Mycophenolic Acid

Mycophenolic Acid

SCHEMBL1374332

COc1c(C)c2c(c(O)c1C/C=C(\C)CCC(=O)O)C(=O)OC2.Cl

nearest known ligand 0.98

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

IMPDH1IMPDH2

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ IMPDH2 known ✓ P12268 20/20 0.98
▸ IMPDH1 known ✓ P20839 10/20 0.98
▸ KDM4E B2RXH2 1/20 0.98
▸ ALDH1A1 P00352 1/20 0.98
▸ LMNA P02545 1/20 0.98
▸ CYP1A2 P05177 1/20 0.98
▸ CYP3A4 P08684 1/20 0.98
▸ HPGD P15428 1/20 0.98
▸ UGT2B7 P16662 1/20 0.98
▸ SMN1; SMN2 Q16637 1/20 0.98
▸ HSD17B10 Q99714 1/20 0.98
▸ HDAC3 O15379 2/20 0.78
▸ HDAC4 P56524 2/20 0.78
▸ HDAC1 Q13547 2/20 0.78
▸ HDAC7 Q8WUI4 2/20 0.78
▸ HDAC2 Q92769 2/20 0.78
▸ HDAC10 Q969S8 2/20 0.78
▸ HDAC11 Q96DB2 2/20 0.78
▸ HDAC8 Q9BY41 2/20 0.78
▸ HDAC6 Q9UBN7 2/20 0.78

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
Mycophenolic Acid SCHEMBL9185989 1.00 IMPDH2 (0.98) IMPDH2IMPDH1KDM4EALDH1A1LMNA
Mycophenolic Acid SCHEMBL1230249 0.99 IMPDH2 (1.00) IMPDH2IMPDH1KDM4EALDH1A1LMNA
Mycophenolic Acid SCHEMBL29645054 0.99 IMPDH2 (1.00) IMPDH2IMPDH1KDM4EALDH1A1LMNA
Mycophenolic Acid SCHEMBL5500098 0.99 IMPDH2 (1.00) IMPDH2IMPDH1KDM4EALDH1A1LMNA
Mycophenolic Acid SCHEMBL1657813 0.99 IMPDH2 (1.00) IMPDH2IMPDH1KDM4EALDH1A1LMNA
Mycophenolic Acid SCHEMBL2514376 0.99 IMPDH2 (1.00) IMPDH2IMPDH1KDM4EALDH1A1LMNA
Mycophenolic Acid SCHEMBL4549 0.99 IMPDH2 (1.00) IMPDH2IMPDH1KDM4EALDH1A1LMNA
Mycophenolic Acid SCHEMBL29380425 0.99 IMPDH2 (1.00) IMPDH2IMPDH1KDM4EALDH1A1LMNA
Mycophenolic Acid SCHEMBL5259872 0.99 IMPDH2 (1.00) IMPDH2IMPDH1KDM4EALDH1A1LMNA
Mycophenolic Acid SCHEMBL6502425 0.98 IMPDH2 (0.98) IMPDH2IMPDH1KDM4EALDH1A1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024038306-A1 DIRECT PREPARATION OF MYCOPHENOLATE MOFETIL IN ANISOLE AND SIMPLE, ONE- POT ISOLATION OF ITS PURE OXALATE SALT ALBORZ BULK PHARMACEUTICAL COMPANY (IR) 2024-02-22 — — WO disclosed
CN-109789225-A DNA MONOCLONAL ANTIBODIES TARGETING CHECKPOINT MOLECULES 宾夕法尼亚大学理事会 2019-05-21 — — CN disclosed
CN-107405321-A Use of short chain fatty acids in cancer prevention 坦普尔大学 2017-11-28 — — CN disclosed
CN-106236741-A For treating the Compounds and methods for of abnormal adrenal cortical cell disease 密歇根大学董事会 2016-12-21 — — CN disclosed
CN-104302283-B Compounds and methods for treating aberrant adrenocortical cell disorders 密歇根大学董事会 2016-08-24 — — CN disclosed
CN-105848680-A Treatment using bruton's tyrosine kinase inhibitors and immunotherapy 药品循环有限责任公司 2016-08-10 — — CN disclosed
US-9139604-B2 Antiviral phosphonate analogs GILEAD SCIENCES, INC. (US) 2015-09-22 — — US disclosed
US-20150025039-A1 ANTIVIRAL PHOSPHONATE ANALOGS GILEAD SCIENCES, INC. 2015-01-22 — — US disclosed
US-8871785-B2 Antiviral phosphonate analogs GILEAD SCIENCES, INC. (US) 2014-10-28 — — US disclosed
US-20130316969-A1 ANTIVIRAL PHOSPHONATE ANALOGS GILEAD SCIENCES, INC. (US) 2013-11-28 — — US disclosed
WO-2004096286-A2 ANTIVIRAL PHOSPHONATE ANALOGS GILEAD SCIENCES, INC. (US) 2004-11-11 — — WO disclosed
WO-2004096235-A2 ANTI-CANCER PHOSPHONATE ANALOGS GILEAD SCIENCES, INC. (US) 2004-11-11 — — WO disclosed
WO-2004096236-A2 IMMUNOMODULATOR PHOSPHONATE CONJUGATES GILEAD SCIENCES, INC. (US) 2004-11-11 — — WO disclosed
EP-1421081-A4 METHOD OF MYCOPHENOLATE MOFETIL PREPARATION IVAX CR A S (CZ) 2004-11-03 — — EP disclosed
EP-1421081-A1 METHOD OF MYCOPHENOLATE MOFETIL PREPARATION IVAX-CR a.s. (CZ) 2004-05-26 — — EP disclosed
WO-2002100855-A1 METHOD OF MYCOPHENOLATE MOFETIL PREPARATION IVAX CORPORATION (US) 2002-12-19 — — WO disclosed
EP-0670724-A1 USE OF MYCOPHENOLIC ACID, MYCOPHENOLATE MOFETIL OR DERIVATE THEREOF TO INHIBIT STENOSIS SYNTEX (U.S.A.) INC. (US) 1995-09-13 — — EP disclosed
WO-1994012184-A1 USE OF MYCOPHENOLIC ACID, MYCOPHENOLATE MOFETIL OR DERIVATE THEREOF TO INHIBIT STENOSIS SYNTEX (U.S.A.) INC. (US) 1994-06-09 — — WO disclosed
EP-0281713-B1 MORPHOLINOETHYLESTER OF MYCOPHENOLIC ACID AND DERIVATIVES THEREOF, THEIR PREPARATION AND USE IN PHARMACEUTICAL COMPOSITIONS SYNTEX (U.S.A.) INC. (US) 1991-10-09 — — EP disclosed
EP-0281713-A1 Morpholinoethylester of mycophenolic acid and derivatives thereof, their preparation and use in pharmaceutical compositions SYNTEX (U.S.A.) INC. (US) 1988-09-14 — — EP 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-20150025039-A1 ANTIVIRAL PHOSPHONATE ANALOGS TYMP, ITPA, PNP IMPDH2 246/4885IMPDH1 160/4885KDM4E 2471/4885
US-20130316969-A1 ANTIVIRAL PHOSPHONATE ANALOGS TYMP, ITPA, PNP IMPDH2 246/4885IMPDH1 160/4885KDM4E 2471/4885

“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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