Chloroform

Chloroform

SCHEMBL2819782

CCO.ClC(Cl)Cl.ClC(Cl)Cl

nearest known ligand 0.60

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

MMP1MMP13MMP7MMP8polrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
TSHR P16473 7/20 0.60
ALDH1A1 P00352 4/20 0.60
LMNA P02545 1/20 0.40
TDP1 Q9NUW8 2/20 0.35
TP53 P04637 1/20 0.35
CYP2C9 P11712 1/20 0.30

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
Chloroform SCHEMBL8192102 1.00 TSHR (0.60) TSHRALDH1A1LMNATDP1TP53
Chloroform SCHEMBL8927142 1.00 TSHR (0.60) TSHRALDH1A1LMNATDP1TP53
Chloroform SCHEMBL8196816 1.00 TSHR (0.60) TSHRALDH1A1LMNATDP1TP53
Chloroform SCHEMBL7542885 1.00 TSHR (0.60) TSHRALDH1A1LMNATDP1TP53
Chloroform SCHEMBL35119 1.00
Chloroform SCHEMBL7542887 1.00 TSHR (0.60) TSHRALDH1A1LMNATDP1TP53
Chloroform SCHEMBL7768433 1.00 TSHR (0.60) TSHRALDH1A1LMNATDP1TP53
Chloroform SCHEMBL8927139 1.00 TSHR (0.60) TSHRALDH1A1LMNATDP1TP53
Chloroform SCHEMBL2118727 0.95
Chloroform SCHEMBL6974119 0.95

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2220103-B1 NOVEL MANGIFERIN CALCIUM SALTS, THE METHOD FOR ITS PREPARATION AND ITS USE HAINAN DEZE DRUG RES CO LTD (CN) 2015-04-08 EP disclosed
US-8334267-B2 Mangiferin calcium salts, the method for its preparation and its use HAINAN DEZE DRUG RESEARCH CO., LTD. (CN) 2012-12-18 US disclosed
US-20100249046-A1 NOVEL MANGIFERIN CALCIUM SALTS, THE METHOD FOR ITS PREPARATION AND ITS USE CHANGZHOU DEZE MEDICAL SCIENCE CO., LTD (CN) 2010-09-30 US disclosed
EP-2220103-A1 NOVEL MANGIFERIN CALCIUM SALTS, THE METHOD FOR ITS PREPARATION AND ITS USE Hainan Deze Drug Research Co., Ltd (CN) 2010-08-25 EP disclosed
WO-2009065287-A1 NOVEL MANGIFERIN CALCIUM SALTS, THE METHOD FOR ITS PREPARATION AND ITS USE HAINAN DEZE DRUG RESEARCH CO., LTD (CN) 2009-05-28 WO disclosed
WO-2008061480-A1 NOVEL MANGIFERIN CALCIUM SALTS, THE METHOD FOR ITS PREPARATION AND ITS USE HAINAN DEZE DRUG RESEARCH CO., LTD (CN) 2008-05-29 WO disclosed
EP-0940387-B1 PHENYLETHANOLAMINE COMPOUNDS USEFUL AS BETA3 AGONIST, PROCESS FOR PRODUCING THE SAME, AND INTERMEDIATES IN THE PRODUCTION OF THE SAME MITSUBISHI PHARMA CORP (JP) 2003-05-07 EP disclosed
US-6069176-A PHENYLETHANOLAMINE COMPOUNDS WITH A BETA-3 ADRENERGIC RECEPTOR STIMULATING EFFECT, USE AS A THERAPY FOR URINARY INCONTINENCE MITSUBISHI-TOKYO PHARMACEUTICALS, INC. (JP) 2000-05-30 US disclosed
EP-0940387-A1 PHENYLETHANOLAMINE COMPOUNDS USEFUL AS BETA3 AGONIST, PROCESS FOR PRODUCING THE SAME, AND INTERMEDIATES IN THE PRODUCTION OF THE SAME TOKYO TANABE COMPANY LIMITED (JP) 1999-09-08 EP disclosed
US-5629419-A Process for preparing 4-mercaptopyrrolidine intermediate compounds and a process for their use in preparing carbapenem -2-em-3 carboxylic acids TANABE SEIYAKU CO., LTD. (JP) 1997-05-13 US disclosed
EP-0713866-A1 Process for preparing 4-mercaptopyrrolidine compound TANABE SEIYAKU CO., LTD. (JP) 1996-05-29 EP disclosed
US-5399703-A Antiallergens NIPPON SHINYAKU COMPANY, LIMITED (JP) 1995-03-21 US disclosed
EP-0308977-B1 Anthracycline derivatives having inhibitory activity against reverse transcriptase of human immunodeficiency virus ZAIDAN HOJIN BISEIBUTSU (JP) 1993-12-08 EP disclosed
EP-0536400-A1 TETRAZOLE DERIVATIVE AND MEDICINE NIPPON SHINYAKU COMPANY, LIMITED (JP) 1993-04-14 EP disclosed
US-5003055-A Anthracycline derivatives having inhibitory activity against reverse transcriptase of human immunodeficiency virus ZAIDAN HOJIN BISEIBUTSU KAGAKU KENKYU KAI (JP) 1991-03-26 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-20100249046-A1 NOVEL MANGIFERIN CALCIUM SALTS, THE METHOD FOR ITS PREPARATION AND ITS USE ORAI1, SARAF, ITPR3 TSHR 4024/4885ALDH1A1 4654/4885LMNA 726/4885

“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.