Prolonium

Prolonium

SCHEMBL2889745

C[N+](C)(C)CC(O)C[N+](C)(C)C.[Cl-].[Cl-]

nearest known ligand 0.57

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEBDKRB2CHRM1CHRM2CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNGGUCY1A1GUCY1A2GUCY1B1GUCY1B2NAMPTPTAFRSLC10A2SLC6A2SLC6A3TACR1dacAdacBdacCftsImrcAmrcBmrdA

The experimentally established mechanism targets of Prolonium. 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
CHRM2 known ✓ P08172 2/20 0.36
CHRM1 known ✓ P11229 2/20 0.36
CHRM3 known ✓ P20309 1/20 0.35
MAPT P10636 3/20 0.57
SLC22A16 Q86VW1 1/20 0.50
SMN1; SMN2 Q16637 2/20 0.40
GALR3 O60755 1/20 0.40
BLM P54132 1/20 0.40
LMNA P02545 5/20 0.39
CYP3A4 P08684 1/20 0.37
SLC5A7 Q9GZV3 1/20 0.37
TSHR P16473 2/20 0.36
CHRM4 P08173 2/20 0.36
TBXA2R P21731 1/20 0.36
CPT2 P23786 1/20 0.35
CPT1A P50416 1/20 0.35
CHRM5 P08912 1/20 0.35
CYP2C9 P11712 1/20 0.35
APEX1 P27695 2/20 0.33
ALDH1A1 P00352 1/20 0.33

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
Prolonium SCHEMBL1649967 0.96 MAPT (0.52) MAPTSLC22A16SMN1; SMN2GALR3BLM
SCHEMBL13380702 0.93 MAPT (0.52) MAPTSLC22A16SMN1; SMN2GALR3BLM
Prolonium SCHEMBL1650849 0.92 MAPT (0.50) MAPTSLC22A16SMN1; SMN2GALR3BLM
Prolonium SCHEMBL5705670 0.92 MAPT (0.50) MAPTSLC22A16SMN1; SMN2GALR3BLM
Prolonium SCHEMBL11723705 0.92 MAPT (0.50) MAPTSLC22A16SMN1; SMN2GALR3BLM
Hydrochloric Acid SCHEMBL9819532 0.83 MAPT (0.50) MAPTSLC22A16SMN1; SMN2GALR3BLM
Hydrochloric Acid SCHEMBL35525 0.83 MAPT (0.50) MAPTSLC22A16SMN1; SMN2GALR3BLM
SCHEMBL16405718 0.83 MAPT (0.44) MAPTSLC22A16SMN1; SMN2GALR3BLM
Hydrochloric Acid SCHEMBL28705517 0.81
Hydrochloric Acid SCHEMBL872025 0.81 MAPT (0.48) MAPTSLC22A16SMN1; SMN2GALR3BLM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9688905-B2 Methods for enhancing propped fracture conductivity HALLIBURTON ENERGY SERVICES, INC. (US) 2017-06-27 US claimed
US-20160053160-A1 METHODS FOR ENHANCING PROPPED FRACTURE CONDUCTIVITY HALLIBURTON ENERGY SERVICES, INC. 2016-02-25 US claimed
WO-2015069293-A1 METHODS FOR ENHANCING PROPPED FRACTURE CONDUCTIVITY HALLIBURTON ENERGY SERVICES, INC. (US) 2015-05-14 WO claimed
US-20040235677-A1 Methods and compositions for stabilizing swelling clays or migrating fines in formations HALLIBURTON ENERGY SERVICES, INC. 2004-11-25 US claimed
US-5145558-A Optical brightener THE DOW CHEMICAL COMPANY (US) 1992-09-08 US claimed
EP-0429241-A1 Process for alkaline peroxide bleaching of wood pulp using a quaternary amine as additive THE DOW CHEMICAL COMPANY (US) 1991-05-29 EP claimed
US-5013404-A Paper with improved brightness THE DOW CHEMICAL COMPANY (US) 1991-05-07 US claimed
JP-59129218-A None JP disclosed
JP-59129216-A None JP disclosed
JP-59129217-A None JP disclosed
US-9688905-B2 Methods for enhancing propped fracture conductivity HALLIBURTON ENERGY SERVICES, INC. (US) 2017-06-27 US disclosed
EP-2010573-B1 CATIONIC POLYSACCHARIDE, ITS PREPARATION AND USE CHEMIGATE OY (FI) 2017-03-29 EP disclosed
EP-2192228-B1 USE OF CATIONIC STARCH CHEMIGATE OY (FI) 2017-03-29 EP disclosed
EP-0371823-A1 Crystalline 3-methacryloyloxy-2-hydroxypropyl-trimethylammonium chloride monomer POLYPURE INC. (US) 1990-06-06 EP disclosed
EP-0371821-A1 A process for the production of substituted acryloyloxyhydroxypropyltrialkylammonium chloride RHONE-POULENC SPECIALTY CHEMICALS CO. (US) 1990-06-06 EP disclosed
WO-1988000582-A1 METHOD OF PURIFYING 3-CHLORO-2-HYDROXYPROPYL TRIALKYLAMMONIUM CHLORIDE THE DOW CHEMICAL COMPANY (US) 1988-01-28 WO disclosed
US-4602110-A FORMING AQUEOUS SLURRY, PRECIPITATING WITH ALCOHOL THE DOW CHEMICAL COMPANY (US) 1986-07-22 US disclosed
JP-S59129218-A RENDERING POLYESTER (METH)ACRYLATE RESIN THIXOTROPIC NIPPON SHOKUBAI KAGAKU KOGYO CO LTD 1984-07-25 JP disclosed
JP-S59129216-A RENDERING POLY(METH)ACRYLATE RESIN THIXOTROPIC NIPPON SHOKUBAI KAGAKU KOGYO CO LTD 1984-07-25 JP disclosed
JP-S59129217-A RENDERING UNSATURATED POLYESTER RESIN THIXOTROPIC NIPPON SHOKUBAI KAGAKU KOGYO CO LTD 1984-07-25 JP disclosed