SCHEMBL148356

SCHEMBL148356

CCCCC(CC)CC(CCC)P(=O)([O-])[O-].CCCCC(CC)CC(CCC)P(=O)([O-])[O-].CCCCC(CC)CC(CCC)P(=O)([O-])[O-].[Nd+3].[Nd+3]

nearest known ligand 0.46

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
CYP3A4 P08684 5/20 0.46
L3MBTL1 Q9Y468 1/20 0.46
CA2 P00918 4/20 0.42
ALDH1A1 P00352 5/20 0.41
TDP1 Q9NUW8 2/20 0.41
TSHR P16473 5/20 0.39
FDPS P14324 1/20 0.35
ATM Q13315 1/20 0.35
SMN1; SMN2 Q16637 2/20 0.34
LMNA P02545 1/20 0.34
POLB P06746 1/20 0.34
MAPK1 P28482 1/20 0.34
HTT P42858 1/20 0.34
GGPS1 O95749 2/20 0.33
TRPM8 Q7Z2W7 1/20 0.31

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
SCHEMBL673475 0.96 CYP3A4 (0.46) CYP3A4L3MBTL1CA2ALDH1A1TDP1
SCHEMBL672801 0.96 CYP3A4 (0.46) CYP3A4L3MBTL1CA2ALDH1A1TDP1
SCHEMBL639159 0.96 CYP3A4 (0.46) CYP3A4L3MBTL1CA2ALDH1A1TDP1
SCHEMBL2775263 0.79 FDPS (0.50) CYP3A4L3MBTL1CA2ALDH1A1TDP1
SCHEMBL7873954 0.78 FDPS (0.41) CYP3A4L3MBTL1CA2ALDH1A1TDP1
SCHEMBL27241159 0.77 CYP3A4 (0.42) CYP3A4L3MBTL1CA2ALDH1A1TDP1
Phosphoric Acid SCHEMBL28078858 0.76 ALDH1A1 (0.52) CYP3A4L3MBTL1CA2ALDH1A1TDP1
SCHEMBL154360 0.75 CYP3A4 (0.50) CYP3A4L3MBTL1CA2ALDH1A1TDP1
SCHEMBL152404 0.75 CYP3A4 (0.50) CYP3A4L3MBTL1CA2ALDH1A1TDP1
SCHEMBL29817522 0.75 CYP3A4 (0.50) CYP3A4L3MBTL1CA2ALDH1A1TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260035494-A1 METHOD FOR COLD FLOW REDUCTION OF ELASTOMERS GOODYEAR TIRE & RUBBER (US) 2026-02-05 US disclosed
US-20260001974-A1 DISULFUR DICHLORIDE AND SILANE/SILOXANE ADDITIVE FOR MOONEY JUMP GOODYEAR TIRE & RUBBER (US) 2026-01-01 US disclosed
US-20260002005-A1 DISULFUR DICHLORIDE AND ALKENYL ETHERS ADDITIVES FOR MOONEY JUMP GOODYEAR TIRE & RUBBER (US) 2026-01-01 US disclosed
US-12371516-B2 Aged lanthanide-based catalyst systems and their use in the preparation of cis-1,4-polydienes BRIDGESTONE CORPORATION (JP) 2025-07-29 US disclosed
US-20230183399-A1 AGED LANTHANIDE-BASED CATALYST SYSTEMS AND THEIR USE IN THE PREPARATION OF CIS-1,4-POLYDIENES BRIDGESTONE CORPORATION (JP) 2023-06-15 US disclosed
US-10590208-B2 Polymers functionalized with imine compounds containing a cyano group BRIDGESTONE CORPORATION (JP) 2020-03-17 US disclosed
US-9469706-B2 Polymers functionalized with unsaturated heterocycles containing a protected amino group BRIDGESTONE CORPORATION (JP) 2016-10-18 US disclosed
US-9458270-B2 Method for producing polydienes and polydiene copolymers with reduced cold flow BRIDGESTONE CORPORATION (JP) 2016-10-04 US disclosed
US-9447213-B2 Polymers functionalized with polycyano compounds BRIDGESTONE CORPORATION (JP) 2016-09-20 US disclosed
US-20160237179-A1 Polymers Functionalized With Imine Compounds Containing A Cyano Group BRIDGESTONE CORPORATION (JP) 2016-08-18 US disclosed
US-20110144282-A1 POLYMERS FUNCTIONALIZED WITH IMIDE COMPOUNDS CONTAINING A PROTECTED AMINO GROUP BRIDGESTONE CORPORATION (JP) 2011-06-16 US disclosed
US-7902309-B2 Process and catalyst system for polydiene production BRIDGESTONE CORPORATION (JP) 2011-03-08 US disclosed
US-20100317818-A1 POLYMERS FUNCTIONALIZED WITH HALOSILANES CONTAINING AN AMINO GROUP BRIDGESTONE CORPORATION (JP) 2010-12-16 US disclosed
US-20100216956-A1 PROCESS AND CATALYST SYSTEM FOR POLYDIENE PRODUCTION BRIDGESTONE CORPORATION (JP) 2010-08-26 US disclosed
US-20100168378-A1 POLYMERS FUNCTIONALIZED WITH NITROSO COMPOUNDS BRIDGESTONE CORPORATION (JP) 2010-07-01 US disclosed
US-7741418-B2 Process for producing polydienes BRIDGESTONE CORPORATION (JP) 2010-06-22 US disclosed
US-20100137520-A1 Branched Polymers and Methods for Their Synthesis and Use BRIDGESTONE CORPORATION (JP) 2010-06-03 US disclosed
US-20090171046-A1 PROCESS FOR PRODUCING POLYDIENES BRIDGESTONE CORPORATION (JP) 2009-07-02 US disclosed
US-20090171035-A1 POLYMERS FUNCTIONALIZED WITH POLYIMINE COMPOUNDS BRIDGESTONE CORPORATION (JP) 2009-07-02 US disclosed
US-20090099325-A1 POLYMERS FUNCTIONALIZED WITH HETEROCYCLIC NITRILE COMPOUNDS BRIDGESTONE CORPORATION 2009-04-16 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 (5 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-20260035494-A1 METHOD FOR COLD FLOW REDUCTION OF ELASTOMERS ITGA1, HSPA1A, SHC1 CYP3A4 1754/4885L3MBTL1 709/4885CA2 2428/4885
US-20110144282-A1 POLYMERS FUNCTIONALIZED WITH IMIDE COMPOUNDS CONTAINING A PROTECTED AMINO GROUP PARG, PIN1, NPEPPS CYP3A4 3282/4885L3MBTL1 4004/4885CA2 3856/4885
US-20260001974-A1 DISULFUR DICHLORIDE AND SILANE/SILOXANE ADDITIVE FOR MOONEY JUMP DCLRE1A, DDR1, FDFT1 CYP3A4 3059/4885L3MBTL1 1317/4885CA2 2748/4885
US-20260002005-A1 DISULFUR DICHLORIDE AND ALKENYL ETHERS ADDITIVES FOR MOONEY JUMP MRE11, DDR1, DDB1 CYP3A4 3475/4885L3MBTL1 613/4885CA2 2684/4885
US-20100317818-A1 POLYMERS FUNCTIONALIZED WITH HALOSILANES CONTAINING AN AMINO GROUP MSN, PARG, ALG1 CYP3A4 3873/4885L3MBTL1 2899/4885CA2 3404/4885

“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.