Methacycline

Methacycline

SCHEMBL5523818

C=C1c2cccc(O)c2C(=O)C2=C(O)[C@]3(O)C(=O)C(C(N)=O)=C(O)[C@@H](N(C)C)C3[C@@H](O)C12

nearest known ligand 0.70

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

rplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Methacycline. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 13/20 0.70
KDM4E B2RXH2 10/20 0.70
USP2 O75604 9/20 0.70
RECQL P46063 8/20 0.70
HPGD P15428 8/20 0.70
HSD17B10 Q99714 8/20 0.70
THRB P10828 6/20 0.70
LMNA P02545 3/20 0.70
NR1I2 O75469 2/20 0.70
SIRT5 Q9NXA8 2/20 0.70
MC4R P32245 1/20 0.70
MEN1 O00255 7/20 0.69
KMT2A Q03164 7/20 0.69
MAPT P10636 6/20 0.69
L3MBTL1 Q9Y468 6/20 0.69
POLB P06746 3/20 0.69
RAD52 P43351 1/20 0.69
ALDH1A1 P00352 6/20 0.49
HIF1A Q16665 3/20 0.49
TSHR P16473 1/20 0.49

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
Methacycline SCHEMBL21133469 1.00 TDP1 (0.70) TDP1KDM4EUSP2RECQLHPGD
Methacycline SCHEMBL4014 1.00 TDP1 (0.70) TDP1KDM4EUSP2RECQLHPGD
Methacycline SCHEMBL13328119 1.00 TDP1 (0.70) TDP1KDM4EUSP2RECQLHPGD
Methacycline SCHEMBL4016 1.00 TDP1 (0.70) TDP1KDM4EUSP2RECQLHPGD
Methacycline SCHEMBL19771282 1.00 TDP1 (0.70) TDP1KDM4EUSP2RECQLHPGD
Methacycline SCHEMBL17430778 1.00 TDP1 (0.70) TDP1KDM4EUSP2RECQLHPGD
Methacycline SCHEMBL2614978 1.00 TDP1 (0.70) TDP1KDM4EUSP2RECQLHPGD
Methacycline SCHEMBL29376851 1.00 TDP1 (0.70) TDP1KDM4EUSP2RECQLHPGD
Methacycline SCHEMBL127703 0.99 TDP1 (0.70) TDP1KDM4EUSP2RECQLHPGD
Methacycline SCHEMBL5445227 0.99 TDP1 (0.70) TDP1KDM4EUSP2RECQLHPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20190040001-A1 METHODS OF USING SUBSTITUTED TETRACYCLINE COMPOUNDS TO MODULATE RNA PARATEK PHARMACEUTICALS, INC. 2019-02-07 US disclosed
US-20180016225-A1 TETRACYCLINE COMPOUNDS HAVING TARGET THERAPEUTIC ACTIVITIES PARATEK PHARMACEUTICALS, INC. 2018-01-18 US disclosed
US-20180016225-A1 TETRACYCLINE COMPOUNDS HAVING TARGET THERAPEUTIC ACTIVITIES PARATEK PHARMACEUTICALS, INC. 2018-01-18 US disclosed
US-9562003-B2 Methods of using substituted tetracycline compounds to modulate RNA PARATEK PHARMACEUTICALS, INC. (US) 2017-02-07 US disclosed
US-9562003-B2 Methods of using substituted tetracycline compounds to modulate RNA PARATEK PHARMACEUTICALS, INC. (US) 2017-02-07 US disclosed
US-20150321997-A1 METHODS OF USING SUBSTITUTED TETRACYCLINE COMPOUNDS TO MODULATE RNA PARATEK PHARMACEUTICALS, INC. (US) 2015-11-12 US disclosed
US-20150321997-A1 METHODS OF USING SUBSTITUTED TETRACYCLINE COMPOUNDS TO MODULATE RNA PARATEK PHARMACEUTICALS, INC. (US) 2015-11-12 US disclosed
US-20150141381-A1 TETRACYCLINE COMPOUNDS HAVING TARGET THERAPEUTIC ACTIVITIES PARATEK PHARMACEUTICALS, INC. (US) 2015-05-21 US disclosed
US-20150141381-A1 TETRACYCLINE COMPOUNDS HAVING TARGET THERAPEUTIC ACTIVITIES PARATEK PHARMACEUTICALS, INC. (US) 2015-05-21 US disclosed
US-20140343020-A1 METHODS OF USING SUBSTITUTED TETRACYCLINE COMPOUNDS TO MODULATE RNA PARATEK PHARMACEUTICALS, INC (US) 2014-11-20 US disclosed
US-7960366-B2 Tetracycline compound of given formula, an antifungal agent such as amphotericin B and a carrier; treating fungal infections PARATEK PHARMACEUTICALS, INC. (US) 2011-06-14 US disclosed
US-7960366-B2 Tetracycline compound of given formula, an antifungal agent such as amphotericin B and a carrier; treating fungal infections PARATEK PHARMACEUTICALS, INC. (US) 2011-06-14 US disclosed
US-7696187-B2 Methods of preparing substituted tetracyclines with transition metal-based chemistries TRUSTEES OF TUFTS COLLEGE (US) 2010-04-13 US disclosed
US-7696187-B2 Methods of preparing substituted tetracyclines with transition metal-based chemistries TRUSTEES OF TUFTS COLLEGE (US) 2010-04-13 US disclosed
US-7414041-B2 Reducing tetracycline resistance in living cells TRUSTEES OF TUFTS COLLEGE (US) 2008-08-19 US disclosed
US-20080118979-A1 Methods of regulating expression of genes or of gene products using substituted tetracycline compounds PARATEK PHARMACEUTICALS, INC. (US) 2008-05-22 US disclosed
US-20080118979-A1 Methods of regulating expression of genes or of gene products using substituted tetracycline compounds PARATEK PHARMACEUTICALS, INC. (US) 2008-05-22 US disclosed
US-20070072834-A1 13-Substituted methacycline compounds PARATEK PHARMACEUTICALS, INC. (US) 2007-03-29 US disclosed
US-20070072834-A1 13-Substituted methacycline compounds PARATEK PHARMACEUTICALS, INC. (US) 2007-03-29 US disclosed
WO-2004038000-A2 METHODS OF USING SUBSTITUTED TETRACYCLINE COMPOUNDS TO MODULATE RNA PARATEK PHARMACEUTICALS, INC. (US) 2004-05-06 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 (6 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-20150321997-A1 METHODS OF USING SUBSTITUTED TETRACYCLINE COMPOUNDS TO MODULATE RNA NSUN3, NSUN2, RNMT TDP1 999/4885KDM4E 1013/4885USP2 1487/4885
US-20190040001-A1 METHODS OF USING SUBSTITUTED TETRACYCLINE COMPOUNDS TO MODULATE RNA NSUN3, NSUN2, RNMT TDP1 999/4885KDM4E 1013/4885USP2 1487/4885
US-20140343020-A1 METHODS OF USING SUBSTITUTED TETRACYCLINE COMPOUNDS TO MODULATE RNA NSUN3, NSUN2, RNMT TDP1 999/4885KDM4E 1013/4885USP2 1487/4885
US-20070072834-A1 13-Substituted methacycline compounds TET3, TET1, TPMT TDP1 2190/4885KDM4E 1560/4885USP2 2846/4885
US-20180016225-A1 TETRACYCLINE COMPOUNDS HAVING TARGET THERAPEUTIC ACTIVITIES TBCA, TUBB6, TUBB TDP1 1003/4885KDM4E 3572/4885USP2 2358/4885
US-20150141381-A1 TETRACYCLINE COMPOUNDS HAVING TARGET THERAPEUTIC ACTIVITIES TBCA, TUBB6, TUBB TDP1 1003/4885KDM4E 3572/4885USP2 2358/4885

“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.