Alcohol

Alcohol

SCHEMBL22129229

CCO.COCc1c(F)c(F)c(COC(C)=O)c(F)c1F

nearest known ligand 0.47

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

MMP1MMP13MMP7MMP8polrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Alcohol. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
MMP1 known ✓ P03956 1/20 0.33
CA2 P00918 1/20 0.39
ALDH1A1 P00352 6/20 0.37
LMNA P02545 1/20 0.37
HSD17B10 Q99714 1/20 0.37
MMP2 P08253 1/20 0.33
MMP9 P14780 1/20 0.33
MMP12 P39900 1/20 0.33
TDP1 Q9NUW8 1/20 0.32
TSHR P16473 1/20 0.31
GCGR P47871 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
SCHEMBL1785282 0.94 CA2 (0.42) CA2ALDH1A1LMNAHSD17B10MMP1
SCHEMBL44341 0.84 CA2 (0.46) CA2ALDH1A1LMNAHSD17B10MMP1
Alcohol SCHEMBL22160482 0.84 CYP1A2 (0.37) ALDH1A1HSD17B10MMP1MMP2MMP9
SCHEMBL22160484 0.82 CA2 (0.42) CA2ALDH1A1LMNAHSD17B10MMP1
SCHEMBL22160485 0.79 CYP1A2 (0.36) ALDH1A1HSD17B10MMP1MMP2MMP9
SCHEMBL1786267 0.79 MEN1 (0.43) CA2ALDH1A1LMNAHSD17B10MMP1
SCHEMBL22129223 0.79 MMP1 (0.36) ALDH1A1LMNAMMP1MMP2MMP9
SCHEMBL9785523 0.77 CA2 (0.41) CA2ALDH1A1LMNAHSD17B10MMP1
Acetic Acid SCHEMBL22129233 0.77 PRKCE (0.36) ALDH1A1TDP1GCGR
SCHEMBL27815858 0.76 ALDH1A1 (0.39) ALDH1A1HSD17B10MMP1MMP2MMP9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10745334-B2 Method for synthesizing 2,3,5,6-tetrafluoro-4-methoxymethyl benzyl alcohol ZHEJIANG ZHONGXIN FLUORIDE MAT CO LTD (CN) 2020-08-18 US disclosed
US-20200207693-A1 METHOD FOR SYNTHESIZING 2,3,5,6-TETRAFLUORO-4-METHOXYMETHYL BENZYL ALCOHOL ZHEJIANG ZHONGXIN FLUORIDE MAT CO LTD (CN) 2020-07-02 US disclosed
WO-2020124727-A1 SYNTHESIS METHOD FOR 2,3,5,6-TETRAFLUORO-4-METHOXYMETHYL BENZYL ALCOHOL 浙江中欣氟材股份有限公司 2020-06-25 WO 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-10745334-B2 Method for synthesizing 2,3,5,6-tetrafluoro-4-methoxymethyl benzyl alcohol TET2, TH, ALKBH2 MMP1 3686/4885CA2 1199/4885ALDH1A1 362/4885
US-20200207693-A1 METHOD FOR SYNTHESIZING 2,3,5,6-TETRAFLUORO-4-METHOXYMETHYL BENZYL ALCOHOL TH, ALKBH2, ALKBH3 MMP1 3587/4885CA2 1650/4885ALDH1A1 345/4885

“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.