Chloramphenicol

Chloramphenicol

SCHEMBL4295048

O=C(N[C@H](CO)[C@@H](O)c1ccc([N+](=O)[O-])cc1)C(Cl)Cl

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

rplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Chloramphenicol. 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
LMNA P02545 4/20 1.00
CYP3A4 P08684 3/20 1.00
TSHR P16473 2/20 1.00
SMN1; SMN2 Q16637 1/20 1.00
ALDH1A1 P00352 1/20 1.00
MARS2 Q96GW9 1/20 1.00
CYP2C19 P33261 1/20 1.00
RPLP1 P05386 1/20 0.90
RPLP0 P05388 1/20 0.90
RPS17 P08708 1/20 0.90
RPSA P08865 1/20 0.90
RPS2 P15880 1/20 0.90
RPL35A P18077 1/20 0.90
RPL7 P18124 1/20 0.90
RPL17 P18621 1/20 0.90
RPS4Y1 P22090 1/20 0.90
RPS3 P23396 1/20 0.90
RPS12 P25398 1/20 0.90
RPL13 P26373 1/20 0.90
RPL10 P27635 1/20 0.90

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
Chloramphenicol SCHEMBL4262903 1.00 LMNA (1.00) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL28181476 1.00 LMNA (1.00) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL49057 1.00 LMNA (1.00) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL16111 1.00 LMNA (1.00) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL29557257 1.00 LMNA (1.00) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL537158 1.00 LMNA (1.00) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL11131056 0.99 LMNA (0.97) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL41042 0.99 LMNA (0.97) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL20531030 0.99 LMNA (0.97) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1
Chloramphenicol SCHEMBL28607485 0.99 LMNA (0.97) LMNACYP3A4TSHRSMN1; SMN2ALDH1A1

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 1 patent. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20090209615-A1 INHIBITORS OF MATRIX METALLOPROTEINASES TO TREAT NEUROLOGICAL DISORDERS NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2009-08-20 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 (1 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-20090209615-A1 INHIBITORS OF MATRIX METALLOPROTEINASES TO TREAT NEUROLOGICAL DISORDERS MMP9, MMP10, MMP17 LMNA 1476/4885CYP3A4 3597/4885TSHR 4174/4885

“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.