMPOUND BRISTOL-MYERS SQUIBB COMPANY (US) 2013-08-08 US disclosed
US-20100204228-A1 Aryl Sulfonamides Useful for Modulation of the Progesterone Receptor WYETH LLC (US) 2010-08-12 US disclosed
US-7723332-B2 Aryl sulfonamides useful for modulation of the progesterone receptor WYETH LLC (US) 2010-05-25 US disclosed
EP-2137145-A2 CYANOPYRROL SULFONAMIDES USEFUL FOR MODULATION OF THE PROGESTERONE RECEPTOR Wyeth (US) 2009-12-30 EP disclosed
WO-2008109055-A2 CYANOPYRROLE SULFONAMIDES USEFUL FOR MODULATION OF THE PROGESTERONE RECEPTOR WYETH (US) 2008-09-12 WO disclosed
US-20080221201-A1 4-(5-cyano-1-methyl-1H-pyrrol-2-yl)-N-methylbenzenesulfonamide; contraception, treating or preventing fibroids, uterine leiomyomata, endometriosis, dysfunctional bleeding, polycystic ovary syndrome, or hormone-dependent carcinomas, providing hormone replacement therapy, stimulating food intake WYETH (US) 2008-09-11 US disclosed
CN-100363348-C PgD2 receptor antagonists for the treatment of inflammatory diseases MILLENNIUM PHARM INC (US) 2008-01-23 CN disclosed
CN-1720047-A PgD2 receptor antagonists for the treatment of inflammatory diseases MILLENNIUM PHARM INC (US) 2006-01-11 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 (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-20160152644-A1 METHODS FOR THE PREPARATION OF HIV ATTACHMENT INHIBITOR PIPERAZINE PRODRUG COMPOUND FURIN, NAPA, PREP CA2 4276/4885CA1 3943/4885GAA 1596/4885
US-20130203992-A1 METHODS FOR THE PREPARATION OF HIV ATTACHMENT INHIBITOR PIPERAZINE PRODRUG COMPOUND FURIN, NAPA, PREP CA2 4276/4885CA1 3943/4885GAA 1596/4885
US-20100204228-A1 Aryl Sulfonamides Useful for Modulation of the Progesterone Receptor FSHR, GNRHR, CYP19A1 CA2 2013/4885CA1 1620/4885GAA 4842/4885
US-20080221201-A1 4-(5-cyano-1-methyl-1H-pyrrol-2-yl)-N-methylbenzenesulfonamide; contraception, treating or preventing fibroids, uterine leiomyomata, endometriosis, dysfunctional bleeding, polycystic ovary syndrome, or hormone-dependent carcinomas, providing hormone replacement therapy, stimulating food intake PKD1, PKD2, SHBG CA2 2127/4885CA1 1757/4885GAA 4879/4885

“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.