Phenol

Phenol

SCHEMBL1793331

C1CCNC1.Oc1ccccc1

nearest known ligand 0.58

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CA12 O43570 1/20 0.58
▸ CA1 P00915 1/20 0.58
▸ CA2 P00918 1/20 0.58
▸ GLA P06280 1/20 0.58
▸ CA3 P07451 1/20 0.58
▸ CA4 P22748 1/20 0.58
▸ CA9 Q16790 1/20 0.58
▸ TDP1 Q9NUW8 1/20 0.58
▸ CA14 Q9ULX7 1/20 0.58
▸ DRD2 P14416 2/20 0.42
▸ DRD1 P21728 2/20 0.42
▸ DRD4 P21917 1/20 0.42
▸ DRD5 P21918 1/20 0.42
▸ DRD3 P35462 1/20 0.42
▸ MMP3 P08254 1/20 0.42
▸ BCL2L1 Q07817 1/20 0.42
▸ ALDH1A1 P00352 1/20 0.40
▸ HTR2C P28335 1/20 0.40
▸ SIGMAR1 Q99720 3/20 0.39
▸ OPRM1 P35372 1/20 0.39

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
Phenol SCHEMBL5875014 0.97 CA12 (0.55) CA12CA1CA2GLACA3
Phenol SCHEMBL29140824 0.95 CA12 (0.52) CA12CA1CA2GLACA3
Phenol SCHEMBL28163778 0.95 CA12 (0.52) CA12CA1CA2GLACA3
Phenol SCHEMBL27919347 0.92 CA12 (0.69) CA12CA1CA2GLACA3
Phenol SCHEMBL5874295 0.89 CA12 (0.65) CA12CA1CA2GLACA3
Phenol SCHEMBL10791210 0.89 CA12 (0.65) CA12CA1CA2GLACA3
Phenol SCHEMBL10791213 0.89 CA12 (0.65) CA12CA1CA2GLACA3
Phenol SCHEMBL27280139 0.86 CA12 (0.61) CA12CA1CA2GLACA3
Phenol SCHEMBL28217458 0.86 CA12 (0.61) CA12CA1CA2GLACA3
Hydroquinone SCHEMBL11763246 0.86 ALDH1A1 (0.50) CA12CA1CA2CA3CA4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111018901-B Zanamivir and ranamivir intermediate and synthesis method thereof 中国科学院上海有机化学研究所 2021-09-03 — — CN claimed
CN-111116567-A Zanamivir and ranamivir intermediate and synthesis method thereof 中国科学院上海有机化学研究所 2020-05-08 — — CN claimed
CN-111018901-A Zanamivir and ranamivir intermediate and synthesis method thereof 中国科学院上海有机化学研究所 2020-04-17 — — CN claimed
CN-104418876-B Zanamivir and ranamivir intermediate and synthesis method thereof 中国科学院上海有机化学研究所 2019-05-17 — — CN claimed
CN-111116567-B Zanamivir and ranamivir intermediates and synthesis method thereof 中国科学院上海有机化学研究所 2023-10-10 — — CN disclosed
CN-111116533-B Zanamivir and ranamivir intermediate and synthesis method thereof 中国科学院上海有机化学研究所 2022-11-22 — — CN disclosed
CN-114213425-A Preparation process of carboxyl-X-rhodamine 合肥华纳生物医药科技有限公司 2022-03-22 — — CN disclosed
CN-114213425-A Preparation process of carboxyl-X-rhodamine 合肥华纳生物医药科技有限公司 2022-03-22 — — CN disclosed
CN-111018901-B Zanamivir and ranamivir intermediate and synthesis method thereof 中国科学院上海有机化学研究所 2021-09-03 — — CN disclosed
US-20210017211-A1 OLIGOSACCHARIDE C-GLYCOSIDE DERIVATIVES OKINAWA INSTITUTE OF SCIENCE AND TECHNOLOGY SCHOOL CORPORATION (JP) 2021-01-21 — — US disclosed
US-7951793-B2 Substituted heterocyclic derivatives useful as antidiabetic and antiobesity agents and method BRISTOL-MYERS SQUIBB COMPANY (US) 2011-05-31 — — US disclosed
EP-1656368-A4 SUBSTITUTED HERTOCYCLIC DERIVATIVES USEFUL AS ANTIDIABETIC AND ANTIOBESITY AGENTS AND METHOD BRISTOL MYERS SQUIBB CO (US) 2009-08-26 — — EP disclosed
US-20070287713-A1 SUBSTITUTED HETEROCYCLIC DERIVATIVES USEFUL AS ANTIDIABETIC AND ANTIOBESITY AGENTS AND METHOD BRISTOL-MYERS SQUIBB COMPANY 2007-12-13 — — US disclosed
US-7279485-B2 Substituted heterocyclic derivatives useful as antidiabetic and antiobesity agents and method BRISTOL-MYERS SQUIBB COMPANY (US) 2007-10-09 — — US disclosed
EP-1656368-A2 SUBSTITUTED HERTOCYCLIC DERIVATIVES USEFUL AS ANTIDIABETIC AND ANTIOBESITY AGENTS AND METHOD Bristol-Myers Squibb Company (US) 2006-05-17 — — EP disclosed
US-20040063700-A1 Substituted heterocyclic derivatives useful as antidiabetic and antiobesity agents and method BRISTOL-MYERS SQUIBB COMPANY 2004-04-01 — — US disclosed
WO-2004004665-A2 SUBSTITUTED HETEROCYCLIC DERIVATIVES USEFUL AS ANTIDIABETIC AND ANTIOBESITY AGENTS AND METHOD BRISTOL-MYERS SQUIBB COMPANY (US) 2004-01-15 — — WO disclosed
US-6458787-B1 NOVEL PYRROLIDINE COMPOUNDS THAT ARE POTENT AND SELECTIVE INHIBITORS OF PDE4, AS WELL AS METHODS OF MAKING THE SAME, ARE DISCLOSED. USE OF THE COMPOUNDS IN THE TREATMENT OF INFLAMMATORY DISEASES AND OTHER DISEASES INVOLVING ELEVATED ICOS CORPORATION 2002-10-01 — — US disclosed
US-6258833-B1 ENZYME INHIBITORS AND ANTIINFLAMMATORY AGENTS ICOS CORPORATION 2001-07-10 — — 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 (3 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-20070287713-A1 SUBSTITUTED HETEROCYCLIC DERIVATIVES USEFUL AS ANTIDIABETIC AND ANTIOBESITY AGENTS AND METHOD PYM1, GPR119, GLP1R CA12 2479/4885CA1 2862/4885CA2 877/4885
US-20210017211-A1 OLIGOSACCHARIDE C-GLYCOSIDE DERIVATIVES OSTC, FUT6, FUT5 CA12 155/4885CA1 1659/4885CA2 3004/4885
US-20040063700-A1 Substituted heterocyclic derivatives useful as antidiabetic and antiobesity agents and method GPR119, SLC5A2, GLP1R CA12 2448/4885CA1 3042/4885CA2 720/4885

“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.

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