Teichomycin A2 factor 2 (CED0002875)

Record Information

Version

1.0

Creation Date

2026-03-31 21:13:38 UTC

Update Date

2026-05-20 19:29:47 UTC

Accession Number

CHEM057979

Identification

Common Name

Teichomycin A2 factor 2

Class

Small Molecule

Description

Teichomycin A2 factor 2 belongs to the amino acids, peptides, and analogues, a subclass of carboxylic acids and derivatives within the organic compounds. With an average molecular weight of 1,880 g/mol, Teichomycin A2 factor 2 is a heavy molecule. It has the chemical formula C88H97Cl2N9O33. This compound is found in or released from one recorded source: healthcare, pharmaceuticals & veterinary products (Antibiotics). Recorded exposure routes for this substance include inhalation and oral administration.

Contaminant Type

Not Available

Chemical Structure

MOL SDF PDB SMILES InChI

Synonyms

Not Available

Chemical Formula

C₈₈H₉₇Cl₂N₉O₃₃

Average Molecular Mass

1879.670 g/mol

Monoisotopic Mass

1877.557 g/mol

CAS Registry Number

91032-26-7

IUPAC Name

Not Available

Traditional Name

Not Available

SMILES

CC(C)CCCCCCC(=O)N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=C2OC3=CC=C(C[C@H]4NC(=O)[C@H](N)C5=CC(OC6=CC(=CC(O)=C6)[C@H](NC4=O)C(=O)N[C@@H]4C(C=C1OC1=C(Cl)C=C(C=C1)[C@@H](O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1NC(C)=O)[C@@H]1NC(=O)[C@H](NC4=O)C4=CC(=C(O)C=C4)C4=C(C=C(O)C=C4O[C@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]4O)[C@H](NC1=O)C(O)=O)=C2)=C(O)C=C5)C=C3Cl

InChI Identifier

InChI=1S/C88H97Cl2N9O33/c1-33(2)8-6-4-5-7-9-60(108)94-68-74(113)71(110)58(31-101)129-87(68)132-78-55-25-40-26-56(78)126-52-17-13-38(23-47(52)90)77(131-86-67(92-34(3)103)73(112)70(109)57(30-100)128-86)69-84(121)98-66(85(122)123)45-28-42(105)29-54(127-88-76(115)75(114)72(111)59(32-102)130-88)61(45)44-22-37(12-14-49(44)106)63(81(118)99-69)96-83(120)65(40)97-82(119)64-39-20-41(104)27-43(21-39)124-53-24-36(11-15-50(53)107)62(91)80(117)93-48(79(116)95-64)19-35-10-16-51(125-55)46(89)18-35/h10-18,20-29,33,48,57-59,62-77,86-88,100-102,104-107,109-115H,4-9,19,30-32,91H2,1-3H3,(H,92,103)(H,93,117)(H,94,108)(H,95,116)(H,96,120)(H,97,119)(H,98,121)(H,99,118)(H,122,123)/t48-,57-,58-,59-,62+,63-,64+,65-,66-,67-,68-,69+,70-,71-,72-,73-,74-,75+,76+,77-,86+,87+,88+/m1/s1

InChI Key

GHOXVFYORXUCPY-VPMXZCLFSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Oligopeptides

Alternative Parents

Substituents

Alpha-oligopeptide
Cyclic alpha peptide
Acylaminosugar
N-acyl-alpha-hexosamine
Phenolic glycoside
Alpha-amino acid amide
O-glycosyl compound
Glycosyl compound
Diaryl ether
Alpha-amino acid or derivatives
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Aralkylamine
N-acyl-amine
Monosaccharide
Oxane
Aryl chloride
Fatty amide
Aryl halide
Benzenoid
Fatty acyl
Acetamide
Secondary alcohol
Secondary carboxylic acid amide
Lactam
Amino acid
Carboxamide group
Carboxylic acid salt
Amino acid or derivatives
Acetal
Oxacycle
Azacycle
Organoheterocyclic compound
Carboxylic acid
Ether
Polyol
Monocarboxylic acid or derivatives
Organohalogen compound
Primary amine
Amine
Organic zwitterion
Organic salt
Organopnictogen compound
Organic oxygen compound
Alcohol
Carbonyl group
Organic nitrogen compound
Hydrocarbon derivative
Primary alcohol
Organic oxide
Primary aliphatic amine
Organooxygen compound
Organonitrogen compound
Organochloride
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Biological Properties

Status

Detected and Not Quantified

Origin

Not Available

Cellular Locations

Not Available

Biofluid Locations

Not Available

Tissue Locations

Not Available

Applications

Not Available

Biological Roles

Not Available

Chemical Roles

Not Available

Organoleptic Effects

Not Available

Physical Properties

State

Not Available

Appearance

Not Available

Experimental Properties

Property	Value
Melting Point	Not Available
Boiling Point	Not Available
Solubility	Not Available

Predicted Properties

Not Available

Spectra

Not Available

Toxicity Profile

Mechanism of Toxicity

Not Available

Carcinogenicity (IARC Classification)

Not Available

Minimum Risk Level

Not Available

Symptoms

Not Available

Treatment

Not Available

Toxicity Values

Not Available

Health Effects

Health Effect	Relationship	Direction	Reference

Exposure Sources

Source ID	Source	Sector	Reference
306	Antibiotics	Healthcare, pharmaceuticals & veterinary products	Not Available

Pathways

0 pathways

No pathways found

No metabolic pathways have been associated with this synthetic chemical

Targets

Structure	Protein	UniProt ID	Organism	Relationship	Details
Click to view 3D structure	UDP-N-acetylglucosamine--N-acetylmuramyl-(pentapeptide) pyrophosphoryl-undecaprenol N-acetylglucosamine transferase	P17443	Escherichia coli (strain K12)	Predicted (SEA)	0.0778492
Click to view 3D structure	Signal peptidase IB	P0A070	Staphylococcus aureus	Predicted (SEA)	1.24559
Click to view 3D structure	N-acetyllactosaminide alpha-1,3-galactosyltransferase	P50127	Sus scrofa	Predicted (SEA)	11.5995
Click to view 3D structure	CD44 antigen	P16070	Humans	Predicted (SEA)	6.15009
Click to view 3D structure	CD44 antigen	P15379	Mus musculus	Predicted (SEA)	6.15009
Click to view 3D structure	Alpha-2A adrenergic receptor	P08913	Humans	Predicted (SEA)	4490.27
Click to view 3D structure	Gag-Pol polyprotein	Q7ZJM1	Human immunodeficiency virus 1	Predicted (SEA)	1109.58
Click to view 3D structure	Carbonic anhydrase 12	O43570	Humans	Predicted (SEA)	3945.55
Click to view 3D structure	Beta-1,4-galactosyltransferase 1	P08037	Bos taurus	Predicted (SEA)	38.0683
Click to view 3D structure	Carbonic anhydrase 7	P43166	Humans	Predicted (SEA)	4145.24
Click to view 3D structure	Carbonic anhydrase 1	P00915	Humans	Predicted (SEA)	4964.44
Click to view 3D structure	Fanconi anemia group F protein	Q9NPI8	Humans	Predicted (SEA)	10.8989
Click to view 3D structure	Sodium/glucose cotransporter 1	P13866	Humans	Predicted (SEA)	137.871
Click to view 3D structure	Asialoglycoprotein receptor 1	P34927	Mus musculus	Predicted (SEA)	94.6646
Click to view 3D structure	Signal peptidase I	P00803	Escherichia coli (strain K12)	Predicted (SEA)	59.0097
Click to view 3D structure	Carbon storage regulator	P69913	Escherichia coli	Predicted (SEA)	238.141
Click to view 3D structure	Kallikrein 1	O97506	Sus scrofa	Predicted (SEA)	155.231
Click to view 3D structure	Sodium-dependent serotonin transporter	P31652	Rattus norvegicus	Predicted (SEA)	5259.03
Click to view 3D structure	Carbonic anhydrase 2	P00918	Humans	Predicted (SEA)	5885.56
Click to view 3D structure	Carbonic anhydrase 4	P22748	Humans	Predicted (SEA)	4213.12
Click to view 3D structure	Sodium/glucose cotransporter 2	P31639	Humans	Predicted (SEA)	179.754
Click to view 3D structure	Gamma-aminobutyric acid receptor subunit beta-1	P18505	Humans	Predicted (SEA)	151.027
Click to view 3D structure	Plasma kallikrein	P14272	Rattus norvegicus	Predicted (SEA)	177.496
Click to view 3D structure	Solute carrier organic anion transporter family member 1B1	Q9Y6L6	Humans	Predicted (SEA)	3011.83
Click to view 3D structure	Tumor necrosis factor receptor superfamily member 5	P25942	Humans	Predicted (SEA)	291.156