SCHEMBL5713

SCHEMBL5713

C=Cc1ccc(Br)cc1OC

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 2/20 0.43
KMT2A Q03164 2/20 0.43
CYP1A1 P04798 3/20 0.42
CYP1A2 P05177 3/20 0.42
CYP1B1 Q16678 3/20 0.42
ERN1 O75460 1/20 0.41
TUBB4A P04350 1/20 0.41
TUBB P07437 1/20 0.41
TUBA3C P0DPH7 1/20 0.41
TUBA1B P68363 1/20 0.41
TUBA4A P68366 1/20 0.41
TUBB4B P68371 1/20 0.41
TUBB3 Q13509 1/20 0.41
TUBB2A Q13885 1/20 0.41
TUBB8 Q3ZCM7 1/20 0.41
TUBA3E Q6PEY2 1/20 0.41
TUBA1A Q71U36 1/20 0.41
TUBA1C Q9BQE3 1/20 0.41
TUBB6 Q9BUF5 1/20 0.41
TUBB2B Q9BVA1 1/20 0.41

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
SCHEMBL129594 0.84 AMY1A (0.51) MEN1KMT2ACYP1A2AMY1AALDH1A1
SCHEMBL21352066 0.82 TUBB4A (0.46) MEN1KMT2ACYP1A1CYP1A2CYP1B1
SCHEMBL2044950 0.80 KDM4E (0.40) MEN1KMT2ACYP1A1CYP1A2CYP1B1
SCHEMBL7672288 0.80 CYP1A1 (0.42) MEN1KMT2ACYP1A1CYP1A2CYP1B1
SCHEMBL30178662 0.80 ALDH1A1 (0.63) CYP1A1CYP1A2CYP1B1ERN1ALDH1A1
SCHEMBL11173 0.80 ALDH1A1 (0.63) CYP1A1CYP1A2CYP1B1ERN1ALDH1A1
SCHEMBL3810446 0.79 ALDH1A1 (0.43) MEN1KMT2AALDH1A1LMNASMN1; SMN2
SCHEMBL3861430 0.79 HPGD (0.51) MEN1KMT2AALDH1A1LMNASMN1; SMN2
SCHEMBL24851672 0.79 ALDH1A1 (0.48) CYP1A1CYP1A2CYP1B1ERN1ALDH1A1
SCHEMBL10515789 0.78 CYP1A2 (0.50) MEN1KMT2ACYP1A1CYP1A2CYP1B1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2836490-B1 INDOLE AND INDAZOLE COMPOUNDS THAT ACTIVATE AMPK PFIZER (US) 2017-06-14 EP disclosed
US-9394285-B2 Indole and indazole compounds that activate AMPK PFIZER INC. (US) 2016-07-19 US disclosed
US-20160016940-A1 Indole and Indazole Compounds that Activate AMPK PFIZER, INC. (US) 2016-01-21 US disclosed
EP-2970177-A1 INDOLE COMPOUNDS THAT ACTIVATE AMPK Pfizer Inc. (US) 2016-01-20 EP disclosed
EP-2836490-A2 INDOLE AND INDAZOLE COMPOUNDS THAT ACTIVATE AMPK Pfizer Inc. (US) 2015-02-18 EP disclosed
US-20150038484-A1 INDOLE AND INDAZOLE COMPOUNDS THAT ACTIVATE AMPK PFIZER INC. (US) 2015-02-05 US disclosed
US-20140364398-A1 C-Linked Hydroxamic Acid Derivatives Useful As Antibacterial Agents PFIZER INC. (US) 2014-12-11 US disclosed
US-20140364398-A1 C-Linked Hydroxamic Acid Derivatives Useful As Antibacterial Agents PFIZER INC. (US) 2014-12-11 US disclosed
US-20140364398-A1 C-Linked Hydroxamic Acid Derivatives Useful As Antibacterial Agents PFIZER INC. (US) 2014-12-11 US disclosed
US-8889730-B2 Indole and indazole compounds that activate AMPK PFIZER INC. (US) 2014-11-18 US disclosed
US-8853258-B2 C-linked hydroxamic acid derivatives useful as antibacterial agents PFIZER INC. (US) 2014-10-07 US disclosed
WO-2014140704-A1 INDOLE COMPOUNDS THAT ACTIVATE AMPK PFIZER INC. (US) 2014-09-18 WO disclosed
WO-2013153479-A2 INDOLE AND INDAZOLE COMPOUNDS THAT ACTIVATE AMPK PFIZER INC. (US) 2013-10-17 WO disclosed
US-20130267493-A1 INDOLE AND INDAZOLE COMPOUNDS THAT ACTIVATE AMPK PFIZER INC. (US) 2013-10-10 US disclosed
EP-2488489-A2 C-LINKED HYDROXAMIC ACID DERIVATIVES USEFUL AS ANTIBACTERIAL AGENTS Pfizer Inc. (US) 2012-08-22 EP disclosed
US-20120202777-A1 C-Linked Hydroxamic Acid Derivatives Useful As Antibacterial Agents BROWN MATTHEW FRANK (US) 2012-08-09 US disclosed
US-20120202777-A1 C-Linked Hydroxamic Acid Derivatives Useful As Antibacterial Agents BROWN MATTHEW FRANK (US) 2012-08-09 US disclosed
US-20120202777-A1 C-Linked Hydroxamic Acid Derivatives Useful As Antibacterial Agents BROWN MATTHEW FRANK (US) 2012-08-09 US disclosed
WO-2011045703-A2 C-LINKED HYDROXAMIC ACID DERIVATIVES USEFUL AS ANTIBACTERIAL AGENTS PFIZER INC. (US) 2011-04-21 WO disclosed
WO-2011045703-A2 C-LINKED HYDROXAMIC ACID DERIVATIVES USEFUL AS ANTIBACTERIAL AGENTS PFIZER INC. (US) 2011-04-21 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 (5 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-20120202777-A1 C-Linked Hydroxamic Acid Derivatives Useful As Antibacterial Agents HAX1, LPXN, AGXT MEN1 4345/4885KMT2A 387/4885CYP1A1 3767/4885
US-20160016940-A1 Indole and Indazole Compounds that Activate AMPK PRKAG1, PRKAG3, PRKAG2 MEN1 4037/4885KMT2A 1740/4885CYP1A1 858/4885
US-20150038484-A1 INDOLE AND INDAZOLE COMPOUNDS THAT ACTIVATE AMPK PRKAG1, PRKAG3, PRKAG2 MEN1 4037/4885KMT2A 1740/4885CYP1A1 858/4885
US-20130267493-A1 INDOLE AND INDAZOLE COMPOUNDS THAT ACTIVATE AMPK PRKAG1, PRKAG3, PRKAG2 MEN1 4037/4885KMT2A 1740/4885CYP1A1 858/4885
US-20140364398-A1 C-Linked Hydroxamic Acid Derivatives Useful As Antibacterial Agents LCT, AGXT, PRXL2A MEN1 4357/4885KMT2A 636/4885CYP1A1 4461/4885

“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.