Formic Acid

Formic Acid

SCHEMBL2806812

COC(=O)[C@H](O)[C@@H](N)c1ccccc1.O=CO

nearest known ligand 0.56

Full drug profile on Sugi Atlas →

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 4/20 0.56
PTGS1 P23219 1/20 0.43
PTGS2 P35354 1/20 0.43
LTA4H P09960 1/20 0.43
CYP3A4 P08684 1/20 0.41
CYP1A2 P05177 1/20 0.41
CYP2D6 P10635 1/20 0.41
TSHR P16473 1/20 0.41
MAPK1 P28482 1/20 0.41
HSD17B10 Q99714 1/20 0.41
DPP4 P27487 2/20 0.41
MEN1 O00255 2/20 0.40
ALDH1A1 P00352 1/20 0.40
LMNA P02545 1/20 0.40
ADRA2A P08913 1/20 0.38
ADRA2C P18825 1/20 0.38

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
SCHEMBL487429 0.93 KMT2A (0.58) KMT2APTGS1PTGS2LTA4HCYP3A4
SCHEMBL12067910 0.93 KMT2A (0.58) KMT2APTGS1PTGS2LTA4HCYP3A4
SCHEMBL4731036 0.93 KMT2A (0.58) KMT2APTGS1PTGS2LTA4HCYP3A4
Hydrochloric Acid SCHEMBL27549891 0.92 KMT2A (0.56) KMT2APTGS1PTGS2LTA4HCYP3A4
Ammonia Solution, Strong SCHEMBL6349111 0.92 KMT2A (0.56) KMT2APTGS1PTGS2LTA4HCYP3A4
Hydrochloric Acid SCHEMBL6427164 0.92 KMT2A (0.56) KMT2APTGS1PTGS2LTA4HCYP3A4
Acetic Acid SCHEMBL27782195 0.90 KMT2A (0.55) KMT2APTGS1PTGS2LTA4HCYP3A4
Acetic Acid SCHEMBL487399 0.90 KMT2A (0.55) KMT2APTGS1PTGS2LTA4HCYP3A4
SCHEMBL27565933 0.80 DPP4 (0.43) KMT2ACYP1A2CYP2D6MAPK1DPP4
Mandelic Acid, Methyl Ester SCHEMBL30951860 0.80 KMT2A (0.63) KMT2APTGS1PTGS2CYP2D6MAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2108014-A1 METHOD OF PREPARING DOCETAXEL AND INTERMEDIATES USED THEREIN Hanmi Pharm. Co., Ltd. (KR) 2009-10-14 EP claimed
WO-2008072849-A1 METHOD OF PREPARING DOCETAXEL AND INTERMEDIATES USED THEREIN HANMI PHARM. CO., LTD. (KR) 2008-06-19 WO claimed
US-20100099896-A1 METHOD OF PREPARING DOCETAXEL AND INTERMEDIATES USED THEREIN HANMI PHARM. CO. LTD (KR) 2010-04-22 US disclosed
EP-2108014-A1 METHOD OF PREPARING DOCETAXEL AND INTERMEDIATES USED THEREIN Hanmi Pharm. Co., Ltd. (KR) 2009-10-14 EP disclosed
WO-2008072849-A1 METHOD OF PREPARING DOCETAXEL AND INTERMEDIATES USED THEREIN HANMI PHARM. CO., LTD. (KR) 2008-06-19 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 (1 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-20100099896-A1 METHOD OF PREPARING DOCETAXEL AND INTERMEDIATES USED THEREIN MCL1, DPYD, THPO KMT2A 3620/4885PTGS1 2625/4885PTGS2 2558/4885

“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.