SCHEMBL172615

SCHEMBL172615

Cc1ccc(Oc2ccccc2C)cc1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR2A P28223 2/20 0.55
SLC6A4 P31645 2/20 0.55
SMN1; SMN2 Q16637 3/20 0.54
ALDH1A1 P00352 3/20 0.54
CYP1A2 P05177 1/20 0.54
CYP2C9 P11712 1/20 0.54
HPGD P15428 1/20 0.54
CYP2C19 P33261 1/20 0.54
LMNA P02545 1/20 0.53
HTT P42858 2/20 0.52
MAPK1 P28482 1/20 0.52
L3MBTL1 Q9Y468 1/20 0.52
MEN1 O00255 2/20 0.52
KMT2A Q03164 2/20 0.52
NPC1 O15118 1/20 0.52
TSHR P16473 1/20 0.52
RAB9A P51151 1/20 0.52
AR P10275 3/20 0.49
DRD2 P14416 1/20 0.49
DRD4 P21917 1/20 0.49

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
SCHEMBL28604976 0.98 HTR2A (0.53) HTR2ASLC6A4SMN1; SMN2ALDH1A1CYP1A2
SCHEMBL7690257 0.93 ALDH1A1 (0.59) HTR2ASLC6A4SMN1; SMN2ALDH1A1CYP1A2
SCHEMBL2608310 0.88 HTT (0.65) HTR2ASLC6A4SMN1; SMN2ALDH1A1CYP1A2
SCHEMBL28816731 0.86 LTA4H (0.55) SLC6A4SMN1; SMN2ALDH1A1CYP1A2CYP2C9
SCHEMBL232763 0.86 SMN1; SMN2 (0.56) SLC6A4SMN1; SMN2ALDH1A1CYP1A2CYP2C9
SCHEMBL16621785 0.86 HTT (0.70) HTR2ASLC6A4SMN1; SMN2ALDH1A1CYP1A2
SCHEMBL2321472 0.84 ALDH1A1 (0.61) SLC6A4SMN1; SMN2ALDH1A1CYP1A2CYP2C9
SCHEMBL3755350 0.84 ALDH1A1 (0.53) SLC6A4SMN1; SMN2ALDH1A1CYP1A2CYP2C9
SCHEMBL11853567 0.84 FFAR1 (0.53) HTR2ASLC6A4SMN1; SMN2ALDH1A1LMNA
Ammonia Solution, Strong SCHEMBL6579940 0.84 SMN1; SMN2 (0.54) SLC6A4SMN1; SMN2ALDH1A1CYP1A2CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12275695-B2 Fluid catalytic cracking of p-cresol dimer into phenolic monomers and process thereof COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2025-04-15 US claimed
US-20230202953-A1 FLUID CATALYTIC CRACKING OF P-CRESOL DIMER INTO PHENOLIC MONOMERS AND PROCESS THEREOF COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2023-06-29 US claimed
EP-0235647-B1 PROCESS FOR THE MANUFACTURE OF 6,13-DIHYDROQUINACRIDONES AND QUINACRIDONES BAYER AG (DE) 1993-09-29 EP claimed
US-4812568-A Process for the preparation of 6,13-dihydroquinacridones and quinacridones BAYER AKTIENGESELLSCHAFT (DE) 1989-03-14 US claimed
EP-0235647-A2 Process for the manufacture of 6,13-dihydroquinacridones and quinacridones BAYER AG (DE) 1987-09-09 EP claimed
US-12275695-B2 Fluid catalytic cracking of p-cresol dimer into phenolic monomers and process thereof COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2025-04-15 US disclosed
WO-2024081943-A2 TRANSPORT PROPERTY MODULATION VIA SOLVENT SPECIFIC BEHAVIOR IN CROSSLINKED NON-AQUEOUS MEMBRANES UNIVERSITY OF VIRGINIA PATENT FOUNDATION (US) 2024-04-18 WO disclosed
US-20230202953-A1 FLUID CATALYTIC CRACKING OF P-CRESOL DIMER INTO PHENOLIC MONOMERS AND PROCESS THEREOF COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2023-06-29 US disclosed
US-20230202953-A1 FLUID CATALYTIC CRACKING OF P-CRESOL DIMER INTO PHENOLIC MONOMERS AND PROCESS THEREOF COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2023-06-29 US disclosed
US-20230202953-A1 FLUID CATALYTIC CRACKING OF P-CRESOL DIMER INTO PHENOLIC MONOMERS AND PROCESS THEREOF COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2023-06-29 US disclosed
EP-3326715-B1 OXALIC ACID MONOAMIDE LIGAND, AND USES THEREOF IN COUPLING REACTION OF COPPER-CATALYZED ARYL HALOGEN SUBSTITUTE CE PHARM CO LTD (CN) 2021-09-15 EP disclosed
CN-109212059-A A kind of detection method of automobile leather odour component 上海应用技术大学 2019-01-15 CN disclosed
WO-2003007954-A2 SULFONYL ARYL HYDROXAMATES AND THEIR USE AS MATRIX METALLOPROTEASE INHIBITORS PHARMACIA CORPORATION (US) 2003-01-30 WO disclosed
US-6281386-B1 EXTRACTION; CONTERCURRENT WASHING ATOFINA (FR) 2001-08-28 US disclosed
US-4812568-A Process for the preparation of 6,13-dihydroquinacridones and quinacridones BAYER AKTIENGESELLSCHAFT (DE) 1989-03-14 US disclosed
US-4410869-A ISOMERIC MIXTURE OF DITOLYL ETHERS BAYER AKTIENGESELLSCHAFT (DE) 1983-10-18 US disclosed
EP-0045423-A1 Process for the alpha-halogenation of possibly substituted methyl aromatics BAYER AG (DE) 1982-02-10 EP disclosed
EP-0008735-A1 Process for the preparation of diphenyl ether carboxylic acids BAYER AG (DE) 1980-03-19 EP disclosed
US-4098816-A HYPOGLYCEMIC AGENTS AND ANTILIPEMIC AGENTS BEECHAM GROUP LIMITED (GB) 1978-07-04 US disclosed
US-4042603-A SUBSTITUTED DIBENZOFURAN OR 9-FLUORENONE FROM A DIPHENYL ETHER OR BENZOPHENONE UBE INDUSTRIES, LTD. (JA) 1977-08-16 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 (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-20230202953-A1 FLUID CATALYTIC CRACKING OF P-CRESOL DIMER INTO PHENOLIC MONOMERS AND PROCESS THEREOF CAT, MCCC2, FOS HTR2A 1410/4885SLC6A4 3285/4885SMN1; SMN2 4413/4885
US-12275695-B2 Fluid catalytic cracking of p-cresol dimer into phenolic monomers and process thereof CAT, MCCC2, FOS HTR2A 1410/4885SLC6A4 3285/4885SMN1; SMN2 4413/4885

“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.