Chlortetracycline

Chlortetracycline

SCHEMBL16726392

CN(C)[C@@H]1C(O)=C(C(N)=O)C(=O)[C@@]2(O)C(O)=C3C(=O)c4c(O)ccc(Cl)c4C(C)(O)[C@H]3C[C@@H]12

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 SCHEMBL3110 1.00 MAPT (0.71) MAPTHSD17B10GAALMNAPOLB
Chlortetracycline SCHEMBL27323552 1.00 MAPT (0.71) MAPTHSD17B10GAALMNAPOLB
Chlortetracycline SCHEMBL5503038 1.00 MAPT (0.71) MAPTHSD17B10GAALMNAPOLB
Chlortetracycline SCHEMBL10901448 1.00 MAPT (0.71) MAPTHSD17B10GAALMNAPOLB
Chlortetracycline SCHEMBL12356689 1.00 MAPT (0.71) MAPTHSD17B10GAALMNAPOLB
Chlortetracycline SCHEMBL13782583 1.00 MAPT (0.71) MAPTHSD17B10GAALMNAPOLB
Chlortetracycline SCHEMBL13782533 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 3 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20180016225-A1 TETRACYCLINE COMPOUNDS HAVING TARGET THERAPEUTIC ACTIVITIES PARATEK PHARMACEUTICALS, INC. 2018-01-18 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

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 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-20180016225-A1 TETRACYCLINE COMPOUNDS HAVING TARGET THERAPEUTIC ACTIVITIES TBCA, TUBB6, TUBB MAPT 823/4885HSD17B10 1112/4885GAA 41/4885
US-20150141381-A1 TETRACYCLINE COMPOUNDS HAVING TARGET THERAPEUTIC ACTIVITIES TBCA, TUBB6, TUBB MAPT 823/4885HSD17B10 1112/4885GAA 41/4885

“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.