Prochlorperazine

Prochlorperazine

SCHEMBL1041250

CN1CCN(CCCN2c3ccccc3Sc3ccc(Cl)cc32)CC1.Cl

nearest known ligand 0.98

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

DRD2

The experimentally established mechanism targets of Prochlorperazine. 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 10/20 0.98
▸ MAPT P10636 8/20 0.98
▸ MAPK1 P28482 7/20 0.98
▸ LMNA P02545 7/20 0.98
▸ SMN1; SMN2 Q16637 7/20 0.98
▸ ADRA2A P08913 7/20 0.98
▸ ADRA2C P18825 7/20 0.98
▸ SLC6A2 P23975 7/20 0.98
▸ HTR2A P28223 7/20 0.98
▸ SLC6A4 P31645 7/20 0.98
▸ HRH1 P35367 7/20 0.98
▸ DRD3 P35462 7/20 0.98
▸ HTR1A P08908 7/20 0.98
▸ TP53 P04637 6/20 0.98
▸ CYP3A4 P08684 6/20 0.98
▸ ADRA1A P35348 6/20 0.98
▸ SLC6A3 Q01959 6/20 0.98
▸ KCNH2 Q12809 6/20 0.98
▸ CYP2D6 P10635 6/20 0.98
▸ ADRA2B P18089 6/20 0.98

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
Prochlorperazine SCHEMBL2506559 1.00 DRD2 (0.98) DRD2MAPTMAPK1LMNASMN1; SMN2
Prochlorperazine SCHEMBL18429 0.99 DRD2 (1.00) DRD2MAPTMAPK1LMNASMN1; SMN2
Prochlorperazine SCHEMBL29369439 0.99 DRD2 (1.00) DRD2MAPTMAPK1LMNASMN1; SMN2
Prochlorperazine SCHEMBL29358207 0.99 DRD2 (1.00) DRD2MAPTMAPK1LMNASMN1; SMN2
Prochlorperazine SCHEMBL14126977 0.99 DRD2 (1.00) DRD2MAPTMAPK1LMNASMN1; SMN2
Prochlorperazine SCHEMBL133595 0.98 DRD2 (0.98) DRD2MAPTMAPK1LMNASMN1; SMN2
Perphenazine SCHEMBL28086447 0.93 MAPT (0.91) DRD2MAPTMAPK1LMNASMN1; SMN2
Perphenazine SCHEMBL5307579 0.93 MAPT (0.91) DRD2MAPTMAPK1LMNASMN1; SMN2
Prochlorperazine SCHEMBL10891828 0.92 MAPT (0.90) DRD2MAPTMAPK1LMNASMN1; SMN2
SCHEMBL13485632 0.92 MAPT (0.86) DRD2MAPTMAPK1LMNASMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6121276-A ORALLY ADMINISTERING DSAGE OF APOMORPHINE TOGETHER WITH ANTIEMETIC PRIOR TO INTERCOURSE; SIDE EFFECT REDUCTION PENTECH PHARMACEUTICALS, INC. (US) 2000-09-19 — — US claimed
CN-116507327-A Chewable formulations 礼蓝动物保健有限公司 2023-07-28 — — CN disclosed
CN-114846012-A 2-isoindole-1, 3, 4-oxadiazole derivatives useful as HDAC6 inhibitors 武田药品工业株式会社 2022-08-02 — — CN disclosed
US-11033510-B2 Anti-inflammatory pharmaceutical compositions and methods of administration LANCE L. GOOBERMAN (US) 2021-06-15 — — US disclosed
CN-112955124-A Oral film compositions and dosage forms having precise active dissolution profiles 阿奎蒂夫疗法公司 2021-06-11 — — CN disclosed
CN-112585690-A System and method for producing individualized individual unit doses containing a pharmaceutically active substance 阿奎斯蒂弗医疗股份有限公司 2021-03-30 — — CN disclosed
CN-112384223-A Pharmaceutical composition containing poorly soluble basic drug 中外制药株式会社 2021-02-19 — — CN disclosed
CN-212167407-U Compounding device is used in production of hydrochloric acid lorcyclizine 焦作福瑞堂制药有限公司 2020-12-18 — — CN disclosed
EP-3095442-B1 INJECTABLE SUSPENSIONS HAVING IMPROVED INJECTABILITY PROPERTIES ALKERMES CONTROLLED THERAPEUTICS INC (US) 2020-11-18 — — EP disclosed
CN-211936518-U Refining plant of hydrochloric acid lorcyclizine production usefulness 焦作福瑞堂制药有限公司 2020-11-17 — — CN disclosed
US-6284283-B1 ATOMIZING USING MULTIFLUID ATOMIZATION DISPERSED SYSTEM COMPRISING BIOLOGICALLY ACTIVE AGENT AND SOLVENT TO PRODUCE DROPLETS; FREEZING; REMOVING SOLVENT FROM FROZEN DROPLETS TO PRODUCE FRIABLE MICROSTRUCTURES; DISPERSION; FRAGMENTING ALKERMES CONTROLLED THERAPEUTICS, INC. 2001-09-04 — — US disclosed
WO-2001058428-A1 METHOD OF PREPARING A SUSTAINED RELEASE COMPOSITION ALKERMES CONTROLLED THERAPEUTICS, INC. (US) 2001-08-16 — — WO disclosed
US-6264987-B1 MIXING; CONTROLLING TEMPERATURE ALKERMES CONTROLLED THERAPEUTICS INC. II 2001-07-24 — — US disclosed
EP-1094799-A1 APOMORPHINE-CONTAINING DOSAGE FORMS FOR AMELIORATING MALE ERECTILE DYSFUNCTION PENTECH PHARMACEUTICALS, INC. (US) 2001-05-02 — — EP disclosed
WO-2001028525-A2 METHOD OF PRODUCING SUB-MICRON PARTICLES OF BIOLOGICALLY ACTIVE AGENTS ALKERMES CONTROLLED THERAPEUTICS, INC. (US) 2001-04-26 — — WO disclosed
US-6121276-A ORALLY ADMINISTERING DSAGE OF APOMORPHINE TOGETHER WITH ANTIEMETIC PRIOR TO INTERCOURSE; SIDE EFFECT REDUCTION PENTECH PHARMACEUTICALS, INC. (US) 2000-09-19 — — US disclosed
WO-1999066916-A1 APOMORPHINE-CONTAINING DOSAGE FORMS FOR AMELIORATING MALE ERECTILE DYSFUNCTION PENTECH PHARMACEUTICALS, INC. (US) 1999-12-29 — — WO disclosed
US-5989463-A FORMING SOLID PARTICLE MATRIX BY ATOMIZING/DESOLVENTIZING A CONTINUOUS PHASE IN WHICH A POLYMER AND A BIOACTIVE MATERIAL, I.E, DRUG, ARE BOTH DISSOLVED ALKERMES CONTROLLED THERAPEUTICS, INC. (US) 1999-11-23 — — US disclosed
US-5804218-A ORALLY ADMINISTERING INSOLUBLE ZINC SALT TO ADSORB SOLUBLE BILIRUBIN IN GASTROINTESTINAL TRACT BRIGHAM & WOMEN'S HOSPITAL, INC. (US) 1998-09-08 — — US disclosed
WO-1998007412-A1 CONTROLLED RELEASE MICROPARTICLES WITH A HYDROPHOBIC MATERIAL ALKERMES CONTROLLED THERAPEUTICS, INC. (US) 1998-02-26 — — WO disclosed
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