SCHEMBL2564080

SCHEMBL2564080

OB(O)c1ccccc1-c1nnn(C(c2ccccc2)(c2ccccc2)c2ccccc2)n1

nearest known ligand 0.46

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.37
POLB P06746 1/20 0.37
AGTR1 P30556 1/20 0.35
ABCG2 Q9UNQ0 4/20 0.34
PDK2 Q15119 1/20 0.32
NPC1 O15118 3/20 0.32
RAB9A P51151 3/20 0.32
MAPT P10636 2/20 0.31
PKM P14618 1/20 0.31
HPGD P15428 2/20 0.31
L3MBTL1 Q9Y468 1/20 0.31
ABCB1 P08183 1/20 0.31
ALDH1A1 P00352 1/20 0.30

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
SCHEMBL29954781 1.00 SMN1; SMN2 (0.37) SMN1; SMN2POLBAGTR1ABCG2PDK2
SCHEMBL4888374 0.87 POLB (0.39) SMN1; SMN2POLBABCG2PDK2NPC1
SCHEMBL9257119 0.84 POLB (0.40) SMN1; SMN2POLBABCG2PDK2NPC1
SCHEMBL14169541 0.83 POLB (0.34) SMN1; SMN2POLBAGTR1
SCHEMBL30743612 0.79 ABCG2 (0.55) SMN1; SMN2POLBAGTR1ABCG2NPC1
SCHEMBL16370823 0.78 AGTR1 (0.43) SMN1; SMN2POLBAGTR1ABCG2NPC1
SCHEMBL9429714 0.78 ABCG2 (0.36) SMN1; SMN2POLBAGTR1ABCG2NPC1
SCHEMBL4990435 0.78 SMN1; SMN2 (0.36) SMN1; SMN2POLBABCG2NPC1RAB9A
SCHEMBL8402419 0.77 POLB (0.40) SMN1; SMN2POLBAGTR1ABCG2NPC1
SCHEMBL9033772 0.77 AGTR1 (0.41) SMN1; SMN2POLBAGTR1ABCG2NPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11225655-B2 Bi-functional complexes and methods for making and using such complexes NUEVOLUTION A/S (DK) 2022-01-18 US disclosed
EP-3540059-A1 BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES Nuevolution A/S (DK) 2019-09-18 EP disclosed
EP-2558577-B1 BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES NUEVOLUTION AS (DK) 2018-12-12 EP disclosed
US-20130281324-A1 BI-FUNCTINAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES NUEVOLUTION A/S (DK) 2013-10-24 US disclosed
EP-2558577-A1 BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES Nuevolution A/S (DK) 2013-02-20 EP disclosed
WO-2011127933-A1 BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES NUEVOLUTION A/S (DK) 2011-10-20 WO disclosed
US-7915425-B2 Process for the preparation of losartan SUVEN LIFE SCIENCES LIMITED (IN) 2011-03-29 US disclosed
US-7915425-B2 Process for the preparation of losartan SUVEN LIFE SCIENCES LIMITED (IN) 2011-03-29 US disclosed
US-20100222597-A1 Process for the preparation of losartan SUVEN LIFE SCIENCES LIMITED (IN) 2010-09-02 US disclosed
US-20100222597-A1 Process for the preparation of losartan SUVEN LIFE SCIENCES LIMITED (IN) 2010-09-02 US disclosed
US-20080132555-A1 PREPARATION AND UTILITY OF SUBSTITUTED PHENYLTETRAZOLES AUSPEX PHARMACEUTICALS, INC. (US) 2008-06-05 US disclosed
US-20080132555-A1 PREPARATION AND UTILITY OF SUBSTITUTED PHENYLTETRAZOLES AUSPEX PHARMACEUTICALS, INC. (US) 2008-06-05 US disclosed
US-20080132555-A1 PREPARATION AND UTILITY OF SUBSTITUTED PHENYLTETRAZOLES AUSPEX PHARMACEUTICALS, INC. (US) 2008-06-05 US disclosed
WO-2008067378-A2 PREPARATION AND UTILITY OF SUBSTITUTED PHENYLTETRAZOLES AUSPEX PHARMACEUTICALS, INC. (US) 2008-06-05 WO disclosed
US-20070249839-A1 Process for the Preparation of Losartan Potassium Form I CADILA PHARMACEUTICALS LTD. (IN) 2007-10-25 US disclosed
US-20070249839-A1 Process for the Preparation of Losartan Potassium Form I CADILA PHARMACEUTICALS LTD. (IN) 2007-10-25 US disclosed
US-6245790-B1 ANTIINFLAMMATORY AGENTS; GASTROINTESTINAL DISORDERS; SKN DISORDERS; BONE DISORDERS; MUSCLE RELAXANTS FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2001-06-12 US disclosed
EP-0989975-A1 OXAZOLE COMPOUNDS USEFUL AS PGE2 AGONISTS AND ANTAGONISTS FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2000-04-05 EP disclosed
WO-2000016760-A2 NEW USE OF PROSTAGLANDIN E2 ANTAGONISTS FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2000-03-30 WO disclosed
WO-1998055468-A1 OXAZOLE COMPOUNDS USEFUL AS PGE2 AGONISTS AND ANTAGONISTS FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1998-12-10 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-20080132555-A1 PREPARATION AND UTILITY OF SUBSTITUTED PHENYLTETRAZOLES CYP3A7, CYP3A5, CYP2C19 SMN1; SMN2 2795/4885POLB 1897/4885AGTR1 2103/4885
US-20070249839-A1 Process for the Preparation of Losartan Potassium Form I AGTR1, REN, AGT SMN1; SMN2 4434/4885POLB 3372/4885AGTR1 1/4885
US-20100222597-A1 Process for the preparation of losartan AGT, ACE, AGTR1 SMN1; SMN2 3914/4885POLB 1585/4885AGTR1 3/4885

“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.