Chlortetracycline

Chlortetracycline

SCHEMBL5503038

CN(C)C1C(O)=C(C(N)=O)C(=O)C2(O)C(O)=C3C(=O)c4c(O)ccc(Cl)c4C(C)(O)C3CC12

nearest known ligand 0.71

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

rplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Chlortetracycline. 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
▸ MAPT P10636 5/20 0.71
▸ HSD17B10 Q99714 4/20 0.71
▸ GAA P10253 3/20 0.71
▸ LMNA P02545 3/20 0.71
▸ POLB P06746 3/20 0.71
▸ THRB P10828 2/20 0.71
▸ HIF1A Q16665 2/20 0.71
▸ PLA2G1B P04054 1/20 0.71
▸ ATG4B Q9Y4P1 1/20 0.71
▸ PDE4A P27815 1/20 0.71
▸ PADI4 Q9UM07 1/20 0.71
▸ MEN1 O00255 10/20 0.70
▸ KMT2A Q03164 10/20 0.70
▸ TDP1 Q9NUW8 7/20 0.70
▸ USP2 O75604 5/20 0.70
▸ ALDH1A1 P00352 3/20 0.70
▸ HPGD P15428 1/20 0.70
▸ KDM4E B2RXH2 6/20 0.54
▸ CYP3A4 P08684 1/20 0.54
▸ RECQL P46063 1/20 0.54

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
Chlortetracycline SCHEMBL19787489 1.00 MAPT (0.71) MAPTHSD17B10GAALMNAPOLB
Chlortetracycline SCHEMBL12356689 1.00 MAPT (0.71) MAPTHSD17B10GAALMNAPOLB
Chlortetracycline SCHEMBL27323552 1.00 MAPT (0.71) MAPTHSD17B10GAALMNAPOLB
Chlortetracycline SCHEMBL13782533 1.00 MAPT (0.71) MAPTHSD17B10GAALMNAPOLB
Chlortetracycline SCHEMBL16726392 1.00 MAPT (0.71) MAPTHSD17B10GAALMNAPOLB
Chlortetracycline SCHEMBL13782583 1.00 MAPT (0.71) MAPTHSD17B10GAALMNAPOLB
Chlortetracycline SCHEMBL3110 1.00 MAPT (0.71) MAPTHSD17B10GAALMNAPOLB
Chlortetracycline SCHEMBL10901448 1.00 MAPT (0.71) MAPTHSD17B10GAALMNAPOLB
Chlortetracycline SCHEMBL20952683 1.00 MAPT (0.71) MAPTHSD17B10GAALMNAPOLB
Chlortetracycline SCHEMBL3111 1.00 MAPT (0.71) MAPTHSD17B10GAALMNAPOLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20210395189-A1 SUBSTITUTED TETRACYCLINE COMPOUNDS PARATEK PHARMACEUTICALS, INC. 2021-12-23 — — US disclosed
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-20170305840-A1 SUBSTITUTED TETRACYCLINE COMPOUNDS PARATEK PHARM INNC (US) 2017-10-26 — — US disclosed
US-20170305840-A1 SUBSTITUTED TETRACYCLINE COMPOUNDS PARATEK PHARM INNC (US) 2017-10-26 — — US disclosed
US-20170283368-A1 METHODS FOR SYNTHESIZING SUBSTITUTED TETRACYCLINE COMPOUNDS PARATEK PHARMACEUTICALS, INC. 2017-10-05 — — US disclosed
US-20170283368-A1 METHODS FOR SYNTHESIZING SUBSTITUTED TETRACYCLINE COMPOUNDS PARATEK PHARMACEUTICALS, INC. 2017-10-05 — — 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-20020077276-A1 Compositions and methods for treating hemorrhagic virus infections and other disorders ANTIBODY SYSTEMS, INC. 2002-06-20 — — US disclosed
US-5098417-A Cellulosic wound dressing with an active agent ionically absorbed thereon RICOH KYOSAN, INC. (JP) 1992-03-24 — — US disclosed
EP-0395476-A2 Method and apparatus for the production of ionic cloths for use in ionic dressings RICOH KYOSAN INC. (JP) 1990-10-31 — — EP disclosed
EP-0338173-A1 Ionic dressing for topical administration of drugs to wounds and burns RICOH KYOSAN INC. (JP) 1989-10-25 — — EP disclosed
US-4684728-A Solubilizing biologically active compounds with reactive hydrogen atoms BAYER AKTIENGESELLSCHAFT (DE) 1987-08-04 — — US disclosed
EP-0014263-B1 METHOD OF IMPROVING THE SOLUBILITY OF BIOLOGICALLY ACTIVE AGENTS IN WATER AND IN LOWER ALIPHATIC ALCOHOLS, AND COMPOUNDS HAVING AN IMPROVED SOLUBILITY BAYER AG (DE) 1982-05-05 — — EP disclosed
US-4324799-A Fungicidal thioglycolic acid anilides, processes for their manufacture and pesticidal compositions containing them HOECHST AKTIENGESELLSCHAFT (DE) 1982-04-13 — — US disclosed
EP-0017772-A1 Method of improving the solubility of biologically active agents in water and in lower aliphatic alcohols, and compounds having an improved solubility BAYER AG (DE) 1980-10-29 — — EP disclosed
EP-0014263-A2 Method of improving the solubility of biologically active agents in water and in lower aliphatic alcohols, and compounds having an improved solubility BAYER AG (DE) 1980-08-20 — — EP disclosed
US-3980798-A Dichloromaleic imides for fungicidal composition and method CIBA-GEIGY CORPORATION (US) 1976-09-14 — — 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 (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-20020077276-A1 Compositions and methods for treating hemorrhagic virus infections and other disorders IL1R1, TNF, IL1A MAPT 1669/4885HSD17B10 3400/4885GAA 4525/4885
US-20190040001-A1 METHODS OF USING SUBSTITUTED TETRACYCLINE COMPOUNDS TO MODULATE RNA NSUN3, NSUN2, RNMT MAPT 3193/4885HSD17B10 2912/4885GAA 2673/4885
US-20170305840-A1 SUBSTITUTED TETRACYCLINE COMPOUNDS MYC, TET1, TET3 MAPT 1743/4885HSD17B10 1591/4885GAA 2782/4885
US-20210395189-A1 SUBSTITUTED TETRACYCLINE COMPOUNDS TET1, TET3, MYC MAPT 815/4885HSD17B10 2179/4885GAA 2998/4885
US-20180016225-A1 TETRACYCLINE COMPOUNDS HAVING TARGET THERAPEUTIC ACTIVITIES TBCA, TUBB6, TUBB MAPT 823/4885HSD17B10 1112/4885GAA 41/4885
US-20170283368-A1 METHODS FOR SYNTHESIZING SUBSTITUTED TETRACYCLINE COMPOUNDS TET3, TET1, DHFR MAPT 2181/4885HSD17B10 1786/4885GAA 679/4885

“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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