SCHEMBL6086949

SCHEMBL6086949

CC(C)C1=CCC(C)(C)c2cc(OCc3ccccc3)c(Br)cc21

nearest known ligand 0.40

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
CCR5 P51681 1/20 0.40
RAB9A P51151 3/20 0.39
ALDH1A1 P00352 1/20 0.39
HTR2A P28223 1/20 0.39
HTR2C P28335 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
PTPN1 P18031 3/20 0.38
SLC6A4 P31645 2/20 0.35
KDM4E B2RXH2 1/20 0.35
HPGD P15428 1/20 0.35
TLR9 Q9NR96 1/20 0.35
L3MBTL1 Q9Y468 2/20 0.34
MAPT P10636 1/20 0.34
MAPK1 P28482 1/20 0.34
TDP1 Q9NUW8 1/20 0.34
NPC1 O15118 1/20 0.34
ABCB1 P08183 1/20 0.34
HTR7 P34969 1/20 0.33
HTR6 P50406 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
SCHEMBL6086506 0.90 HTR7 (0.37) CCR5RAB9AALDH1A1SMN1; SMN2HPGD
SCHEMBL6086042 0.85 RAB9A (0.41) CCR5RAB9AALDH1A1HTR2AHTR2C
SCHEMBL6087079 0.83 HTR2A (0.32) HTR2AHTR2CHPGDL3MBTL1MAPT
SCHEMBL6086402 0.82 RAB9A (0.41) CCR5RAB9AALDH1A1HTR2AHTR2C
SCHEMBL6086567 0.81 RXRA (0.31) HPGD
SCHEMBL6086974 0.80 PTPN1 (0.35) ALDH1A1PTPN1KDM4EHPGDL3MBTL1
SCHEMBL6477273 0.76 HTR2A (0.47) CCR5RAB9AALDH1A1HTR2AHTR2C
SCHEMBL6086323 0.75 POLB (0.44) KDM4EMAPT
SCHEMBL6086311 0.75 RXRA (0.47) RAB9ASMN1; SMN2HPGDMAPTNPC1
SCHEMBL6086318 0.74 POLB (0.44) KDM4EMAPT

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 4 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7026487-B2 Amines substituted with a dihydronaphthalenyl, chromenyl, or thiochromenyl group, a pyridyl group and an alkyl group, having retinoid-like biological activity ALLERGAN, INC. (US) 2006-04-11 US disclosed
US-20040097733-A1 Amines substituted with a dihydronaphthalenyl, chromenyl, or thiochromenyl group, an aryl or heteroaryl group and an alkyl group, having retinoid-like biological activity BEARD RICHARD L (US) 2004-05-20 US disclosed
US-20030166932-A1 Amines substituted with a dihydronaphthalenyl, chromenyl, or thiochromenyl group, an aryl or heteroaryl group and an alkyl group, having retinoid-like biological activity ALLERGAN SALES, INC. 2003-09-04 US disclosed
US-6613917-B1 Retinoid agonist, antagonist or negative hormone-like biological activity ALLERGAN, INC. 2003-09-02 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-20030166932-A1 Amines substituted with a dihydronaphthalenyl, chromenyl, or thiochromenyl group, an aryl or heteroaryl group and an alkyl group, having retinoid-like biological activity NR4A1, NR2E3, NR0B1 CCR5 2851/4885RAB9A 1352/4885ALDH1A1 242/4885
US-20040097733-A1 Amines substituted with a dihydronaphthalenyl, chromenyl, or thiochromenyl group, an aryl or heteroaryl group and an alkyl group, having retinoid-like biological activity NR4A1, NR2E3, NR0B1 CCR5 2851/4885RAB9A 1352/4885ALDH1A1 242/4885

“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.