Minocycline

Minocycline

SCHEMBL1917128

CN(C)c1ccc(O)c2c1CC1CC3[C@H](N(C)C)C(O)=C(C(N)=O)C(=O)[C@@]3(O)C(O)=C1C2=O

nearest known ligand 0.70

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

rplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Minocycline. 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 9/20 0.70
▸ KDM4E B2RXH2 6/20 0.70
▸ USP2 O75604 4/20 0.70
▸ HIF1A Q16665 3/20 0.70
▸ PTGS1 P23219 2/20 0.70
▸ GRK6 P43250 1/20 0.70
▸ ABCB11 O95342 1/20 0.70
▸ ALB P02768 1/20 0.70
▸ MAPT P10636 6/20 0.69
▸ HPGD P15428 2/20 0.69
▸ CYP3A4 P08684 2/20 0.69
▸ RECQL P46063 2/20 0.69
▸ HSD17B10 Q99714 4/20 0.61
▸ THPO P40225 1/20 0.61
▸ KMT2A Q03164 7/20 0.60
▸ LMNA P02545 3/20 0.60
▸ BLM P54132 1/20 0.60
▸ NR1I2 O75469 3/20 0.48
▸ ADORA3 P0DMS8 2/20 0.48
▸ CHRM1 P11229 2/20 0.48

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
Minocycline SCHEMBL9340562 1.00 TDP1 (0.70) TDP1KDM4EUSP2HIF1APTGS1
Minocycline SCHEMBL13520108 1.00 TDP1 (0.70) TDP1KDM4EUSP2HIF1APTGS1
Minocycline SCHEMBL1820770 1.00 TDP1 (0.70) TDP1KDM4EUSP2HIF1APTGS1
Minocycline SCHEMBL13520109 1.00 TDP1 (0.70) TDP1KDM4EUSP2HIF1APTGS1
Minocycline SCHEMBL12532767 1.00 TDP1 (0.70) TDP1KDM4EUSP2HIF1APTGS1
Minocycline SCHEMBL13520116 1.00 TDP1 (0.70) TDP1KDM4EUSP2HIF1APTGS1
Minocycline SCHEMBL22171064 1.00 TDP1 (0.70) TDP1KDM4EUSP2HIF1APTGS1
Minocycline SCHEMBL20716523 1.00 TDP1 (0.70) TDP1KDM4EUSP2HIF1APTGS1
Minocycline SCHEMBL21931671 1.00 TDP1 (0.70) TDP1KDM4EUSP2HIF1APTGS1
Minocycline SCHEMBL11911315 1.00 TDP1 (0.70) TDP1KDM4EUSP2HIF1APTGS1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240238315-A1 MINOCYCLINE COMPOUNDS FOR BIODEFENSE PARATEK PHARM INNC (US) 2024-07-18 — — US disclosed
US-20240238315-A1 MINOCYCLINE COMPOUNDS FOR BIODEFENSE PARATEK PHARM INNC (US) 2024-07-18 — — US disclosed
US-20210395189-A1 SUBSTITUTED TETRACYCLINE COMPOUNDS PARATEK PHARMACEUTICALS, INC. 2021-12-23 — — US disclosed
US-11129839-B2 Minocycline compounds for biodefense PARATEK PHARMACEUTICALS, INC. (US) 2021-09-28 — — US disclosed
US-20200330489-A1 MINOCYCLINE COMPOUNDS FOR BIODEFENSE PARATEK PHARMACEUTICALS, INC. 2020-10-22 — — US disclosed
WO-2020135508-A1 MINOCYCLINE(II) P-CHLOROBENZENE SULFONATE CRYSTAL FORM, PREPARATION METHOD THEREFOR AND USE THEREOF 浙江昌海制药有限公司 2020-07-02 — — WO disclosed
US-10252984-B2 Inhibiting G protein coupled receptor 6 kinase polypeptides MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH (US) 2019-04-09 — — US disclosed
US-20180133231-A1 MINOCYCLINE COMPOUNDS FOR BIODEFENSE PARATEK PHARMACEUTICALS, INC. 2018-05-17 — — US disclosed
US-20180133231-A1 MINOCYCLINE COMPOUNDS FOR BIODEFENSE PARATEK PHARMACEUTICALS, INC. 2018-05-17 — — US disclosed
US-20180104262-A1 SALTS AND POLYMORPHS OF A TETRACYCLINE COMPOUND PARATEK PHARMACEUTICALS, INC. 2018-04-19 — — US disclosed
US-20080287401-A1 Methods for Synthesizing and Purifying Aminoalkyl Tetracycline Compounds PARATEK PHARMACEUTICALS, INC. 2008-11-20 — — US disclosed
WO-2008079339-A2 TETRACYCLINE DERIVATIVES FOR THE TREATMENT OF BACTERIAL, VIRAL AND PARASITIC INFECTIONS PARATEK PHARMACEUTICALS, INC. (US) 2008-07-03 — — WO disclosed
EP-1890997-A1 METHODS OF PURIFYING TIGECYCLINE Wyeth a Corporation of the State of Delaware (US) 2008-02-27 — — EP disclosed
WO-2008020827-A2 ALTERED POLYPEPTIDES, IMMUNOCONJUGATES THEREOF, AND METHODS RELATED THERETO BIOGEN IDEC MA INC. (US) 2008-02-21 — — WO disclosed
US-20070248988-A1 Binding molecules and methods of use thereof BIOGEN MA INC. 2007-10-25 — — US disclosed
US-20070248988-A1 Binding molecules and methods of use thereof BIOGEN MA INC. 2007-10-25 — — US disclosed
US-20070093455-A1 10-substituted tetracyclines and methods of use thereof PARATEK PHARMACEUTICALS, INC. 2007-04-26 — — US disclosed
US-20070093455-A1 10-substituted tetracyclines and methods of use thereof PARATEK PHARMACEUTICALS, INC. 2007-04-26 — — US disclosed
WO-2006130431-A1 METHODS OF PURIFYING TIGECYCLINE WYETH (US) 2006-12-07 — — WO disclosed
US-6617318-B1 7-substitted tetracyclines are effective against tetracycline-resistant E. coli, S. aureus and E. faecalis strains TRUSTEES OF TUFTS COLLEGE 2003-09-09 — — 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 (10 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-20070093455-A1 10-substituted tetracyclines and methods of use thereof TET3, TET1, TMSB10 TDP1 1397/4885KDM4E 996/4885USP2 2844/4885
US-11129839-B2 Minocycline compounds for biodefense CD68, CD14, TREH TDP1 2875/4885KDM4E 3775/4885USP2 2225/4885
US-20180104262-A1 SALTS AND POLYMORPHS OF A TETRACYCLINE COMPOUND TPR, MALT1, TBCA TDP1 1583/4885KDM4E 4413/4885USP2 4310/4885
US-20070248988-A1 Binding molecules and methods of use thereof SHBG, CACYBP, CD2BP2 TDP1 1801/4885KDM4E 4410/4885USP2 3510/4885
US-20200330489-A1 MINOCYCLINE COMPOUNDS FOR BIODEFENSE CD68, CD14, TREH TDP1 2875/4885KDM4E 3775/4885USP2 2225/4885
US-20080287401-A1 Methods for Synthesizing and Purifying Aminoalkyl Tetracycline Compounds NPEPPS, AAAS, AADAC TDP1 1642/4885KDM4E 587/4885USP2 1688/4885
US-20210395189-A1 SUBSTITUTED TETRACYCLINE COMPOUNDS TET1, TET3, MYC TDP1 2522/4885KDM4E 1193/4885USP2 2300/4885
US-20240238315-A1 MINOCYCLINE COMPOUNDS FOR BIODEFENSE CD68, CD14, TREH TDP1 2875/4885KDM4E 3775/4885USP2 2225/4885
US-20180133231-A1 MINOCYCLINE COMPOUNDS FOR BIODEFENSE CD68, CD14, TREH TDP1 2875/4885KDM4E 3775/4885USP2 2225/4885
US-10252984-B2 Inhibiting G protein coupled receptor 6 kinase polypeptides GRK6, GRK2, GRK3 TDP1 3105/4885KDM4E 4504/4885USP2 2725/4885

“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.

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