Chlorprothixene

Chlorprothixene

SCHEMBL24133

CN(C)CC/C=C1\c2ccccc2Sc2ccc(Cl)cc21

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

DRD2DRD3HTR2AHTR2C

The experimentally established mechanism targets of Chlorprothixene. 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
DRD2 known ✓ P14416 4/20 1.00
DRD3 known ✓ P35462 4/20 1.00
HTR2A known ✓ P28223 2/20 0.58
HTR2C known ✓ P28335 2/20 0.58
LMNA P02545 5/20 1.00
CYP3A4 P08684 4/20 1.00
CYP2D6 P10635 4/20 1.00
HRH1 P35367 4/20 1.00
CYP1A2 P05177 3/20 1.00
CYP2C19 P33261 3/20 1.00
ADRA2A P08913 3/20 1.00
SLC6A2 P23975 3/20 1.00
SLC6A4 P31645 3/20 1.00
ADRA1A P35348 3/20 1.00
SLC6A3 Q01959 3/20 1.00
KCNH2 Q12809 3/20 1.00
TDP1 Q9NUW8 2/20 1.00
HTR1A P08908 2/20 1.00
HTR6 P50406 2/20 1.00
CHRM2 P08172 2/20 1.00

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
Chlorprothixene SCHEMBL30383335 1.00 LMNA (1.00) LMNACYP3A4CYP2D6DRD2HRH1
Chlorprothixene SCHEMBL94235 1.00 LMNA (1.00) LMNACYP3A4CYP2D6DRD2HRH1
Chlorprothixene SCHEMBL29626798 1.00 LMNA (1.00) LMNACYP3A4CYP2D6DRD2HRH1
Chlorprothixene SCHEMBL94236 1.00 LMNA (1.00) LMNACYP3A4CYP2D6DRD2HRH1
Chlorprothixene SCHEMBL29357955 1.00 LMNA (1.00) LMNACYP3A4CYP2D6DRD2HRH1
Chlorprothixene SCHEMBL455759 0.99 LMNA (1.00) LMNACYP3A4CYP2D6DRD2HRH1
Chlorprothixene SCHEMBL29857011 0.99 LMNA (1.00) LMNACYP3A4CYP2D6DRD2HRH1
Chlorprothixene SCHEMBL455758 0.99 LMNA (1.00) LMNACYP3A4CYP2D6DRD2HRH1
Chlorprothixene SCHEMBL3491182 0.92 LMNA (0.84) LMNACYP3A4CYP2D6DRD2HRH1
Chlorprothixene SCHEMBL29462906 0.90 LMNA (0.84) LMNACYP3A4CYP2D6DRD2HRH1

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 1918 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250152591-A1 TREATMENT OF HEMATOLOGICAL MALIGNANCIES WITH MENIN INHIBITORS AND P-GLYCOPROTEIN INHIBITORS KURA ONCOLOGY INC (US) 2025-05-15 US claimed
EP-4472637-A1 TREATMENT OF HEMATOLOGICAL MALIGNANCIES WITH MENIN INHIBITORS AND P-GLYCOPROTEIN INHIBITORS Kura Oncology, Inc. (US) 2024-12-11 EP claimed
WO-2023150635-A1 TREATMENT OF HEMATOLOGICAL MALIGNANCIES WITH MENIN INHIBITORS AND P-GLYCOPROTEIN INHIBITORS KURA ONCOLOGY, INC. (US) 2023-08-10 WO claimed
EP-1931320-B1 MICROPARTICLES WITH MODIFIED RELEASE OF AT LEAST ONE ACTIVE PRINCIPLE AND ORAL DOSAGE FORM COMPRISING THE SAME FLAMEL IRELAND LTD (IE) 2022-06-15 EP claimed
US-20220050117-A1 GLX-DERIVED MOLECULE DETECTION GLX ANALYTIX APS (DK) 2022-02-17 US claimed
CN-108593828-A Blood plasma prepares the detection method of drug and toxic content in card 李水军 2018-09-28 CN claimed
CN-107088191-A The new application of medicine taractan 深圳市坤健创新药物研究院 2017-08-25 CN claimed
CN-106456662-A Compositions of pentosan polysulfate for oral administration and methods of use thereof 奥利金制药公司 2017-02-22 CN claimed
CN-104965035-B Method for screening toxic substances in sample by using solid phase support liquid-liquid extraction-GC MS 公安部物证鉴定中心 2017-02-01 CN claimed
CN-104965035-A Method for screening toxic substances in sample by using solid phase support liquid-liquid extraction-GC MS INST FORENSIC SCIENCE MINISTRY PUBLIC SECURITY PRC 2015-10-07 CN claimed
JP-2000516204-A 2000-12-05 JP claimed
EP-0954327-A1 USEFUL FORMULATIONS OF ACID ADDITION SALT DRUGS OXIGENE, INC. (US) 1999-11-10 EP claimed
WO-1999025353-A1 THERAPEUTIC USES OF TRIAZOLO-PYRIDAZINE DERIVATIVES MERCK SHARP & DOHME LIMITED (GB) 1999-05-27 WO claimed
WO-1998000159-A1 USEFUL FORMULATIONS OF ACID ADDITION SALT DRUGS OXIGENE, INC. (US) 1998-01-08 WO claimed
WO-1994023726-A1 CALMODULIN BLOCKING AGENT ADDUCTS USEFUL AS ANTI-PLATELET AGENTS MALLINCKRODT MEDICAL, INC. (US) 1994-10-27 WO claimed
CN-1093934-A Protective sheath for pasting and moxibustion CHEN JIE (CN) 1994-10-26 CN claimed
EP-0174342-B1 BRAIN-SPECIFIC ANALOGUES OF CENTRALLY ACTING AMINES UNIVERSITY OF FLORIDA (US) 1989-12-20 EP claimed
EP-0126848-B1 SUSPENSION AGENT MIXTURE AS AN ADDITIVE TO CALCIUM SULPHATE HEMI-HYDRATE FOR THE MANUFACTURE OF MOULDS Börgardts-Sachsenstein GmbH (DE) 1987-12-09 EP claimed
EP-0152379-A2 Process for preparing pharmaceutical compositions containing unilamellar liposomes CIBA-GEIGY AG (CH) 1985-08-21 EP claimed
US-4377577-A Use of psychoactive drugs in uterus to prevent pregnancy UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. (US) 1983-03-22 US claimed

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-20250152591-A1 TREATMENT OF HEMATOLOGICAL MALIGNANCIES WITH MENIN INHIBITORS AND P-GLYCOPROTEIN INHIBITORS MEN1, ABCB1, ABCC1 DRD2 4691/4885DRD3 4667/4885HTR2A 2880/4885

“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.