Ammonia Solution, Strong

Ammonia Solution, Strong

SCHEMBL6779003

N.N.O=C(O)CC(CO)C(=O)O

nearest known ligand 0.54

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
FOLH1 Q04609 5/20 0.54
TDP1 Q9NUW8 2/20 0.52
SLC1A1 P43005 1/20 0.46
CPA1 P15085 2/20 0.45
CPB1 P15086 1/20 0.45
CPA3 P15088 1/20 0.45
CPB2 Q96IY4 1/20 0.45
SMN1; SMN2 Q16637 1/20 0.43
MME P08473 2/20 0.41
SLC22A6 Q4U2R8 1/20 0.41
OR51E2 Q9H255 1/20 0.39
CHRM1 P11229 1/20 0.36
AKR1A1 P14550 1/20 0.36
CHRM3 P20309 1/20 0.36
HTR2A P28223 1/20 0.36
HTR2C P28335 1/20 0.36
ADRA1A P35348 1/20 0.36
HRH1 P35367 1/20 0.36
DRD3 P35462 1/20 0.36
SLC6A3 Q01959 1/20 0.36

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
SCHEMBL542313 0.97 FOLH1 (0.56) FOLH1TDP1SLC1A1CPA1CPB1
SCHEMBL28920282 0.94 FOLH1 (0.54) FOLH1TDP1SLC1A1CPA1CPB1
Tricarballylic Acid SCHEMBL11291769 0.85 FOLH1 (0.62) FOLH1TDP1CPA1CPB1CPA3
Tricarballylic Acid SCHEMBL28692658 0.82 FOLH1 (0.59) FOLH1TDP1CPA1CPB1CPA3
Tricarballylic Acid SCHEMBL1821947 0.82 FOLH1 (0.65) FOLH1TDP1CPA1CPB1CPA3
Ammonia Solution, Strong SCHEMBL16760976 0.82
Tricarballylic Acid SCHEMBL34866 0.82 FOLH1 (0.65) FOLH1TDP1CPA1CPB1CPA3
Tricarballylic Acid SCHEMBL2462503 0.79 FOLH1 (0.62) FOLH1TDP1CPA1CPB1CPA3
Tricarballylic Acid SCHEMBL11736211 0.79 FOLH1 (0.62) FOLH1TDP1CPA1CPB1CPA3
Tricarballylic Acid SCHEMBL11728494 0.79 FOLH1 (0.62) FOLH1TDP1CPA1CPB1CPA3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115047084-A Use of blood lipids for milk product intake and disease prediction 中国科学院上海营养与健康研究所 2022-09-13 CN disclosed
US-11427869-B2 T cell balance gene expression, compositions of matters and methods of use thereof THE BROAD INSTITUTE, INC. (US) 2022-08-30 US disclosed
CN-114544924-A Application of glyceride in disease prediction 中国科学院上海营养与健康研究所 2022-05-27 CN disclosed
CN-114414668-A Use of sphingolipids for disease prediction 中国科学院上海营养与健康研究所 2022-04-29 CN disclosed
US-20210401953-A1 ASPARAGINASE THERAPEUTIC METHODS THE BROAD INSTITUTE, INC. (US) 2021-12-30 US disclosed
US-20200317767-A1 GROWTH DIFFERENTIATION FACTOR (GDF) FOR TREATMENT OF DIASTOLIC HEART FAILURE THE BRIGHAM AND WOMEN'S HOSPITAL, INC. (US) 2020-10-08 US disclosed
WO-2020102427-A1 ASPARAGINASE THERAPEUTIC METHODS THE BROAD INSTITUTE, INC. (US) 2020-05-22 WO disclosed
EP-2828289-B1 GROWTH DIFFERENTIATION FACTOR (GDF) 11 FOR TREATMENT OF AGE-RELATED CARDIOVASCULAR CONDITION BRIGHAM & WOMENS HOSPITAL INC (US) 2020-02-26 EP disclosed
US-10446259-B2 Systems, apparatus, and methods for analyzing and predicting cellular pathways MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2019-10-15 US disclosed
US-20180340022-A1 GROWTH DIFFERENTIATION FACTOR (GDF) FOR TREATMENT OF DIASTOLIC HEART FAILURE THE BRIGHAM AND WOMEN'S HOSPITAL, INC. (US) 2018-11-29 US disclosed
US-6706893-B2 BY HYDROGENATION OF STARTING MATERIALS INCLUDING SUCCINIC ACID, N-METHYLSUCCINIMIDE; EFFICIENCY BATTELLE MEMORIAL INSTITUTE 2004-03-16 US disclosed
US-6670483-B2 Catalytically hydrogenating n-methyl-succinimide to form n-methylpyrrolidone BATTELLE MEMORIAL INSTITUTE 2003-12-30 US disclosed
US-6632951-B2 Making N- methylpyrrolidine and analogous compounds via hydrogenation. Novel catalysts for this process, and novel conditions/yields are also described. Other process improvements may include extraction and hydrolysis steps. BATTELLE MEMORIAL INSTITUTE 2003-10-14 US disclosed
US-6603021-B2 Making pyrrolidones, especially N-methyl pyrrolidone (\"NMP\"), by hydrogenation of succinimides BATTELLE MEMORIAL INSTITUTE 2003-08-05 US disclosed
US-20030125570-A1 Methods of making pyrrolidones WERPY TODD (US) 2003-07-03 US disclosed
US-20030120087-A1 Methods of making pyrrolidones WERPY TODD (US) 2003-06-26 US disclosed
US-20030114687-A1 Methods of making pyrrolidones WERPY TODD (US) 2003-06-19 US disclosed
US-20030097006-A1 Methods of making pyrrolidones ENERGY, U.S. DEPARTMENT OF 2003-05-22 US disclosed
EP-0232736-A1 Preparation of 4'-aminomethylfluorescein derivatives for use in fluorescence polarization immunoassays ABBOTT LABORATORIES (US) 1987-08-19 EP disclosed
EP-0201751-A2 4'-aminomethyfluorescein derivatives for use in fluorescence polarization immunoassys ABBOTT LABORATORIES (US) 1986-11-20 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 (4 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-20030120087-A1 Methods of making pyrrolidones HPD, HNMT, DHPS FOLH1 743/4885TDP1 1179/4885SLC1A1 2126/4885
US-20030125570-A1 Methods of making pyrrolidones HPD, HNMT, DHPS FOLH1 743/4885TDP1 1179/4885SLC1A1 2126/4885
US-20030114687-A1 Methods of making pyrrolidones HPD, HNMT, DHPS FOLH1 743/4885TDP1 1179/4885SLC1A1 2126/4885
US-20030097006-A1 Methods of making pyrrolidones HPD, HNMT, DHPS FOLH1 743/4885TDP1 1179/4885SLC1A1 2126/4885

“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.