SCHEMBL2478683

SCHEMBL2478683

Nc1ccc(Cl)c(Cl)c1CNCC(=O)O

nearest known ligand 0.37

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
CA1 P00915 7/20 0.35
CA2 P00918 7/20 0.35
FFAR4 Q5NUL3 1/20 0.35
HDAC1 Q13547 2/20 0.34
KDM4E B2RXH2 1/20 0.33
MAPT P10636 1/20 0.33
HIF1A Q16665 1/20 0.33
SLC22A6 Q4U2R8 1/20 0.33
SLC22A8 Q8TCC7 1/20 0.33
AKR1B1 P15121 1/20 0.33
FFAR1 O14842 1/20 0.33
GRIN1 Q05586 1/20 0.32

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
SCHEMBL11552559 0.83 SMN1; SMN2 (0.37) CA1CA2KDM4EMAPT
Hydrochloric Acid SCHEMBL5710314 0.82 SMN1; SMN2 (0.36) KDM4EMAPT
SCHEMBL28207903 0.81 CA1 (0.36) CA1CA2HDAC1HIF1AGRIN1
SCHEMBL278947 0.80 PPID (0.42) KDM4EMAPT
SCHEMBL30505642 0.80 PPID (0.42) KDM4EMAPT
SCHEMBL11550553 0.79 TSHR (0.37) KDM4EMAPT
Hydrochloric Acid SCHEMBL27767646 0.79 PPID (0.41) KDM4EMAPT
SCHEMBL28212935 0.79 VSIR (0.37) CA1MAPT
Hydrochloric Acid SCHEMBL5710126 0.79 PPID (0.41) KDM4EMAPT
SCHEMBL10603639 0.78 KDM4E (0.42) KDM4EMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0514917-B1 Process for and 2-(cyanoimino)-quinazoline derivatives useful as intermediates in the preparation of 6,7-di-(chloro)-1,5-di(hydro)-imidazo-[2,1-b]quinazolin-2[3H]-one and process for preparing the 2-(cyanoimino)-quinazoline derivatives EGYT GYOGYSZERVEGYESZETI GYAR (HU) 1996-12-27 EP claimed
EP-0514917-A1 Process for and 2-(cyanoimino)-quinazoline derivatives useful as intermediates in the preparation of 6,7-di-(chloro)-1,5-di(hydro)-imidazo-[2,1-b]quinazolin-2[3H]-one and process for preparing the 2-(cyanoimino)-quinazoline derivatives EGIS GYOGYSZERGYAR (HU) 1992-11-25 EP claimed
JP-5271200-A None JP disclosed
EP-2630148-B1 PROCESS FOR THE PREPARATION OF ANAGRELIDE AND ANALOGUES THEREOF SHIRE LLC (US) 2020-11-25 EP disclosed
CN-107903217-A A kind of preparation method of anagrelide impurity B 湖北省宏源药业科技股份有限公司 2018-04-13 CN disclosed
CN-103180323-B For the method preparing anagrelide and the like 夏尔有限责任公司 2016-08-10 CN disclosed
US-8530651-B2 Process for the preparation of anagrelide and analogues SHIRE LLC (US) 2013-09-10 US disclosed
EP-2630148-A1 PROCESS FOR THE PREPARATION OF ANAGRELIDE AND ANALOGUES THEREOF Shire LLC (US) 2013-08-28 EP disclosed
CN-103180323-A Process for the preparation of anagrelide and analogues thereof SHIRE LLC 2013-06-26 CN disclosed
WO-2012052781-A1 PROCESS FOR THE PREPARATION OF ANAGRELIDE AND ANALOGUES THEREOF SHIRE, LLC (US) 2012-04-26 WO disclosed
CN-102256981-A Process for the preparation of anagrelide and analogues SHIRE LLC 2011-11-23 CN disclosed
US-6653500-B2 Making ethyl N-(2,3-dichloro-6-nitrobenzyl)glycine from 2,3-dichlorobenzaldehyde, reducing the glycine compound using tin dichloride or a catalyst and cyclization of the corresponding iminoquinazoline compound SHIRE US INC. 2003-11-25 US disclosed
US-20030060630-A1 Method for the manufacture of Anagrelide SHIRE US INC. 2003-03-27 US disclosed
US-6388073-B1 NITRATION A 3,4-DICHLOROBENZALDEHYDE; REDUCING; CHLORINATION; ALKYLATION; BROMOCYANATION; CHLIZATION SHIRE US INC. 2002-05-14 US disclosed
WO-2002008228-A2 METHOD FOR THE MANUFACTURE OF ANAGRELIDE SHIRE US INC (US) 2002-01-31 WO disclosed
EP-0514917-B1 Process for and 2-(cyanoimino)-quinazoline derivatives useful as intermediates in the preparation of 6,7-di-(chloro)-1,5-di(hydro)-imidazo-[2,1-b]quinazolin-2[3H]-one and process for preparing the 2-(cyanoimino)-quinazoline derivatives EGYT GYOGYSZERVEGYESZETI GYAR (HU) 1996-12-27 EP disclosed
US-5391737-A Process for the preparation of 6,7-dichloro-1,5-dihydroimidazo[2,1-b]quinazolin-2[3H]-one EGIS GYOGYSZERGYAR (HU) 1995-02-21 US disclosed
JP-H05271200-A PRODUCTION OF 6,7-DICHLORO-1,5-DIHYDRO-IMIDAZO(2,1-B)QUINAZOLIN-2(3H)-ONE EGYT GYOGYSZERVEGYESZETI GYAR 1993-10-19 JP disclosed
EP-0514917-A1 Process for and 2-(cyanoimino)-quinazoline derivatives useful as intermediates in the preparation of 6,7-di-(chloro)-1,5-di(hydro)-imidazo-[2,1-b]quinazolin-2[3H]-one and process for preparing the 2-(cyanoimino)-quinazoline derivatives EGIS GYOGYSZERGYAR (HU) 1992-11-25 EP disclosed
US-4146718-A BLOOD PLATELET ANTIAGGREGATIVE AGENT BRISTOL-MYERS COMPANY (US) 1979-03-27 US 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 (1 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-20030060630-A1 Method for the manufacture of Anagrelide SUCLG2, PDCD2L, ICOSLG CA1 4119/4885CA2 3760/4885FFAR4 4711/4885

“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.