Trichlorethanol

Trichlorethanol

SCHEMBL762332

ClC(Cl)Cl.ClC(Cl)Cl.ClC(Cl)Cl.ClC(Cl)Cl.ClC(Cl)Cl.ClC(Cl)Cl.ClC(Cl)Cl.ClC(Cl)Cl.ClC(Cl)Cl.ClC(Cl)Cl.ClC(Cl)Cl.OCC(Cl)(Cl)Cl

nearest known ligand 0.33

Full drug profile on Sugi Atlas →

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.33
TDP1 Q9NUW8 2/20 0.32
TP53 P04637 1/20 0.32
TSHR P16473 1/20 0.32

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
Trichlorethanol SCHEMBL325071 1.00 LMNA (0.33) LMNATDP1TP53TSHR
Trichlorethanol SCHEMBL7261325 1.00 LMNA (0.33) LMNATDP1TP53TSHR
Trichlorethanol SCHEMBL291748 1.00 LMNA (0.33) LMNATDP1TP53TSHR
Trichlorethanol SCHEMBL759616 1.00 LMNA (0.33) LMNATDP1TP53TSHR
Trichlorethanol SCHEMBL1436780 1.00 LMNA (0.33) LMNATDP1TP53TSHR
Trichlorethanol SCHEMBL8522341 1.00 LMNA (0.33) LMNATDP1TP53TSHR
Trichlorethanol SCHEMBL16162174 1.00 LMNA (0.33) LMNATDP1TP53TSHR
Trichlorethanol SCHEMBL4450822 1.00 LMNA (0.33) LMNATDP1TP53TSHR
Trichlorethanol SCHEMBL88329 1.00 LMNA (0.33) LMNATDP1TP53TSHR
Trichlorethanol SCHEMBL6898269 1.00 LMNA (0.33) LMNATDP1TP53TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102772501-A Rheum emodi Wall. extract and its preparing method TIBET JINHADA PHARMACEUTICAL CO LTD 2012-11-14 CN claimed
CN-108137638-B Bridged nucleic acid GuNA, method for producing same, and intermediate compound 田边三菱制药株式会社 2022-05-03 CN disclosed
US-10961269-B2 Bridged nucleic acid GuNA, method for producing same, and intermediate compound MITSUBISHI TANABE PHARMA CORPORATION (JP) 2021-03-30 US disclosed
CN-108003119-B Method for synthesizing cabazitaxel from 10-deacetylbaccatin III 云南汉德生物技术有限公司 2020-04-24 CN disclosed
US-20180251488-A1 CROSSLINKED NUCLEIC ACID GUNA, METHOD FOR PRODUCING SAME, AND INTERMEDIATE COMPOUND MITSUBISHI TANABE PHARMA CORPORATION (JP) 2018-09-06 US disclosed
EP-3351548-A1 CROSSLINKED NUCLEIC ACID GUNA, METHOD FOR PRODUCING SAME, AND INTERMEDIATE COMPOUND Mitsubishi Tanabe Pharma Corporation (JP) 2018-07-25 EP disclosed
CN-108137638-A Bridging type nucleic acid GuNA, its manufacturing method and midbody compound 田边三菱制药株式会社 2018-06-08 CN disclosed
CN-108047749-A Colored resin composition, color filter, liquid crystal display device, and organic E L display device 三菱化学株式会社 2018-05-18 CN disclosed
CN-103430099-B colored resin composition, color filter, liquid crystal display device, and organic E L display device 三菱化学株式会社 2018-02-13 CN disclosed
EP-2374802-B1 KYNURENINE PRODUCTION INHIBITOR KYOWA HAKKO KIRIN CO LTD (JP) 2014-04-23 EP disclosed
CN-1423635-A Nitrogenous compounds and antiviral drugs containing the same KUREHA CHEMICAL IND CO LTD (JP) 2003-06-11 CN disclosed
EP-1273571-A1 NITROGENOUS COMPOUNDS AND ANTIVIRAL DRUGS CONTAINING THE SAME Kureha Chemical Industry Co., Ltd. (JP) 2003-01-08 EP disclosed
CN-1093124-C Substituted 4-hydroxy-phenylalcanoic acid derivatives with activity to ppar-'gamma' GLAXO GROUP LTD (GB) 2002-10-23 CN disclosed
EP-0863141-B1 SUBSTITUTED HETEROAROMATIC DERIVATIVES BANYU PHARMA CO LTD (JP) 2001-09-12 EP disclosed
US-6130232-A Substituted piperidine derivatives as muscarinic M3 receptor antagonists BANYU PHARMACEUTICAL COALTD (JP) 2000-10-10 US disclosed
CN-1218460-A Substituted 4-hydroxy-phenylalcanoic acid derivatives with activity to ppar-'gamma' GLAXO GROUP LTD (GB) 1999-06-02 CN disclosed
CN-1211244-A Radicicol derivatives KYOWA HAKKO KOGYO KK (JP) 1999-03-17 CN disclosed
EP-0863141-A1 SUBSTITUTED HETEROAROMATIC DERIVATIVES BANYU PHARMACEUTICAL CO., LTD. (JP) 1998-09-09 EP disclosed
EP-0161436-B1 REDOX INDICATORS Roche Diagnostics GmbH (DE) 1987-09-02 EP disclosed
EP-0161436-A1 Redox indicators Roche Diagnostics GmbH (DE) 1985-11-21 EP 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-10961269-B2 Bridged nucleic acid GuNA, method for producing same, and intermediate compound POLRMT, POLM, NSUN2 LMNA 445/4885TDP1 150/4885TP53 862/4885
US-20180251488-A1 CROSSLINKED NUCLEIC ACID GUNA, METHOD FOR PRODUCING SAME, AND INTERMEDIATE COMPOUND NSUN2, RNMT, POLRMT LMNA 665/4885TDP1 190/4885TP53 1084/4885

“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.